PAZOPANIB- pazopanib hydrochloride tablet, film coated

pazopanib by

Drug Labeling and Warnings

pazopanib by is a Prescription medication manufactured, distributed, or labeled by Novugen Pharma (USA) LLC., Novugen Oncology Sdn. Bhd., Teyro Labs Private Limited. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

  • BOXED WARNING (What is this?)

    WARNING: HEPATOTOXICITY

    Severe and fatal hepatotoxicity has been observed in clinical trials. Monitor hepatic function and interrupt, reduce, or discontinue dosing as recommended[see Warnings and Precautions (5.1)].

  • 1 INDICATIONS AND USAGE

    1.1 Renal Cell Carcinoma

    Pazopanib tablets are indicated for the treatment of adults with advanced renal cell carcinoma (RCC).

    1.2 Soft Tissue Sarcoma

    Pazopanib tablets are indicated for the treatment of adults with advanced soft tissue sarcoma (STS) who have received prior chemotherapy.

    Limitations of Use: The efficacy of pazopanib tablets for the treatment of patients with adipocytic STS or gastrointestinal stromal tumors has not been demonstrated.

  • 2 DOSAGE AND ADMINISTRATION

    2.1 Recommended Dosage

    The recommended dosage of pazopanib tablets is 800 mg (four 200 mg tablets) orally once daily without food (at least 1 hour before or 2 hours after a meal) until disease progression or unacceptable toxicity [see Clinical Pharmacology (12.3)] . The dosage should be modified for hepatic impairment and in patients taking certain concomitant drugs [see Dosage and Administration (2.3, 2.4)] .

    Swallow tablets whole. Do not crush tablets due to the potential for increased rate of absorption, which may affect systemic exposure [see Clinical Pharmacology (12.3)] .

    If a dose is missed, it should not be taken if it is < 12 hours until the next dose.

    2.2 Dosage Modifications for Adverse Reactions

    Table 1 summarizes the recommended dose reductions.

    Table 1. Recommended Dose Reductions of Pazopanib Tablets for Adverse Reactions
    Dose reductionFor renal cell carcinomaFor soft tissue sarcoma
    First400 mg orally once daily600 mg orally once daily
    Second200 mg orally once daily400 mg orally once daily

    Permanently discontinue pazopanib tablets in patients unable to tolerate the second dose reduction.

    Table 2 summarizes the recommended dosage modifications for adverse reactions.

    Table 2. Recommended Dosage Modifications of Pazopanib Tablets for Adverse Reactions
    Abbreviations: ALT, alanine aminotransferase; ULN, upper limit of normal.
    aNational Cancer Institute Common Terminology Criteria for Adverse Events, version 5.
    Adverse reactionSeverity aDosage modification
    Hepatic Toxicity [see Warnings and Precautions (5.1)] Isolated ALT elevations between 3 × ULN and 8 × ULNContinue and monitor liver function weekly until ALT returns to Grade 1 or baseline.
    Isolated ALT elevations of > 8 × ULNWithhold until improvement to Grade 1 or baseline. If the potential benefit for resuming treatment with pazopanib tablets is considered to outweigh the risk for hepatotoxicity, then resume at a reduced dose of no more than 400 mg once daily and measure serum liver tests weekly for 8 weeks.

    Permanently discontinue if ALT elevations > 3 × ULN recur despite dose reduction(s).
    ALT elevations > 3 × ULN occur concurrently with bilirubin elevations > 2 × ULNPermanently discontinue and continue to monitor until resolution.

    Patients with only a mild, indirect (unconjugated) hyperbilirubinemia, known as Gilbert’s syndrome, and ALT elevations > 3 × ULN should be managed per the recommendations outlined for isolated ALT elevations.
    Left Ventricular Systolic Dysfunction [see Warnings and Precautions (5.3)] Symptomatic or Grade 3Withhold until improvement to Grade < 3. Resume treatment based on medical judgement.
    Grade 4Permanently discontinue.
    Hemorrhagic Events [see Warnings and Precautions (5.4)] Grade 2Withhold until improvement to Grade ≤ 1. Resume at reduced dose (see Table 1).

    Permanently discontinue if Grade 2 recurs after dose interruption and reduction.
    Grade 3 or Grade 4Permanently discontinue.
    Arterial Thromboembolic Events [see Warnings and Precautions (5.5)] Any gradePermanently discontinue.
    Venous Thromboembolic Events [see Warnings and Precautions (5.6)] Grade 3Withhold pazopanib tablets and resume at same dose if managed with appropriate therapy for at least one week.
    Grade 4Permanently discontinue.
    Thrombotic Microangiopathy [see Warnings and Precautions (5.7)] Any gradePermanently discontinue.
    Gastrointestinal Perforation [see Warnings and Precautions (5.8)] Any gradePermanently discontinue.
    Gastrointestinal Fistula [see Warnings and Precautions (5.8)] Grade 2 or Grade 3Withhold and resume based on medical judgement.
    Grade 4Permanently discontinue.
    Interstitial Lung Disease / Pneumonitis [see Warnings and Precautions (5.9)] Any gradePermanently discontinue.
    Posterior Reversible Encephalopathy Syndrome [see Warnings and Precautions (5.10)] Any gradePermanently discontinue.
    Hypertension [see Warnings and Precautions (5.11)] Grade 2 or Grade 3Reduce dose (see Table 1) and initiate or adjust anti-hypertensive therapy. Permanently discontinue if hypertension remains Grade 3 despite dose reduction(s) and adjustment of anti-hypertensive therapy.
    Grade 4 or hypertensive crisisPermanently discontinue.
    Proteinuria [see Warnings and Precautions (5.14)] 24-hour urine protein ≥ 3 gramsWithhold until improvement to Grade ≤ 1. Resume at a reduced dose (see Table 1).

    Permanently discontinue if 24-hour urine protein ≥ 3 grams does not improve or recurs despite dose reductions.
    Confirmed nephrotic syndromePermanently discontinue.

    2.3 Dosage Modifications for Hepatic Impairment

    Moderate and Severe Hepatic Impairment

    In patients with moderate hepatic impairment [total bilirubin > 1.5 to 3 × upper limit of normal (ULN) and any alanine aminotransferase (ALT) value], consider alternatives to pazopanib tablets. If pazopanib tablets are used in patients with moderate hepatic impairment, reduce the pazopanib tablets dose to 200 mg orally once daily.

    Pazopanib tablets are not recommended in patients with severe hepatic impairment (total bilirubin > 3 × ULN and any ALT value) [see Use in Specific Populations (8.7)] .

    2.4 Dosage Modifications for Drug Interactions

    Strong CYP3A4 Inhibitors

    Avoid concomitant use of strong CYP3A4 inhibitors by use of an alternate concomitant medication with no or minimal potential to inhibit CYP3A4. If co-administration of a strong CYP3A4 inhibitor is warranted, reduce the dose of pazopanib tablets to 400 mg [see Drug Interactions (7.1)] .

    Strong CYP3A4 Inducers

    Avoid concomitant use of strong CYP3A4 inducers by use of an alternate concomitant medication with no or minimal enzyme induction potential. Pazopanib tablets are not recommended in patients who cannot avoid chronic use of strong CYP3A4 inducers [see Drug Interactions (7.1)] .

    Gastric Acid-Reducing Agents

    Avoid concomitant use of gastric acid-reducing agents. If concomitant use of a gastric acid-reducing agent cannot be avoided, consider short-acting antacid in place of proton pump inhibitors (PPIs) and H2-receptor antagonists. Separate short-acting antacid and pazopanib tablets dosing by several hours [see Drug Interactions (7.4), Clinical Pharmacology (12.3)] .

  • 3 DOSAGE FORMS AND STRENGTHS

    Pazopanib tablets: 200 mg, gray, modified capsule-shaped, film-coated tablets debossed with “P 200” on one side and plain on the other side.

  • 4 CONTRAINDICATIONS

    None.

  • 5 WARNINGS AND PRECAUTIONS

    5.1 Hepatic Toxicity

    Hepatotoxicity, manifested as increases in ALT, aspartate aminotransferase (AST) and bilirubin, occurred in patients who received pazopanib. This hepatotoxicity can be severe and fatal. Patients older than 65 years are at greater risk for hepatotoxicity [see Use in Specific Populations (8.5)] . Transaminase elevations occur early in the course of treatment; 92% of all transaminase elevations of any grade occurred in the first 18 weeks.

    In the randomized RCC trial (VEG105192), ALT > 3 × ULN occurred in 18% and ALT > 10 × ULN occurred in 4% of the 290 patients who received pazopanib. Concurrent elevation in ALT > 3 × ULN and bilirubin > 2 × ULN in the absence of significant alkaline phosphatase > 3 × ULN occurred in 2%. In the monotherapy trials, 2 patients died with disease progression and hepatic failure.

    In the randomized STS trial (VEG110727), ALT > 3 × ULN occurred in 18% and ALT > 8 × ULN occurred in 5% of the 240 patients who received pazopanib. Concurrent elevation in ALT > 3 × ULN and bilirubin > 2 × ULN in the absence of significant alkaline phosphatase > 3 × ULN occurred in 2%. One patient died of hepatic failure.

    Monitor liver tests at baseline; at weeks 3, weeks 5, weeks 7, and weeks 9; at month 3 and month 4; and then periodically as clinically indicated. Increase to weekly monitoring for patients with elevated ALT until ALT returns to Grade 1 or baseline. Withhold pazopanib and resume at reduced dose with continued weekly monitoring for 8 weeks, or permanently discontinue with weekly monitoring until resolution based on severity of hepatotoxicity [see Dosage and Administration (2.2)].

    Gilbert’s Syndrome

    Pazopanib is a uridine diphosphate (UDP)-glucuronosyl transferase 1A1 (UGT1A1) inhibitor. Mild, indirect (unconjugated) hyperbilirubinemia may occur in patients with Gilbert’s syndrome [see Clinical Pharmacology (12.5)] . In patients with only a mild indirect hyperbilirubinemia known as Gilbert’s syndrome, manage elevation in ALT > 3 × ULN per the recommendations outlined for isolated ALT elevations [see Dosage and Administration (2.2)] .

    Concomitant Use of Simvastatin

    Concomitant use of pazopanib and simvastatin increases the risk of ALT elevations [see Drug Interactions (7.3)] . Insufficient data are available to assess the risk of concomitant administration of alternative statins and pazopanib.

    5.2 QT Prolongation and Torsades de Pointes

    In the RCC trials, 558/586 patients were subject to routine electrocardiogram (ECG) monitoring and QT prolongation ≥ 500 msec was identified in 2% of these 558 patients. In monotherapy trials, torsades de pointes occurred in < 1% of 977 patients who received pazopanib.

    In the randomized RCC (VEG105192) and STS (VEG110727) trials, 1% (3/290) and 0.4% (1/240) of patients, respectively, who received pazopanib had post-baseline values between 500 msec to 549 msec. Post-baseline QT data were only collected in the STS trial if ECG abnormalities were reported as an adverse reaction.

    Monitor patients who are at significant risk of developing QTc prolongation, including patients with a history of QT interval prolongation, in patients taking antiarrhythmics or other medications that may prolong QT interval, and those with relevant pre-existing cardiac disease [see Drug Interactions (7.5)] . Monitor ECG and electrolytes (e.g., calcium, magnesium, potassium) at baseline and as clinically indicated. Correct hypokalemia, hypomagnesemia, and hypocalcemia prior to initiating pazopanib and during treatment.

    5.3 Cardiac Dysfunction

    Cardiac dysfunction, including decreased left ventricular ejection fraction (LVEF) and congestive heart failure, occurred in patients who received pazopanib.

    In the RCC trials, cardiac dysfunction was observed in 0.6% of 586 patients without routine on-study LVEF monitoring. In the randomized RCC trial (VEG105192), myocardial dysfunction was defined as symptoms of cardiac dysfunction or ≥ 15% absolute decline in LVEF compared with baseline or a decline in LVEF of ≥ 10% compared with baseline that is also below the lower limit of normal. In an RCC trial (COMPARZ), myocardial dysfunction occurred in 13% of the 362 patients on pazopanib who had a baseline and post-baseline LVEF measurements. Congestive heart failure occurred in 0.5% of patients.

    In the randomized STS trial (VEG110727), myocardial dysfunction occurred in 11% of the 142 patients who had a baseline and a post-baseline LVEF measurements. One percent (3/240) of patients who received pazopanib had congestive heart failure, which did not resolve in one patient. Fourteen of the 16 patients with myocardial dysfunction treated with pazopanib had concurrent hypertension which may have exacerbated cardiac dysfunction in patients at risk (e.g., those with prior anthracycline therapy) possibly by increasing cardiac afterload.

    Monitor blood pressure and manage as appropriate [see Warnings and Precautions (5.11)] . Monitor for clinical signs or symptoms of congestive heart failure. Conduct baseline and periodic evaluation of LVEF in patients at risk of cardiac dysfunction, including previous anthracycline exposure. Withhold or permanently discontinue pazopanib based on severity of cardiac dysfunction [see Dosage and Administration (2.2)] .

    5.4 Hemorrhagic Events

    In the RCC trials, fatal hemorrhage occurred in 0.9% of 586 patients, and cerebral/intracranial hemorrhage was observed in < 1% (2/586) of patients treated with pazopanib.

    In the randomized RCC trial (VEG105192), 13% of 290 patients treated with pazopanib experienced at least 1 hemorrhagic event. The most common hemorrhagic events were hematuria (4%), epistaxis (2%), hemoptysis (2%), and rectal hemorrhage (1%). Nine of 37 patients treated with pazopanib who had hemorrhagic events experienced serious events, including pulmonary, gastrointestinal, and genitourinary hemorrhage. One percent of patients treated with pazopanib died from hemorrhage.

    In the randomized STS trial (VEG110727), 22% of 240 patients treated with pazopanib experienced at least 1 hemorrhagic event. The most common hemorrhagic events were epistaxis (8%), mouth hemorrhage (3%), and anal hemorrhage (2%). Grade 4 hemorrhagic events occurred in 1% of patients and included intracranial hemorrhage, subarachnoid hemorrhage, and peritoneal hemorrhage.

    Pazopanib has not been studied in patients who have a history of hemoptysis, cerebral hemorrhage, or clinically significant gastrointestinal hemorrhage in the past 6 months. Withhold pazopanib and resume at reduced dose or permanently discontinue based on severity of hemorrhagic events [see Dosage and Administration (2.2)] .

    5.5 Arterial Thromboembolic Events

    In the RCC trials, fatal arterial thromboembolic events occurred in 0.3% of 586 patients. In the randomized RCC trial (VEG105192), 2% of 290 patients who received pazopanib experienced myocardial infarction or ischemia, 0.3% had a cerebrovascular accident, and 1% had an event of transient ischemic attack.

    In the randomized STS trial (VEG110727), 2% of 240 patients who received pazopanib experienced a myocardial infarction or ischemia and 0.4% had a cerebrovascular accident.

    Pazopanib has not been studied in patients who have had an arterial thromboembolic event within the previous 6 months. Permanently discontinue pazopanib in case of an arterial thromboembolic event [see Dosage and Administration (2.2)] .

    5.6 Venous Thromboembolic Events

    Venous thromboembolic events (VTEs), including venous thrombosis and fatal pulmonary embolus (PE), occurred in patients who received pazopanib.

    In the randomized RCC trial (VEG105192), VTEs occurred in 1% of 290 patients who received pazopanib. In the randomized STS trial (VEG110727), VTEs were reported in 5% of 240 patients who received pazopanib. Fatal PE occurred in 1% (2/240).

    Monitor for signs and symptoms of VTE and PE. Withhold pazopanib and then resume at same dose or permanently discontinue based on severity of VTE [see Dosage and Administration (2.2)] .

    5.7 Thrombotic Microangiopathy

    Thrombotic microangiopathy (TMA), including thrombotic thrombocytopenic purpura (TTP) and hemolytic uremic syndrome (HUS), occurred in clinical trials of pazopanib as monotherapy, in combination with bevacizumab, and in combination with topotecan. Pazopanib is not indicated for use in combination with other agents. Six of the 7 TMA cases occurred within 90 days of the initiation of pazopanib. Improvement of TMA was observed after treatment was discontinued.

    Monitor for signs and symptoms of TMA. Permanently discontinue pazopanib in patients developing TMA. Manage as clinically indicated.

    5.8 Gastrointestinal Perforation and Fistula

    In the RCC and STS trials, gastrointestinal perforation or fistula occurred in 0.9% of 586 patients and 1% of 382 patients who received pazopanib, respectively. Fatal perforations occurred in 0.3% (2/586) of these patients in the RCC trials and in 0.3% (1/382) of these patients in the STS trials.

    Monitor for signs and symptoms of gastrointestinal perforation or fistula. Withhold pazopanib in case of Grade 2 or Grade 3 gastrointestinal fistula and resume based on medical judgement. Permanently discontinue pazopanib in case of gastrointestinal perforation or Grade 4 gastrointestinal fistula [see Dosage and Administration (2.2)] .

    5.9 Interstitial Lung Disease/Pneumonitis

    Interstitial lung disease (ILD)/pneumonitis, which can be fatal, has been reported with pazopanib across clinical trials. ILD/pneumonitis occurred in 0.1% of patients treated with pazopanib.

    Monitor patients for pulmonary symptoms indicative of ILD/pneumonitis. Permanently discontinue pazopanib in patients who develop ILD or pneumonitis [see Dosage and Administration (2.2)] .

    5.10 Posterior Reversible Encephalopathy Syndrome

    Posterior Reversible Encephalopathy Syndrome (PRES) has been reported in patients who received pazopanib and may be fatal. PRES is a neurological disorder which can present with headache, seizure, lethargy, confusion, blindness, and other visual and neurologic disturbances. Mild to severe hypertension may be present. Confirm diagnosis of PRES by magnetic resonance imaging.

    Permanently discontinue pazopanib in patients who develop PRES.

    5.11 Hypertension

    Hypertension (systolic blood pressure ≥ 150 mmHg or diastolic blood pressure ≥ 100 mmHg) and hypertensive crisis were observed in patients treated with pazopanib.

    Approximately 40% of patients who received pazopanib experienced hypertension, with Grade 3 occurring in 4% to 7% of patients [see Adverse Reactions (6.1)] . About 40% of cases occurred by Day 9 and about 90% of cases occurred in the first 18 weeks across clinical trials. Approximately 1% of patients required permanent discontinuation of pazopanib because of hypertension.

    Do not initiate pazopanib in patients with uncontrolled hypertension. Optimize blood pressure prior to initiating pazopanib. Monitor blood pressure as clinically indicated and initiate and adjust antihypertensive therapy as appropriate. Withhold and then dose reduce pazopanib or permanently discontinue based on severity of hypertension [see Dosage and Administration (2.2)] .

    5.12 Risk of Impaired Wound Healing

    Impaired wound healing complications can occur in patients who receive drugs that inhibit the vascular endothelial growth factor (VEGF) signaling pathway. Therefore, pazopanib has the potential to adversely affect wound healing.

    Withhold pazopanib at least 1 week prior to elective surgery. Do not administer for at least 2 weeks following major surgery and until adequate wound healing. The safety of resumption of pazopanib after resolution of wound healing complications has not been established.

    5.13 Hypothyroidism

    Hypothyroidism, confirmed based on a simultaneous rise of TSH and decline of T4, occurred in 7% of 290 patients who received pazopanib in the randomized RCC trial (VEG105192) and in 5% of 240 patients who received pazopanib in the randomized STS trial (VEG110727). Hypothyroidism occurred in 4% of the 586 patients in the RCC trials and 5% of the 382 patients in the STS trials.

    Monitor thyroid tests at baseline, during treatment and as clinically indicated and manage hypothyroidism as appropriate.

    5.14 Proteinuria

    In the randomized RCC trial (VEG105192), proteinuria occurred in 9% of 290 patients who received pazopanib. In 2 patients, proteinuria led to discontinuation of pazopanib.

    In the randomized STS trial (VEG110727), proteinuria occurred in 1% of 240 patients and nephrotic syndrome occurred in 1 patient. Treatment was discontinued in the patient with nephrotic syndrome.

    Perform baseline and periodic urinalysis during treatment with follow up measurement of 24-hour urine protein as clinically indicated. Withhold pazopanib then resume at a reduced dose or permanently discontinue based on severity of proteinuria. Permanently discontinue in patients with nephrotic syndrome [see Dosage and Administration (2.2)] .

    5.15 Tumor Lysis Syndrome

    Cases of tumor lysis syndrome (TLS), including fatal cases, have been reported in RCC and STS patients treated with pazopanib [see Adverse Reactions (6.2)] . Patients may be at risk of TLS if they have rapidly growing tumors, a high tumor burden, renal dysfunction, or dehydration. Closely monitor patients at risk, consider appropriate prophylaxis, and treat as clinically indicated.

    5.16 Infection

    Serious infections (with or without neutropenia), including some with fatal outcome, have been reported. Monitor patients for signs and symptoms of infection. Institute appropriate anti-infective therapy promptly and consider interruption or discontinuation of pazopanib for serious infections.

    5.17 Increased Toxicity with Other Cancer Therapy

    Pazopanib is not indicated for use in combination with other agents. Clinical trials of pazopanib in combination with pemetrexed and lapatinib were terminated early due to increased toxicity and mortality. The fatal toxicities observed included pulmonary hemorrhage, gastrointestinal hemorrhage, and sudden death. A safe and effective combination dose has not been established with these regimens.

    5.18 Increased Toxicity in Developing Organs

    The safety and effectiveness of pazopanib in pediatric patients have not been established. Pazopanib is not indicated for use in pediatric patients. Based on its mechanism of action, pazopanib may have severe effects on organ growth and maturation in patients younger than 2 years of age [see  Use in Specific Populations (8.4)] .

    5.19 Embryo-Fetal Toxicity

    Based on findings from animal studies and its mechanism of action, pazopanib can cause fetal harm when administered to a pregnant woman. Administration of pazopanib to pregnant rats and rabbits during the period of organogenesis resulted in maternal toxicity, teratogenicity, and abortion at systemic exposures lower than that observed at the maximum recommended human dose (MRHD) of 800 mg (based on area under the curve [AUC]).

    Advise pregnant women of the potential risk to a fetus. Advise females of reproductive potential to use effective contraception during treatment with pazopanib and for at least 2 weeks following the final dose. Advise males (including those who have had vasectomies) with female partners of reproductive potential to use condoms during treatment with pazopanib and for at least 2 weeks after the last dose [see Use in Specific Populations (8.1, 8.3)] .

  • 6 ADVERSE REACTIONS

    The following clinically significant adverse reactions are elsewhere in the labeling:

    6.1 Clinical Trials Experience

    Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared with rates in the clinical trials of another drug and may not reflect the rates observed in practice.

    The data described in the WARNINGS AND PRECAUTIONS section reflect exposure of 977 patients who received pazopanib as a single agent, including 586 pazopanib-treated patients with RCC. With a median duration of treatment of 7.4 months (range, 0.1 to 27.6) in these 977 patients, the most common adverse reactions (≥ 20%) in these 586 patients were diarrhea, hypertension, hair color change, nausea, fatigue, anorexia, and vomiting.

    The data described in the WARNINGS AND PRECAUTIONS also reflects exposure of 382 patients with advanced soft tissue sarcoma who received pazopanib as a single agent, with a median duration of treatment of 3.6 months (range, 0 to 53). The most common adverse reactions (≥ 20%) in these 382 patients were fatigue, diarrhea, nausea, decreased weight, hypertension, decreased appetite, vomiting, tumor pain, hair color changes, musculoskeletal pain, headache, dysgeusia, dyspnea, and skin hypopigmentation.

    Renal Cell Carcinoma

    The safety of pazopanib was evaluated in 290 patients with RCC who participated in VEG105192, a randomized, double-blind, placebo-controlled trial [see Clinical Studies (14.1)] . The median duration of treatment was 7.4 months (range, 0 to 23) for patients who received pazopanib.

    Forty-two percent of patients on pazopanib required a dose interruption and 36% required a dose reduction.

    Table 3 presents adverse reactions in VEG105192.

    Table 3. Adverse Reactions (≥ 10%) in Patients with RCC Who Received Pazopanib in VEG105192
    Abbreviation: RCC, renal cell carcinoma.
    aNational Cancer Institute Common Terminology Criteria for Adverse Events, version 3.
    Pazopanib
    (N = 290)     		Placebo
    (N = 145)
    All GradesaGrade 3Grade 4All GradesaGrade 3Grade 4
    Adverse reactions%%%%%%
    Diarrhea523< 19< 10
    Hypertension404010< 10
    Hair color changes38< 10300
    Nausea26< 10900
    Anorexia222010< 10
    Vomiting212< 1820
    Fatigue1920811
    Asthenia1430800
    Abdominal pain1120100
    Headache1000500

    Other adverse reactions observed more commonly in patients treated with pazopanib than placebo and that occurred in < 10% (any grade) were alopecia (8% versus < 1%), chest pain (5% versus 1%), dysgeusia (8% versus < 1%), dyspepsia (5% versus < 1%), dysphonia (4% versus < 1%), facial edema (1% versus 0%), palmar-plantar erythrodysesthesia (6% versus < 1%), proteinuria (9% versus 0%), rash (8% versus 3%), skin depigmentation (3% versus 0%), and weight decreased (9% versus 3%).

    Table 4 presents the laboratory abnormalities in VEG105192.

    Table 4. Select Laboratory Abnormalities (> 10%) in Patients with RCC Who Received Pazopanib with a Difference Between Arms of ≥ 5% Compared to Placebo in VEG105192
    Abbreviations: ALT, alanine aminotransferase; AST, aspartate aminotransferase; RCC, renal cell carcinoma.
    aNational Cancer Institute Common Terminology Criteria for Adverse Events, version 3.
    Pazopanib 
    (N = 290)     		Placebo
    (N = 145)
    All GradesaGrade 3Grade 4All GradesaGrade 3Grade 4
    Parameters%%%%%%
    Chemistry
          ALT increased531022210
          AST increased537< 119< 10
          Glucose increased41< 103310
          Total bilirubin increased363< 1101< 1
          Phosphorus decreased34401100
          Sodium decreased31412440
          Magnesium decreased 26< 111400
          Glucose decreased170< 1300
    Hematologic
          Leukopenia3700600
          Neutropenia341< 1600
          Thrombocytopenia32< 1< 150< 1
          Lymphocytopenia314< 12410

    Additional adverse reactions from other clinical trials in patients with RCC who received pazopanib include arthralgia and muscle spasms.

    Soft Tissue Sarcoma

    The safety of pazopanib was evaluated in 240 patients who participated in VEG110727, a randomized, double-blind, placebo-controlled trial [see Clinical Studies (14.2)] . The median duration of treatment was 4.5 months (range, 0 to 24) for patients who received pazopanib.

    Fifty-eight percent of patients on pazopanib required a dose interruption and 38% required a dose reduction. Seventeen percent of patients who received pazopanib discontinued therapy due to adverse reactions.

    Table 5 presents the adverse reactions in VEG110727.

    Table 5. Adverse Reactions (≥ 10%) in Patients with STS Who Received Pazopanib in VEG110727
    Abbreviation: STS, soft tissue sarcoma.
    aNational Cancer Institute Common Terminology Criteria for Adverse Events, version 3.
    b27 of the 28 cases of skin disorder were palmar-plantar erythrodysesthesia.
    Pazopanib
    (N = 240)     		Placebo
    (N = 123)
    All GradesaGrade 3Grade 4All GradesaGrade 3Grade 4
    Adverse reactions%%%%%%
    Fatigue651314841
    Diarrhea59501510
    Nausea56302220
    Weight decreased48401500
    Hypertension4270600
    Appetite decreased40601900
    Hair color changes3900200
    Vomiting33301110
    Tumor pain29802172
    Dysgeusia2800300
    Headache2310800
    Musculoskeletal pain23202020
    Myalgia2320900
    Gastrointestinal pain2330940
    Dyspnea205< 11751
    Exfoliative rash18< 10900
    Cough17< 1012< 10
    Peripheral edema1420920
    Mucositis1220200
    Alopecia1200100
    Dizziness1110400
    Skin disorder b1120100
    Skin hypopigmentation1100000
    Stomatitis11< 10300
    Chest pain1020600

    Other adverse reactions observed more commonly in patients treated with pazopanib that occurred in ≥ 5% of patients and at an incidence of more than 2% difference from placebo included insomnia (9% versus 6%), hypothyroidism (8% versus 0%), dysphonia (8% versus 2%), epistaxis (8% versus 2%), left ventricular dysfunction (8% versus 4%), dyspepsia (7% versus 2%), dry skin (6% versus < 1%), chills (5% versus 1%), vision blurred (5% versus 2%), and nail disorder (5% versus 0%).

    Table 6 presents the laboratory abnormalities in VEG110727.

    Table 6. Select Laboratory Abnormalities (> 10%) in Patients with STS Who Received Pazopanib with a Difference Between Arms of ≥ 5% Compared to Placebo in VEG110727
    Abbreviations: ALT, alanine aminotransferase; AST, aspartate aminotransferase; STS, soft tissue sarcoma.
    aNational Cancer Institute Common Terminology Criteria for Adverse Events, version 3.
    Pazopanib 
    (N = 240)     		Placebo
    (N = 123)
    All GradesaGrade 3Grade 4All GradesaGrade 3Grade 4
    Parameters%%%%%%
    Chemistry
          AST increased51532220
          ALT increased46821821
          Glucose increased45< 103520
          Albumin decreased34102100
          Alkaline phosphatase increased32302310
          Sodium decreased31402030
          Total bilirubin increased2910720
          Potassium increased16101100
    Hematologic
          Leukopenia44101500
          Lymphocytopenia431003692
          Thrombocytopenia3631600
          Neutropenia3340700

    Other Clinically Relevant Adverse Reactions

    Lipase Elevations

    In a single-arm RCC trial (VEG102616), elevated lipase was observed for 27% of 181 patients with available laboratory data. Elevated lipase as an adverse reaction was reported for 4% of 225 patients, including 2.7% (6/225) with Grade 3 and 0.4% (1/225) with Grade 4. In the RCC trials, clinical pancreatitis was observed in < 1% of 586 patients.

    Pneumothorax

    Two of 290 patients (0.7%) treated with pazopanib in the randomized RCC trial (VEG105192) and 8 of 240 patients (3.3%) treated with pazopanib in the randomized STS trial (VEG110727) developed a pneumothorax.

    Bradycardia

    In the randomized RCC trial (VEG105192), bradycardia based on vital signs (< 60 beats per minute) was observed in 19% of 280 patients treated with pazopanib. Bradycardia was reported as an adverse reaction in 2% of 290 patients.

    In the randomized STS trial (VEG110727), bradycardia based on vital signs (< 60 beats per minute) was observed in 19% of 238 patients treated with pazopanib. Bradycardia was reported as an adverse reaction in 2% of 240 patients.

    Adverse Reactions in East Asian Patients

    In an analysis of pooled clinical trial data (N = 1,938) with pazopanib, Grade 3 and Grade 4 neutropenia (12% versus 2%), thrombocytopenia (6% versus < 1%) and palmar-plantar erythrodysesthesia (6% versus 2%) were observed more frequently in patients of East Asian descent than in patients of non-East Asian descent.

    6.2 Postmarketing Experience

    The following adverse reactions have been identified during post‑approval use of pazopanib. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate the frequency or establish a causal relationship to drug exposure.

    Blood and Lymphatic System Disorders: Polycythemia

    Eye Disorders:Retinal detachment/tear

    Gastrointestinal Disorders:Pancreatitis

    Metabolic and Nutrition Disorder:Tumor lysis syndrome (including fatal cases)

    Vascular Disorders:Arterial (including aortic) aneurysms, dissections, and rupture (including fatal cases)

  • 7 DRUG INTERACTIONS

    7.1 Effect of Other Drugs on Pazopanib

    Strong CYP3A4 Inhibitors

    Co-administration of pazopanib with strong inhibitors of CYP3A4 increases pazopanib concentrations [see Clinical Pharmacology (12.3)] . Avoid co-administration of pazopanib with strong CYP3A4 inhibitors and consider an alternate concomitant medication with no or minimal enzyme inhibition potential. If co‑administration of a strong CYP3A4 inhibitor cannot be avoided, reduce the dose of pazopanib [see  Dosage and Administration (2.4)] .

    Strong CYP3A4 Inducers

    Co-administration of strong CYP3A4 inducers may decrease plasma pazopanib concentrations. Consider an alternate concomitant medication with no or minimal enzyme induction potential. Pazopanib is not recommended if chronic use of strong CYP3A4 inducers cannot be avoided [see Dosage and Administration(2.4)] .

    Transporters

    Co-administration of strong inhibitors of P-gp or BCRP may increase pazopanib concentrations. Avoid concomitant use of pazopanib with strong inhibitors of P-gp or BCRP. Consider selection of alternative concomitant medicinal products with no or minimal potential to inhibit P-gp or BCRP.

    7.2 Effects of Pazopanib on Other Drugs

    CYP Substrates

    Co-administration of pazopanib with agents with narrow therapeutic windows that are metabolized by CYP3A4, CYP2D6, or CYP2C8 may result in inhibition of the metabolism of these products and create the potential for serious adverse reactions. The concomitant use of pazopanib with agents with narrow therapeutic windows that are metabolized by CYP3A4, CYP2D6, or CYP2C8 is not recommended [see  ClinicalPharmacology (12.3)] .

    7.3 Concomitant Use with Simvastatin

    Concomitant use of pazopanib with simvastatin increases the incidence of ALT elevations. Across clinical trials of pazopanib as a single agent, ALT > 3 × ULN was reported in 126/895 (14%) of patients who did not use statins compared with 11/41 (27%) of patients who had concomitant use of simvastatin. If a patient receiving concomitant simvastatin develops ALT elevations, increase to weekly monitoring of liver function as recommended. Withhold pazopanib and resume at reduced dose, or permanently discontinue based on severity of hepatotoxicity [see Dosage and Administration (2.2), Warnings and Precautions (5.1)] . Insufficient data are available to assess the risk of concomitant administration of alternative statins and pazopanib.

    7.4 Concomitant Use with Gastric Acid-Reducing Agents

    Concomitant use of pazopanib with esomeprazole, a PPI, decreased the exposure of pazopanib. Avoid concomitant use of pazopanib with gastric acid-reducing agents. If concomitant administration with a gastric acid-reducing agent cannot be avoided, consider short-acting antacids in place of PPIs and H2-receptor antagonists. Separate short‑acting antacid and pazopanib dosing by several hours to avoid a reduction in pazopanib exposure [see Dosage and Administration (2.4), Clinical Pharmacology (12.3)] .

    7.5 Drugs That Prolong the QT Interval

    Pazopanib is associated with QTc interval prolongation [see Warnings and Precautions (5.2), Clinical Pharmacology (12.2)] . Avoid co-administration of pazopanib with drugs known to prolong the QT/QTc interval.

  • 8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    Risk Summary

    Based on animal reproduction studies and its mechanism of action [see Clinical Pharmacology (12.1)] , pazopanib can cause fetal harm when administered to a pregnant woman. There are no available data on pazopanib use in pregnant women to evaluate for a drug-associated risk. In animal developmental and reproductive toxicology studies, oral administration of pazopanib to pregnant rats and rabbits throughout organogenesis resulted in teratogenicity, and abortion at systemic exposures lower than that observed at the MRHD of 800 mg/day (based on AUC) ( see Data). Advise pregnant women of the potential risk to a fetus.

    The estimated background risk of major birth defects and miscarriage for the indicated population is unknown. All pregnancies have a background risk of birth defect, loss or other adverse outcomes. In the U.S. general population, the estimated background risk of major birth defects in clinically recognized pregnancies and miscarriage is 2% to 4% and 15% to 20%, respectively.

    Data

    Animal Data

    In a female fertility and early embryonic development study, female rats were administered oral pazopanib at least 15 days prior to mating and for 6 days after mating, which resulted in increased pre-implantation loss and early resorptions at dosages greater than or equal to 30 mg/kg/day (approximately 0.4-fold the AUC at the MRHD of 800 mg/day). Total litter resorption was seen at 300 mg/kg/day (approximately 0.8-fold the AUC at the MRHD of 800 mg/day). Postimplantation loss, embryolethality, and decreased fetal body weights were noted in females administered doses greater than or equal to 10 mg/kg/day (approximately 0.3-fold the AUC at the MRHD of 800 mg/day).

    In embryo-fetal developmental toxicity studies in rats and rabbits, oral pazopanib was administered to pregnant animals during organogenesis. In rats, dose levels of greater than or equal to 3 mg/kg/day (approximately 0.1-fold the AUC at the MRHD of 800 mg/day) resulted in teratogenic effects, including cardiovascular malformations (retroesophageal subclavian artery, missing innominate artery, changes in the aortic arch), incomplete or absent ossification, increases in postimplantation loss, embryolethality and reduced fetal body weight. In rabbits, maternal toxicity, increased postimplantation loss and abortion were observed at doses greater than or equal to 30 mg/kg/day (approximately 0.007-fold the AUC at the MRHD of 800 mg/day). In addition, severe maternal body weight loss and 100% litter loss were observed at doses greater than or equal to 100 mg/kg/day (0.02-fold the AUC at the MRHD of 800 mg/day), while fetal weight was reduced at doses greater than or equal to 3 mg/kg/day (AUC not calculated).

    8.2 Lactation

    Risk Summary

    There is no data on the presence of pazopanib or its metabolites in human milk or their effects on the breastfed infant or milk production. Because of the potential for serious adverse reactions in breastfed infants, advise women not to breastfeed during treatment with pazopanib and for 2 weeks after the final dose.

    8.3 Females and Males of Reproductive Potential

    Pazopanib can cause fetal harm when administered to a pregnant woman [see Use in Specific Populations (8.1)] .

    Pregnancy Testing

    Verify pregnancy status of females of reproductive potential prior to starting treatment with pazopanib.

    Contraception

    Females

    Advise females of reproductive potential to use effective contraception during treatment with pazopanib and for at least 2 weeks after the last dose.

    Males

    Advise males (including those who have had vasectomies) with female partners of reproductive potential to use condoms during treatment with pazopanib and for at least 2 weeks after the last dose.

    Infertility

    Based on findings from animal studies, pazopanib may impair fertility in females and males of reproductive potential while receiving treatment [see Nonclinical Toxicology (13.1)].

    8.4 Pediatric Use

    The safety and effectiveness of pazopanib in pediatric patients have not been established.

    Pazopanib is not indicated for use in pediatric patients [seeWarnings and Precautions (5.18)]. Based on its mechanism of action, pazopanib may have severe effects on organ growth and maturation during early postnatal development. Administration of pazopanib to juvenile rats < 21 days old resulted in toxicity to the lungs, liver, heart, and kidney and in death at doses significantly lower than the clinically recommended dose or doses tolerated in older animals (see Juvenile Animal Toxicity Data). 

    The safety and efficacy of pazopanib or an unapproved pazopanib formulation were investigated but not established in two open-label studies: a study in 37 pediatric patients 2 years to < 17 years with recurrent or refractory solid tumors [ NCT00929903] and a study in 46 pediatric patients 1 year to < 17 years with refractory solid tumors, including sarcoma [ NCT01956669]. Meaningful anti-tumor activity was not observed in these studies.] and a study in 46 pediatric patients 1 year to < 17 years with refractory solid tumors, including sarcoma [NCT01956669]. Meaningful anti-tumor activity was not observed in these studies.

    Juvenile Animal Toxicity Data

    In rats, weaning occurs at Day 21 postpartum which approximately equates to a human pediatric age of 2 years. In a juvenile animal toxicology study performed in rats, when animals were dosed from Day 9 through Day 14 postpartum (pre-weaning), pazopanib caused abnormal organ growth/maturation in the kidney, lung, liver, and heart at approximately 0.1-fold the AUC in adults at the MRHD of 800 mg/day of pazopanib. At approximately 0.4-fold the AUC in adults at the MRHD of 800 mg/day, pazopanib administration resulted in mortality.

    In repeat-dose toxicology studies in rats, including 4-week, 13-week, and 26-week administration, toxicities in bone, teeth, and nail beds were observed at doses greater than or equal to 3 mg/kg/day (approximately 0.07-fold the AUC at the MRHD of 800 mg/day). Doses of 300 mg/kg/day (approximately 0.8-fold the AUC at the MRHD of 800 mg/day) were not tolerated in 13-week and 26-week studies and animals required dose reductions due to body weight loss and morbidity. Hypertrophy of epiphyseal growth plates, nail abnormalities (including broken, overgrown, or absent nails) and tooth abnormalities in growing incisor teeth (including excessively long, brittle, broken, and missing teeth, and dentine and enamel degeneration and thinning) were observed in rats at doses greater than or equal to 30 mg/kg/day (approximately 0.35-fold the AUC at the MRHD of 800 mg/day) at 26 weeks, with the onset of tooth and nail bed alterations noted clinically after 4 weeks to 6 weeks. Similar findings were noted in repeat-dose studies in juvenile rats dosed with pazopanib beginning Day 21 postpartum (post‑weaning). In the post-weaning animals, the occurrence of changes in teeth and bones occurred earlier and with greater severity than in older animals. There was evidence of tooth degeneration and decreased bone growth at doses greater than or equal to 30 mg/kg (approximately 0.1‑fold to 0.2-fold the AUC at the MRHD of 800 mg/day). Pazopanib exposure in juvenile rats was lower than that seen at the same dose levels in adult animals, based on comparative AUC values. At pazopanib doses approximately 0.5-fold to 0.7-fold the AUC at the MRHD of 800 mg/day, decreased bone growth in juvenile rats persisted even after the end of the dosing period. Finally, despite lower pazopanib exposures than those reported in adult animals or adult humans, juvenile animals administered 300 mg/kg/dose pazopanib required dose reduction within 4 weeks of dosing initiation due to significant toxicity, although adult animals could tolerate this same dose for at least 3 times as long [see Warnings and Precautions (5.18)].

    8.5 Geriatric Use

    In pooled clinical trials with pazopanib, 30% of 2,080 patients were aged ≥ 65 years. More patients ≥ 65 years had ALT elevations > 3 × ULN compared to patients < 65 years (23% versus 18%) [see Warnings andPrecautions (5.1)].

    In the RCC trials, 33% of 586 patients were aged ≥ 65 years. No overall differences in safety or effectiveness of pazopanib were observed between these patients and younger patients. 

    In the STS trials, 24% of 382 patients were aged ≥ 65 years. Patients aged ≥ 65 years had a higher incidence of Grade 3 or Grade 4 fatigue (19% versus 12% for patients aged < 65 years), hypertension (10% versus 6%), decreased appetite (11% versus 2%), ALT elevations (3% versus 2%) and AST elevations (4% versus 1%). In the randomized STS trial (VEG110727), no overall differences in effectiveness of pazopanib were observed between patients aged ≥ 65 years and younger patients.

    8.6 Renal Impairment

    No dose adjustment is recommended for patients with renal impairment. Pazopanib has not been studied in patients with severe renal impairment or in patients undergoing peritoneal dialysis or hemodialysis.

    8.7 Hepatic Impairment

    No dose adjustment is required in patients with mild hepatic impairment (either total bilirubin ≤ ULN and ALT > ULN or bilirubin > 1 to 1.5 × ULN and any ALT value). Pazopanib is not recommended in patients with moderate (total bilirubin > 1.5 to 3 × ULN and any ALT value) and severe (total bilirubin > 3 × ULN and any ALT value) hepatic impairment [see Dosage and Administration (2.3), Clinical Pharmacology (12.3)] .

  • 10 OVERDOSAGE

    Dose-limiting toxicity (Grade 3 fatigue) and Grade 3 hypertension were each observed in 1 of 3 patients dosed at 2,000 mg daily (2.5 times the recommended dose) and 1,000 mg daily (1.25 times the recommended dose), respectively.

    Provide general supportive measures to manage an overdose. Hemodialysis is not expected to enhance the elimination of pazopanib because pazopanib is not significantly renally excreted and is highly bound to plasma proteins.

  • 11 DESCRIPTION

    Pazopanib is a kinase inhibitor. Pazopanib is presented as the hydrochloride salt, with the chemical name 5-[[4-[(2,3-Dimethyl-2H-indazol-6-yl)methylamino]-2-pyrimidinyl]amino]-2-methylbenzolsulfonamide hydrochloride. It has the molecular formula C 21H 23N 7O 2SHCl and a molecular weight of 473.99 g/mol.

    Pazopanib hydrochloride has the following chemical structure:

    chemical structure

    Pazopanib hydrochloride is a white to off-white powder. It is sparingly soluble in dimethyl sulfoxide, slightly soluble in methanol, practically insoluble in acetonitrile, and in water.

    Pazopanib tablets are for oral use. Each tablet contains 200 mg of pazopanib free base equivalent to 216.7 mg of pazopanib hydrochloride. The inactive ingredients of pazopanib tablets are: Tablet Core:magnesium stearate, microcrystalline cellulose, povidone, and sodium starch glycolate. Coating:Gray film-coat: hypromellose, iron oxide black, iron oxide yellow, macrogol/polyethylene glycol 400 (PEG 400), polysorbate 80, and titanium dioxide.

  • 12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    Pazopanib is a multi-tyrosine kinase inhibitor of vascular endothelial growth factor receptor (VEGFR)-1, VEGFR-2, VEGFR-3, platelet‑derived growth factor receptor (PDGFR)-α and PDGFR-β, fibroblast growth factor receptor (FGFR)-1 and FGFR-3, cytokine receptor (Kit), interleukin-2 receptor-inducible T-cell kinase (Itk), lymphocyte-specific protein tyrosine kinase (Lck), and transmembrane glycoprotein receptor tyrosine kinase (c-Fms). In vitro, pazopanib inhibited ligand-induced autophosphorylation of VEGFR-2, Kit, and PDGFR-β receptors. In vivo, pazopanib inhibited VEGF-induced VEGFR-2 phosphorylation in mouse lungs, angiogenesis in a mouse model, and the growth of some human tumor xenografts in mice.

    12.2 Pharmacodynamics

    Increases in blood pressure have been observed and are related to steady-state trough plasma pazopanib concentrations.

    Cardiac Electrophysiology

    The QT prolongation potential of pazopanib was assessed in a randomized, blinded, parallel trial (N = 96) using moxifloxacin as a positive control. Pazopanib 800 mg orally under fasting conditions was administered on Days 2 to 8 and 1,600 mg was administered on Day 9 after a meal in order to increase exposure to pazopanib and its metabolites. No large changes (i.e., > 20 msec) in QTc interval following exposure to pazopanib were detected in this QT trial. The trial was not able to exclude small changes (< 10 msec) in QTc interval, because assay sensitivity below this threshold (< 10 msec) was not established in this trial [see Warnings and Precautions (5.2)] .

    12.3 Pharmacokinetics

    The recommended dosage of 800 mg once daily results in mean AUC of 1,037 mcgh/mL and C maxof 58.1 mcg/mL. There was no consistent increase in AUC or C maxat pazopanib doses above 800 mg.

    Administration of a single 400-mg crushed tablet increased AUC 0-72hby 46% and C maxby approximately 2-fold and decreased T maxby approximately 2 hours compared with administration of the whole tablet [see Dosage and Administration (2.1)] .

    Absorption

    The median time to achieve peak concentrations was 2 hours to 4 hours after a dose.

    Effect of Food

    Systemic exposure to pazopanib is increased when administered with food. Administration of pazopanib with a high-fat (approximately 50% fat) or low-fat (approximately 5% fat) meal results in an approximately 2-fold increase in AUC and C max.

    Distribution

    Binding of pazopanib to human plasma protein in vivowas > 99% with no concentration dependence over the range of 10 mcg/mL to 100 mcg/mL. In vitrostudies suggest that pazopanib is a substrate for P-gp and BCRP.

    Elimination

    Pazopanib has a mean half-life of 31 hours after administration of the recommended dose of 800 mg.

    Metabolism

    In vitrostudies demonstrated that pazopanib is metabolized by CYP3A4 with a minor contribution from CYP1A2 and CYP2C8.

    Excretion

    Elimination is primarily via feces with renal elimination accounting for < 4% of the administered dose.

    Specific Populations

    Patients with Hepatic Impairment

    Table 7 presents a comparison of the median steady-state C maxand the median AUC 0-24hvalues for patients with normal, mild, moderate and severe hepatic impairment.

    The median steady-state of pazopanib C maxand AUC 0-24hafter a once-daily dose of 800 mg in patients with mild impairment were in a similar range as the median steady-state C maxand median AUC 0-24hin patients with no hepatic impairment.

    The maximum tolerated pazopanib dose in patients with moderate hepatic impairment was 200 mg once daily. The median steady-state C maxand the median AUC 0-24hwere approximately 43% and 29%, respectively, of the corresponding median values after administration of 800 mg once daily in patients with no hepatic impairment.

    The median steady-state C maxand the median AUC 0-24hwere approximately 18% and 15%, respectively, of the corresponding median values after administration of 800 mg once daily in patients with no hepatic impairment.

    Table 7. Pharmacokinetic Parameters of Pazopanib in Patients with Hepatic Impairment
    Abbreviations: ALT, alanine aminotransferase; AUC, area under the curve; C max, maximum concentration; ULN, upper limit of normal.
    No hepatic impairmentMild hepatic impairment
    (total bilirubin ≤ ULN and ALT > ULN
    or
    total bilirubin > 1 to 1.5 × ULN and any ALT value)     		Moderate hepatic impairment
    (total bilirubin > 1.5 to 3 × ULN and any ALT value)     		Severe hepatic impairment
    (total bilirubin > 3 × ULN and any ALT value)
    Dose800 mg once daily800 mg once daily200 mg once daily200 mg once daily
    Median steady-state C max(range) mcg/mL 52
    (17 to 86)     		34
    (11 to 104)     		22
    (4.2 to 33)     		9.4
    (2.4 to 24)
    Median AUC 0-24h(range) mcgh/mL 888
    (346 to 1,482)     		774
    (215 to 2,034)     		257
    (66 to 488)     		131
    (47 to 473)

    Drug Interactions Studies

    Clinical Studies

    Strong CYP3A4 Inhibitor:Co-administration of multiple doses of oral pazopanib 400 mg with multiple doses of oral ketoconazole 400 mg (strong CYP3A4/P-gp inhibitor) resulted in a 1.7-fold increase in the AUC 0-24hand a 1.5-fold increase in the C maxof pazopanib [see Dosage and Administration (2.4), Drug Interactions (7.1)] .

    Weak CYP3A4 Inhibitor:Co-administration of 1,500 mg lapatinib, a substrate and weak inhibitor of CYP3A4, P-gp, and BCRP, with pazopanib 800 mg resulted in an approximately 50% to 60% increase in mean pazopanib AUC 0-24hand C max.

    CYP1A2, CYP2C9 and CYP2C19 Substrates:Clinical studies, using pazopanib 800 mg once daily, have demonstrated that pazopanib does not have a clinically relevant effect on the pharmacokinetics of caffeine (CYP1A2 probe substrate), warfarin (CYP2C9 probe substrate), or omeprazole (CYP2C19 probe substrate) in patients with cancer.

    CYP3A4, CYP2D6, and CYP2C8 Substrates:Co-administration of pazopanib resulted in an increase of approximately 30% in the mean AUC and C maxof midazolam (CYP3A4 probe substrate) and increases of 33% to 64% in the ratio of dextromethorphan to dextrorphan concentrations in the urine after oral administration of dextromethorphan (CYP2D6 probe substrate). Co-administration of pazopanib 800 mg once daily and paclitaxel 80 mg/m 2(CYP3A4 and CYP2C8 substrate) once weekly resulted in a mean increase of 26% and 31% in paclitaxel AUC and C max, respectively [see Drug Interactions (7.2)] .

    Gastric Acid-Reducing Agents:​Co-administration of pazopanib with esomeprazole, a PPI, decreased the exposure of pazopanib by approximately 40% (AUC and C max) [see Dosage and Administration (2.4), Drug Interactions (7.4)] .

    In Vitro Studies

    In vitrostudies with human liver microsomes showed that pazopanib inhibited the activities of CYP enzymes 1A2, 3A4, 2B6, 2C8, 2C9, 2C19, 2D6, and 2E1. Potential induction of human CYP3A4 was demonstrated in an in vitrohuman pregnane X receptor (PXR) assay.

    In vitrostudies also showed that pazopanib inhibits UGT1A1 and organic anion-transporting polypeptide (OATP1B1) with IC 50s of 1.2 µM and 0.79 µM, respectively.

    12.5 Pharmacogenomics

    Pazopanib can increase serum total bilirubin levels [see Warnings and Precautions (5.1)] . In vitro studies showed that pazopanib inhibits UGT1A1, which glucuronidates bilirubin for elimination. A pooled pharmacogenetic analysis of 236 white patients who received pazopanib showed that the (TA)7/(TA)7 genotype (UGT1A1*28/*28) (underlying genetic susceptibility to Gilbert’s syndrome) was associated with a statistically significant increase in the incidence of hyperbilirubinemia relative to the (TA)6/(TA)6 and (TA)6/(TA)7 genotypes.

    In a pooled pharmacogenetic analysis of data from 31 clinical studies of pazopanib administered as either monotherapy or in combination with other agents, ALT > 3 × ULN (Grade 2) occurred in 32% (42/133) of HLA-B*57:01 allele carriers and in 19% (397/2,101) of non-carriers and ALT > 5 × ULN (Grade 3) occurred in 19% (25/133) of HLA-B*57:01 allele carriers and in 10% (213/2,101) of non-carriers. In this dataset, 6% (133/2,234) of the patients carried the HLA-B*57:01 allele [see  Warnings and Precautions (5.1)] .

  • 13 NONCLINICAL TOXICOLOGY

    13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

    The carcinogenic potential of pazopanib was evaluated in CD-1 mice, and Sprague-Dawley rats. Administration of pazopanib to mice for 2 years did not result in increased incidence of neoplasms at doses up to 100 mg/kg/day (approximately 1.4-fold the AUC at the MRHD of 800 mg/day). Administration of pazopanib to rats for 2 years resulted in findings of duodenal adenocarcinoma in males at 30 mg/kg/day (approximately 0.3-fold the AUC at the MRHD of 800 mg/day) and in females at greater than or equal to 10 mg/kg/day (approximately 0.3‑fold the AUC at the MRHD of 800 mg/day). The human relevance of these neoplastic findings is unclear.

    Pazopanib did not induce mutations in the microbial mutagenesis (Ames) assay and was not clastogenic in both the in vitrocytogenetic assay using primary human lymphocytes and in the in vivorat micronucleus assay.

    In an oral female fertility and early embryonic development study, female rats were administered pazopanib at least 15 days prior to mating, and for 6 days after mating. Pazopanib did affect fertility in female rats. Reduced fertility, including increased pre-implantation loss and early resorptions, were noted at dosages greater than or equal to 30 mg/kg/day (approximately 0.4-fold the AUC at the MRHD of 800 mg/day). Decreased corpora lutea and increased cysts were noted in mice given greater than or equal to 100 mg/kg/day for 13 weeks and ovarian atrophy was noted in rats given greater than or equal to 300 mg/kg/day for 26 weeks (approximately 1.3-fold and 0.85-fold the AUC at the MRHD of 800 mg/day). Decreased corpora lutea was also noted in monkeys given 500 mg/kg/day for up to 34 weeks (approximately 0.4-fold the AUC at the MRHD of 800 mg/day).

    Pazopanib did not affect mating or fertility in male rats. However, there were reductions in sperm production rates and testicular sperm concentrations at doses greater than or equal to 3 mg/kg/day, epididymal sperm concentrations at doses greater than or equal to 30 mg/kg/day, and sperm motility at greater than or equal to 100 mg/kg/day following 15 weeks of dosing. Following 15 weeks and 26 weeks of dosing, there were decreased testicular and epididymal weights at doses of greater than or equal to 30 mg/kg/day (approximately 0.35-fold the AUC at the MRHD of 800 mg/day); atrophy and degeneration of the testes with aspermia, hypospermia, and cribiform change in the epididymis was also observed at this dose in the 6‑month toxicity studies in male rats.

  • 14 CLINICAL STUDIES

    14.1 Renal Cell Carcinoma

    The efficacy of pazopanib was evaluated in VEG105192, a randomized, double-blind, placebo-controlled, multicenter trial ( NCT00387764). Patients with locally advanced and/or metastatic RCC who had received either no prior therapy or one prior cytokine-based systemic therapy were randomized (2:1) to receive pazopanib 800 mg once daily or placebo once daily. Eligible subjects were stratified according to the following 3 stratification factors: baseline ECOG performance status 0 versus 1; prior nephrectomy yes versus no; and prior systemic therapy for advanced RCC: treatment-naïve versus one prior cytokine-based therapy. The major efficacy outcome measure was progression-free survival (PFS). Additional outcome measures were overall survival (OS), overall response rate (ORR), and duration of response.

    Of the total of 435 patients enrolled in this trial, 233 patients had no prior systemic therapy (treatment-naïve subgroup) and 202 patients received one prior IL-2 or INFα-based therapy (cytokine-pretreated subgroup). The baseline demographic and disease characteristics were balanced between the arms receiving pazopanib and placebo. The majority of patients were male (71%) with a median age of 59 years. Eighty-six percent of patients were white, 14% were Asian, and < 1% were other. Forty-two percent were ECOG performance status 0 and 58% were ECOG performance status 1. All patients had clear cell histology (90%) or predominantly clear cell histology (10%). Approximately 50% of all patients had 3 or more organs involved with metastatic disease. The most common metastatic sites at baseline were lung (74%), lymph nodes (56%), bone (27%), and liver (25%).

    A similar proportion of patients in each arm were treatment-naïve and cytokine-pretreated (see Table 8). In the cytokine-pretreated subgroup, the majority (75%) had received interferon-based treatment. Similar proportions of patients in each arm had prior nephrectomy (89% and 88% for pazopanib and placebo, respectively).

    The analysis of the primary endpoint PFS was based on disease assessment by independent radiological review in the entire trial population. Efficacy results are presented in Table 8 and Figure 1.

    Table 8. Efficacy Results in RCC Patients by Independent Assessment in VEG105192
    Abbreviations: CI, confidence interval; CR, complete response; HR, hazard ratio; ITT, intent-to-treat; PFS, progression-free survival; PR, partial response; RCC, renal cell carcinoma.
    aPvalue < 0.001.
    bThere were only 5 objective responses.
    HR
    Endpoint/TrialpopulationPazopanib Placebo(95% CI)
    PFS
    Overall ITTN = 290N = 145
          Median (months)9.24.20.46 a
    (0.34, 0.62)
    Treatment-naïve subgroupN = 155 (53%)N = 78 (54%)
          Median (months)11.12.80.40
    (0.27, 0.60)
    Cytokine pre-treated subgroupN = 135 (47%)N = 67 (46%)
          Median (months)7.44.20.54
    (0.35, 0.84)
    Response rate (CR + PR)N = 290N = 145
          % (95% CI)30 (25.1, 35.6)3 (0.5, 6.4)–
    Duration of response
          Median (weeks) (95% CI)58.7 (52.1, 68.1)– b

    Figure 1. Kaplan-Meier Curve for Progression-free Survival in RCC by Independent Assessment for the Overall Population (Treatment-naïve and Cytokine Pre-treated Populations) in VEG105192

    Figure

    At the protocol-specified final analysis of OS, the median OS was 22.9 months for patients randomized to pazopanib and 20.5 months for the placebo arm [HR = 0.91 (95% CI: 0.71, 1.16)]. The median OS for the placebo arm includes 79 patients (54%) who discontinued placebo treatment because of disease progression and crossed over to treatment with pazopanib. In the placebo arm, 95 (66%) patients received at least one systemic anticancer treatment after progression compared with 88 (30%) patients randomized to pazopanib.

    14.2 Soft Tissue Sarcoma

    The efficacy of pazopanib was evaluated in VEG110727, a randomized, double-blind, placebo-controlled, multicenter trial ( NCT00753688). Patients with metastatic STS who had received prior chemotherapy, including anthracycline treatment, or were unsuited for such therapy, were randomized (2:1) to receive pazopanib 800 mg once daily or placebo. Patients with gastrointestinal stromal tumors (GIST) or adipocytic sarcoma were excluded from the trial. Randomization was stratified by the factors of WHO performance status (WHO PS) 0 or 1 at baseline and the number of lines of prior systemic therapy for advanced disease (0 or 1 versus 2+). The major efficacy outcome measure was PFS assessed by independent radiological review. Additional outcome measures were OS, ORR, and duration of response.

    The majority of patients were female (59%) with a median age of 55 years. Seventy-two percent of patients were white, 22% were Asian, and 6% were other. Forty-three percent of patients had leiomyosarcoma, 10% had synovial sarcoma, and 47% had other soft tissue sarcomas. Fifty-six percent of patients had received 2 or more lines of prior systemic therapy and 44% had received 0 lines or 1 lines of prior systemic therapy.

    Efficacy results are presented in Table 9 and Figure 2.

    Table 9. Efficacy Results in STS Patients by Independent Assessment in VEG110727
    Abbreviations: CI, confidence interval; CR, complete response; HR, hazard ratio; ITT, intent-to-treat; PFS, progression-free survival; PR, partial response; STS, soft tissue sarcoma.
    aPvalue < 0.001.
    bThere were 11 partial responses and 0 complete responses.
    HR
    Endpoint/Trial populationPazopanibPlacebo(95% CI)
    PFS
    Overall ITTN = 246N = 1230.35 a
       Median (months)4.61.6(0.26, 0.48)
    Leiomyosarcoma subgroupN = 109N = 490.37
       Median (months)4.61.9(0.23, 0.60)
    Synovial sarcoma subgroupN = 25N = 130.43
       Median (months)4.10.9(0.19, 0.98)
    ‘Other soft tissue sarcoma’ subgroupN = 112N = 610.39
       Median (months)4.61.0(0.25, 0.60)
    Response rate (CR + PR)
       % (95% CI)4 (2.3, 7.9) b0 (0.0, 3.0)–
    Duration of response
       Median (months) (95% CI)9.0 (3.9, 9.2)

    Figure 2. Kaplan-Meier Curve for Progression-free Survival in STS by Independent Assessment for the Overall Population in VEG110727

    Figure

    At the protocol-specified final analysis of OS, the median OS was 12.6 months for patients randomized to pazopanib and 10.7 months for the placebo arm [HR = 0.87 (95% CI: 0.67, 1.12)].

  • 16 HOW SUPPLIED/STORAGE AND HANDLING

    Pazopanib tablets, 200 mg are supplied as gray, modified capsule-shaped, film-coated tablets debossed with “P 200” on one side and plain on the other side and are available in:

    Store at 20°C to 25°C (68°F to 77°F), excursions permitted between 15°C and 30°C (59°F and 86°F) [See USP Controlled Room Temperature].

  • 17 PATIENT COUNSELING INFORMATION

    Advise the patient to read the FDA-approved patient labeling (Medication Guide).

    • Hepatic Toxicity: Inform patients that periodic laboratory testing will be performed. Advise patients to report signs and symptoms of liver dysfunction to their healthcare provider right away [see Warnings and Precautions (5.1)].
    • QT Prolongation and Torsades de Pointes: Inform patients that ECG monitoring may be performed. Advise patients to inform their physicians of concomitant medications [see Warnings and Precautions (5.2)].
    • Interstitial Lung Disease/Pneumonitis: Advise patients to report pulmonary signs or symptoms indicative of interstitial lung disease (ILD) or pneumonitis [see Warnings and Precautions (5.9)] .
    • Cardiac Dysfunction: Advise patients to report hypertension or signs and symptoms of congestive heart failure [see Warnings and Precautions (5.3)] .
    • Hemorrhagic Events: Advise patients to report unusual bleeding [see Warnings and Precautions (5.4)] .
    • Arterial Thromboembolic Events: Advise patients to report signs or symptoms of an arterial thrombosis [see Warnings and Precautions (5.5)] .
    • Pneumothorax and Venous Thromboembolic Events: Advise patients to report new onset of dyspnea, chest pain, or localized limb edema [see Warnings and Precautions (5.6), Adverse Reactions (6.1)] .
    • Posterior Reversible Encephalopathy Syndrome: Advise patients to inform their doctor if they have worsening of neurological function consistent with PRES (headache, seizure, lethargy, confusion, blindness, and other visual and neurologic disturbances) [see Warnings and Precautions (5.10)] .
    • Hypertension: Advise patients to monitor blood pressure early in the course of therapy and frequently thereafter and report increases of blood pressure or symptoms, such as blurred vision, confusion, severe headache, or nausea and vomiting [see Warnings and Precautions (5.11)] .
    • Gastrointestinal Perforation and Fistula: Advise patients to report signs and symptoms of a GI perforation or fistula [see Warnings and Precautions (5.8)] .
    • Risk of Impaired Wound Healing: Advise patients that pazopanib tablets may impair wound healing. Advise patients to inform their healthcare provider of any scheduled surgical procedure [see Warnings and Precautions (5.12)] .
    • Hypothyroidism and Proteinuria: Inform patients that thyroid function testing and urinalysis will be performed during treatment [see Warnings and Precautions (5.13, 5.14)] .
    • Tumor Lysis Syndrome: Advise patients to contact their healthcare provider promptly to report any signs and symptoms of TLS, such as abnormal heart rhythm, seizure, confusion, muscle cramps or spasms, or a decrease in urine output [see Warnings and Precautions (5.15)] .
    • Infection: Advise patients to promptly report any signs or symptoms of infection [see Warnings and Precautions (5.16)] .
    • Embryo-Fetal Toxicity: Advise female patients to inform their healthcare provider of a known or suspected pregnancy during treatment with pazopanib tablets. Inform female patients of the risk to a fetus and the potential loss of the pregnancy [see Warnings and Precautions (5.19), Use in Specific Populations (8.1)] .
      Advise females of reproductive potential to use effective contraception during treatment and for at least 2 weeks after the last dose of pazopanib tablets. Advise male patients with female partners of reproductive potential to use condoms during treatment with pazopanib tablets and for at least 2 weeks after the last dose [see Warnings and Precautions (5.19), Use in Specific Populations (8.3)] .
    • Lactation: Advise women not to breastfeed during treatment with pazopanib tablets and for 2 weeks after the last dose [see Use in Specific Populations (8.2)] .
    • Infertility: Advise males and females of reproductive potential that pazopanib tablets may impair fertility [see Use in Specific Populations (8.3)] .
    • Gastrointestinal Adverse Reactions: Advise patients on how to manage nausea, vomiting, and diarrhea and to notify their healthcare provider if moderate-to-severe vomiting or diarrhea occurs or if there is a decrease in oral intake [see Adverse Reactions (6.1)] .
    • Depigmentation: Advise patients that depigmentation of the hair or skin may occur during treatment with pazopanib tablets  [see Adverse Reactions (6.1)] .
    • Drug Interactions: Advise patients to inform their healthcare providers of all concomitant medications, vitamins, or dietary and herbal supplements [see Drug Interactions (7)] .
    • Dosage and Administration: Advise patients to take pazopanib tablets without food (at least 1 hour before or 2 hours after a meal) [see Dosage and Administration (2.1)] .

    Distributed by:
    Novugen Pharma (USA) LLC
    100 Overlook Center
    Princeton, NJ 08540, USA

    For India Manufacturing Site

    MADE IN INDIA

    Revised: 1/2024

    For Malaysia Manufacturing Site

    MADE IN MALAYSIA

    Revised: 4/2024

    3250000446

  • MEDICATION GUIDE

    This Medication Guide has been approved by the U.S. Food and Drug Administration.Revised: 4/2023
    MEDICATION GUIDE
    Pazopanib (paz-OH-pa-nib)
    Tablets
    What is the most important information I should know about pazopanib tablets?
    Pazopanib tablets can cause severe liver problems, including death.Your healthcare provider will do blood tests to check
    your liver before you start and while you take pazopanib tablets.
    Tell your healthcare provider right away if you get any of these signs of liver problems during treatment with pazopanib tablets:
         ○ yellowing of your skin or the whites of your eyes (jaundice)     ○ loss of appetite
         ○ dark urine     ○ pain on the right side of your stomach area (abdomen)
         ○ tiredness     ○ bruise easily
         ○ nausea or vomiting
    Your healthcare provider may need to prescribe a lower dose of pazopanib tablets for you or tell you to stop taking pazopanib tablets if you develop liver problems during treatment.
    What are pazopanib tablets?
    Pazopanib tablets are a prescription medicine used to treat adults with:
    • advanced renal cell cancer (RCC)
    • advanced soft tissue sarcoma (STS) who have received chemotherapy in the past
    It is not known if pazopanib tablets are effective in treating certain soft tissue sarcomas or certain gastrointestinal tumors.
    It is not known if pazopanib tablets are safe and effective in children under 18 years of age.
    What should I tell my healthcare provider before taking pazopanib tablets?
    Before taking pazopanib tablets, tell your healthcare provider about all of your medical conditions, including if you:
    • have or had liver problems. You may need a lower dose of pazopanib tablets, or your healthcare provider may prescribe a different medicine to treat your advanced renal cell cancer or advanced soft tissue sarcoma.
    • have high blood pressure
    • have heart problems or an irregular heartbeat, including QT prolongation
    • have a history of a stroke
    • have headaches, seizures, or vision problems
    • have coughed up blood in the last 6 months
    • had bleeding of your stomach or intestines in the last 6 months
    • have a history of a tear (perforation) in your stomach or intestine, or an abnormal connection between two parts of your gastrointestinal tract (fistula)
    • have had blood clots in a vein or in the lung
    • have thyroid problems
    • had recent surgery or are going to have surgery. You should stop taking pazopanib tablets at least 1 week before scheduled surgery because pazopanib tablets may affect healing after surgery. Do not take pazopanib tablets for at least 2 weeks following major surgery and until your wound heals adequately. Your healthcare provider should tell you when you may start taking pazopanib tablets again after surgery.
    • have problems with your kidney function
    • are pregnant or plan to become pregnant. Pazopanib tablets can harm your unborn baby. Your healthcare provider should check to see if you are pregnant before you start taking pazopanib tablets. You should not become pregnant while you are taking pazopanib tablets. You should use effective birth control during treatment with pazopanib tablets and for at least 2 weeks after your final dose of pazopanib tablets. Talk to your healthcare provider about types of birth control that may be right for you during this time.
    • are a male (including one who has had a vasectomy) with a sexual partner who is pregnant, think that they may be pregnant, or who could become pregnant (including those who use other forms of birth control). You should use condoms during sexual intercourse during treatment with pazopanib tablets and for at least 2 weeks after the last dose of pazopanib tablets.
    • are breastfeeding or plan to breastfeed. It is not known if pazopanib passes into your breast milk. Do not breastfeed during treatment with pazopanib tablets and for 2 weeks after the final dose.
    Tell your healthcare provider about all the medicines you take,including prescription and over-the-counter medicines, vitamins, and herbal supplements. Pazopanib tablets may affect the way other medicines work and other medicines may affect how pazopanib tablets work.
    Especially, tell your healthcare provider if you:
    • take medicines that can affect how your liver enzymes work, such as:
             ○ certain antibiotics (used to treat infections)         ○ certain medicines used to treat depression
             ○ certain medicines used to treat HIV-1         ○ medicines used to treat irregular heartbeats
    • take a medicine that contains simvastatin to treat high cholesterol levels
    • take medicines that reduce stomach acid (e.g., esomeprazole)
    • drink grapefruit juice
    Ask your healthcare provider if you are not sure if your medicine is one that is listed above.
    Know the medicines you take. Keep a list of them and show it to your healthcare provider and pharmacist when you get a new medicine.
    How should I take pazopanib tablets?
    • Take pazopanib tablets exactly as your healthcare provider tells you. Your healthcare provider will tell you how much pazopanib tablets to take.
    • Your healthcare provider may change your dose.
    • Take pazopanib tablets on an empty stomach, at least 1 hour before or 2 hours after food.
    • Swallow pazopanib tablets whole. Do not crush pazopanib tablets. It may increase the amount of pazopanib in your body.
    • Do not eat grapefruit or drink grapefruit juice during treatment with pazopanib tablets. Grapefruit products may increase the amount of pazopanib in your body.
    • If you miss a dose, take it as soon as you remember. Do not take it if it is close (within 12 hours) to your next dose. Just take the next dose at your regular time. Do not take more than 1 dose of pazopanib tablets at a time.
    • Your healthcare provider will test your urine, blood, and heart before you start and while you take pazopanib tablets.
    What are the possible side effects of pazopanib tablets?
    Pazopanib tablets may cause serious side effects, including:
    • See “What is the most important information I should know about pazopanib tablets?”
    • irregular or fast heartbeat or fainting
    • heart failure.This is a condition where your heart does not pump as well as it should and may cause you to have shortness of breath.
    • bleeding problems.These bleeding problems may be severe and cause death.
      Symptoms may include:unusual bleeding, bruising, or wounds that do not heal.
    • heart attack or stroke.Heart attack and stroke can happen with pazopanib tablets and may cause death.
      Symptoms may include:chest pain or pressure, pain in your arms, back, neck or jaw, shortness of breath, numbness or weakness on one side of your body, trouble talking, headache, or dizziness.
    • blood clots.Blood clots may form in a vein, especially in your legs (deep vein thrombosis or DVT). Pieces of a blood clot may travel to your lungs (pulmonary embolism). This may be life-threatening and cause death.
      Symptoms may include:new chest pain, trouble breathing or shortness of breath that starts suddenly, leg pain, and swelling of the arms and hands, or legs and feet, a cool or pale arm or leg.
    • Thrombotic microangiopathy (TMA), including thrombotic thrombocytopenia purpura (TTP) and hemolytic uremic syndrome (HUS).TMA is a condition involving blood clots that can happen while taking pazopanib tablets. TMA is accompanied by a decrease in red blood cells and cells that are involved in clotting. TMA may harm organs, such as the brain and kidneys.
    • tear in your stomach or intestinal wall (perforation) or an abnormal connection between two parts of your gastrointestinal tract (fistula).
      Symptoms may include:       pain, swelling in your stomach area, vomiting blood, and black sticky stools.
    • lung problems.Pazopanib tablets may cause lung problems that may lead to death. Tell your healthcare provider right away if you get a cough that will not go away or shortness of breath.
    • Posterior Reversible Encephalopathy Syndrome (PRES).PRES is a condition that can happen while taking pazopanib tablets that may cause death.
      Symptoms may include:headaches, seizures, lack of energy, confusion, high blood pressure, loss of speech, blindness or changes in vision, and problems thinking.
    • high blood pressure. High blood pressure can happen with pazopanib tablets, including a sudden and severe rise in blood pressure which may be life-threatening.These blood pressure increases usually happen in the first several months of treatment. Your blood pressure should be well controlled before you start taking pazopanib tablets. Your healthcare provider should begin checking your blood pressure within 1 week of you starting pazopanib tablets and often during treatment to make sure that your blood pressure is well controlled.
      Have someone call your healthcare provider or get medical help right awayfor you, if you get symptoms of a severe increase in blood pressure, including: severe chest pain, severe headache, blurred vision, confusion, nausea and vomiting, severe anxiety, shortness of breath, seizures, or you pass out (become unconscious).
    • thyroid problems.Your healthcare provider should check you for this during treatment with pazopanib tablets.
    • Tumor lysis syndrome (TLS).TLS is a condition that can happen during treatment with pazopanib tablets that may cause death. TLS is caused by a fast breakdown of cancer cells. Your healthcare provider may do a blood test to check you for TLS. Call your healthcare provider or get emergency medical help right away if you develop any of these symptoms during treatment with pazopanib tablets: irregular heartbeat, seizures, confusion, muscle cramps or spasms, or a decrease in urine output.
    • protein in your urine.Your healthcare provider will check you for this problem. If there is too much protein in your urine, your healthcare provider may tell you to stop taking pazopanib tablets.
    • serious infections.Serious infections can happen with pazopanib tablets and can cause death.
      Symptoms of an infection may include:       fever, cold symptoms, such as runny nose or sore throat that do not go away, flu symptoms, such as cough, tiredness, and body aches, pain when urinating, cuts, scrapes or wounds that are red, warm, swollen or painful.
    • collapsed lung (pneumothorax).A collapsed lung can happen with pazopanib tablets. Air may get trapped in the space between your lung and chest wall. This may cause you to have shortness of breath.
    Call your healthcare provider right away if you have any of the symptoms listed above.
    The most common side effects in people who take pazopanib tablets include:
    • diarrhea
    • change in hair color
    • nausea or vomiting
    • loss of appetite
    Other common side effects in people with advanced soft tissue sarcoma who take pazopanib tablets include:
    • feeling tired
    • decreased weight
    • tumor pain
    • muscle or bone pain
    • stomach pain
    • headache
    • taste changes
    • trouble breathing
    • change in skin color
    These are not all the possible side effects of pazopanib tablets. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
    How should I store pazopanib tablets?
    Store pazopanib tablets at room temperature between 68°F and 77°F (20°C to 25°C).
    Keep pazopanib tablets and all medicines out of the reach of children.
    General information about the safe and effective use of pazopanib tablets.
    Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. Do not use pazopanib tablets for a condition for which it was not prescribed. Do not give pazopanib tablets to other people even if they have the same symptoms that you have. It may harm them.
    You can ask your pharmacist or healthcare provider for information about pazopanib tablets that is written for healthcare professionals.

    What are the ingredients in pazopanib tablets?
    Active ingredient:pazopanib.
    Inactive ingredients: Tablet core:magnesium stearate, microcrystalline cellulose, povidone, and sodium starch glycolate. Coating: Gray film-coat: hypromellose, iron oxide black, iron oxide yellow, macrogol/polyethylene glycol 400 (PEG 400), polysorbate 80, and titanium dioxide.

    Distributed by:

    Novugen Pharma (USA) LLC
    100 Overlook Center
    Princeton, NJ 08540, USA

    For India Manufacturing Site

    MADE IN INDIA

    For Malaysia Manufacturing Site

    MADE IN MALAYSIA

    For more information, call Novugen Pharma (USA) LLC at 1-888-966-8843.

  • PRINCIPAL DISPLAY PANEL - India Manufacturing Site

    NDC: 82293-022-10

    Pazopanib Tablets

    200 mg

    PHARMACIST: Dispense the accompanying Medication Guide to each patient.

    120 Tablets

    Rx only

    Label

  • PRINCIPAL DISPLAY PANEL - Malaysia Manufacturing Site

    NDC: 82293-022-10

    Pazopanib Tablets

    200 mg

    PHARMACIST: Dispense the accompanying Medication Guide to each patient.

    120 Tablets

    Rx only

    Label

  • INGREDIENTS AND APPEARANCE
    PAZOPANIB 
    pazopanib hydrochloride tablet, film coated
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 82293-022
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PAZOPANIB HYDROCHLORIDE (UNII: 33Y9ANM545) (PAZOPANIB - UNII:7RN5DR86CK) PAZOPANIB200 mg
    Inactive Ingredients
    Ingredient NameStrength
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    POVIDONE K30 (UNII: U725QWY32X)  
    SODIUM STARCH GLYCOLATE TYPE A (UNII: H8AV0SQX4D)  
    HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)  
    HYPROMELLOSE 2910 (3 MPA.S) (UNII: 0VUT3PMY82)  
    FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorgrayScoreno score
    ShapeCAPSULESize14mm
    FlavorImprint Code P200
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 82293-022-10120 in 1 BOTTLE; Type 0: Not a Combination Product04/24/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA21823104/24/2024
    Labeler - Novugen Pharma (USA) LLC. (118312098)
    Registrant - Novugen Oncology Sdn. Bhd. (534414725)
    Establishment
    NameAddressID/FEIBusiness Operations
    Teyro Labs Private Limited854377573manufacture(82293-022)
    Establishment
    NameAddressID/FEIBusiness Operations
    Novugen Oncology Sdn. Bhd.659300907manufacture(82293-022)
    • © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.