NIKTIMVO- axatilimab-csfr injection

NIKTIMVO by

Drug Labeling and Warnings

NIKTIMVO by is a Prescription medication manufactured, distributed, or labeled by Incyte Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

  • 1 INDICATIONS AND USAGE

    NIKTIMVO is indicated for the treatment of chronic graft-versus-host disease (cGVHD) after failure of at least two prior lines of systemic therapy in adult and pediatric patients weighing at least 40 kg.

  • 2 DOSAGE AND ADMINISTRATION

    2.1 Recommended Dosage

    For patients weighing at least 40 kg, administer NIKTIMVO 0.3 mg/kg, up to a maximum dose of 35 mg, as an intravenous infusion over 30 minutes every 2 weeks until progression or unacceptable toxicity.


    2.2 Dosage Modifications for Adverse Reactions

    Monitor aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (ALP), creatine phosphokinase (CPK), amylase, and lipase prior to the start of NIKTIMVO therapy, every 2 weeks for the first month, and every 1 to 2 months thereafter until abnormalities are resolved.

    For recommended NIKTIMVO dosage modifications due to adverse reactions, see Table 1.

    Table 1: Recommended NIKTIMVO Dosage Modifications for Adverse Reactions
    AST = aspartate aminotransferase; ALT = alanine aminotransferase; ULN = upper limit of normal; ALP = alkaline phosphatase; CPK = creatine phosphokinase.
  • * Graded per National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) v5.
    		•
    Adverse Reaction Severity* Dosage Modification
    Infusion-related reactions [see Warnings and Precautions (5.1)] Grade 1 or 2 
    • Temporarily interrupt the infusion until resolution or decrease infusion rate by 50%.
    • Initiate symptomatic treatment (e.g., antihistamines and antipyretics).
    • For subsequent infusions, premedicate and resume the infusion at 50% of the prior infusion rate.
    Grade 3 or 4  Permanently discontinue NIKTIMVO. 
    Elevation of AST or ALT (on the day of dosing) [see Adverse Reactions (6.1)] Grade 3 with total bilirubin ≤ Grade 1
    		Withhold NIKTIMVO until recovery to Grade 2, then resume NIKTIMVO at 0.2 mg/kg (maximum 23 mg) every 2 weeks.
    Elevation of AST or ALT (regardless of the time of the reaction) [see Adverse Reactions (6.1)]
    		ALT or AST ≥ 3 times ULN with total bilirubin ≥ 2 times ULN and ALP < 2 times ULN
    		Withhold NIKTIMVO and investigate for drug-induced liver injury. If confirmed, permanently discontinue NIKTIMVO.
    Grade 4Permanently discontinue NIKTIMVO.
    Elevation of CPK, amylase, or lipase [see Adverse Reactions (6.1)]≥ Grade 3
    • If diagnostic evaluation results show no evidence of end-organ damage, continue NIKTIMVO without dose reduction.
    • If diagnostic evaluation results show evidence of end-organ damage, permanently discontinue NIKTIMVO.
    Symptomatic ≥ Grade 3
    		Permanently discontinue NIKTIMVO.
    Other Nonhematologic Adverse Reactions [see Adverse Reactions (6.1)]Grade 3Withhold NIKTIMVO until recovery to Grade 2:
    • If delayed by ≤ 4 weeks from the planned infusion, resume NIKTIMVO at 0.2 mg/kg (maximum 23 mg) every 2 weeks.
    • If delayed by > 4 weeks from the planned infusion, permanently discontinue NIKTIMVO.
    Grade 4
    		Permanently discontinue NIKTIMVO.

    2.3 Preparation and Administration

    Preparation

    • Use aseptic technique to prepare NIKTIMVO.
    • Visually inspect the vial for particulate matter and discoloration prior to dilution. NIKTIMVO is a slightly opalescent, pale brownish yellow solution. Discard the vial if the solution is cloudy, discolored, or contains visible particles.
    • Do not shake the vial.
    • Determine the dose [see Dosage and Administration (2.1)] and total volume of NIKTIMVO solution needed. Each 1 mL vial of NIKTIMVO contains 50 mg of axatilimab-csfr.

    Dilution

    • Withdraw the calculated volume of NIKTIMVO solution from the vial and add it into an intravenous infusion bag made of polyvinyl chloride (PVC), polyolefin, polyolefin with polyamide, or ethylene vinyl acetate (EVA) containing 0.9% Sodium Chloride Injection to achieve a final concentration between the range of 0.24 mg/mL and 0.75 mg/mL.
    • Discard vial with any unused portion.
    • Mix diluted solution by gentle inversion. Do not shake.
    • Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. The diluted solution is a clear to slightly opalescent, colorless solution that may contain trace amounts of translucent to white particles. Discard if the solution is cloudy, discolored, or contains extraneous particulate matter other than trace amounts of translucent to white particles.

    Storage of diluted NIKTIMVO solution

    • Immediately use diluted NIKTIMVO solution. If not used immediately, the diluted solution can be stored:

      - At room temperature [up to 25°C (77°F)] for no more than 4 hours from the time of preparation to the end of the infusion.

      OR

      - Refrigerated at 2°C to 8°C (36°F to 46°F) for no more than 24 hours. If refrigerated, allow the diluted solution to come to room temperature prior to administration. The diluted solution must be administered within 4 hours (including infusion time) once it is removed from the refrigerator.
    • Do not freeze or shake the diluted solution.

    Administration

    • Administer diluted NIKTIMVO solution by intravenous infusion over 30 minutes through a dedicated infusion line that includes a sterile, low-protein binding 0.2-micron in-line or add-on polyethersulfone (PES) filter.
    • Do not co‑administer other drugs through the same infusion line.
    • After administration, flush the infusion line with 0.9% Sodium Chloride Injection.
  • 3 DOSAGE FORMS AND STRENGTHS

    Injection: 50 mg/mL slightly opalescent, pale brownish yellow solution in a single-dose vial.

  • 4 CONTRAINDICATIONS

    None.

  • 5 WARNINGS AND PRECAUTIONS

    5.1 Infusion-Related Reactions

    NIKTIMVO can cause infusion-related reactions. Infusion-related reactions, including hypersensitivity reactions, occurred in 18% of patients who received NIKTIMVO in the clinical trial (AGAVE-201), with Grade 3 or 4 reactions in 1.3% [see Adverse Reactions (6.1)].

    Premedicate with an antihistamine and an antipyretic for patients who have previously experienced an infusion-related reaction to NIKTIMVO [see Dosage and Administration (2.2)]. Monitor patients for signs and symptoms of infusion-related reactions, including fever, chills, rash, flushing, dyspnea, and hypertension. Interrupt or slow the rate of infusion or permanently discontinue NIKTIMVO based on severity of the reaction [see Dosage and Administration (2.2)].

    5.2 Embryo-Fetal Toxicity

    Based on its mechanism of action, NIKTIMVO may cause fetal harm when administered to a pregnant woman. Advise pregnant women of the potential risk to the fetus. Advise females of reproductive potential to use effective contraception during treatment with NIKTIMVO and for 30 days after the last dose [see Use in Specific Populations (8.1, 8.3)].

  • 6 ADVERSE REACTIONS

    The following adverse reactions are described elsewhere in the labeling.

    • Infusion-Related Reactions [see Warnings and Precautions (5.1)]

    6.1 Clinical Trial 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 to rates in the clinical trials of another drug and may not reflect the rates observed in practice.

    Chronic Graft-Versus-Host Disease

    The safety of NIKTIMVO was evaluated in 79 adult and pediatric patients with cGVHD treated with NIKTIMVO 0.3 mg/kg intravenously every 2 weeks in the AGAVE‑201 trial [see Clinical Studies (14)]. The median duration of treatment was 10.3 months (range: 0.5 to 28.6 months), and 73.4% were treated for more than 6 months.

    Serious adverse reactions occurred in 44% of patients who received NIKTIMVO. Serious adverse reactions in more than 2 patients included infection (pathogen unspecified), viral infection, and respiratory failure. Permanent discontinuation of NIKTIMVO due to an adverse reaction occurred in 10% of patients and dose reduction due to adverse reaction occurred in 8% of patients. Dose interruptions due to an adverse reaction occurred in 44% of patients. The adverse reactions leading to dose interruption in more than 2 patients were viral infection, infection (pathogen unspecified), bacterial infection, musculoskeletal pain, and pyrexia.

    The most common (≥ 15%) adverse reactions, including laboratory abnormalities, were increased AST, infection (pathogen unspecified), increased ALT, decreased phosphate, decreased hemoglobin, viral infection, increased gamma glutamyl transferase (GGT), musculoskeletal pain, increased lipase, fatigue, increased amylase, increased calcium, increased CPK, increased ALP, nausea, headache, diarrhea, cough, bacterial infection, pyrexia, and dyspnea.

    Table 2 summarizes the nonlaboratory adverse reactions in AGAVE-201.

    Table 2: Adverse Reactions in ≥ 10% of Patients With cGVHD Who Received NIKTIMVO in AGAVE-201
    Graded according to NCI CTCAE v5.0.
  • * Includes abscess jaw, atypical pneumonia, bacteremia, bronchitis, conjunctivitis, cystitis, device-related infection, enterocolitis infectious, gastroenteritis, gastrointestinal infection, groin abscess, hordeolum, liver abscess, nasopharyngitis, otitis media, otitis media acute, pneumonia, respiratory tract infection, rhinitis, sepsis, sinusitis, tooth infection, upper respiratory tract infection, urinary tract infection, and wound infection.
  • † Includes adenoviral upper respiratory infection, BK virus infection, COVID-19, coronavirus infection, enterovirus infection, gastroenteritis astroviral, gastroenteritis viral, herpes simplex, herpes zoster, influenza, metapneumovirus bronchiolitis, metapneumovirus infection, norovirus infection, oral viral infection, parainfluenza viral bronchitis, parainfluenza virus infection, respiratory syncytial virus infection, rhinovirus infection, viral infection, and viral upper respiratory tract infection.
  • ‡ Includes bacterial diarrhea, bacterial vaginosis, campylobacter gastroenteritis, campylobacter infection, cellulitis, clostridium difficile colitis, clostridium difficile infection, enterococcal infection, erysipelas, hemophilus infection, lower respiratory tract infection bacterial, pseudomonal skin infection, staphylococcal bacteremia, staphylococcal infection, stenotrophomonas infection, streptococcal infection, and urinary tract infection enterococcal.
  • § Includes arthralgia, back pain, flank pain, musculoskeletal pain, myalgia, pain in extremity.
  • Includes asthenia, fatigue, and malaise.
  • # Includes localized edema and peripheral edema.
  • Þ Includes nausea and vomiting.
  • ß Includes colitis and diarrhea.
  • à Includes headache and migraine.
  • è Includes dizziness and dizziness postural.
  • ð Includes cough and productive cough.
  • ø Includes dyspnea and dyspnea exertional.
  • ý Includes bronchospasm, flushing, hot flush, hypersensitivity, infusion-related hypersensitivity reaction, infusion-related reaction, and urticaria.
  • £ Includes contusion, epistaxis, hematochezia, hematoma, and vaginal hemorrhage.
  • ¥ Includes dermatitis bullous, dermatitis exfoliative generalized, rash, and rash maculo-papular.
    		•
    Adverse Reaction
    		NIKTIMVO
    0.3 mg/kg intravenously every 2 weeks
    (N = 79) 
    All Grades (%) Grades 3-4 (%) 
    Infections and infestations
    Infection (pathogen unspecified)*5714
    Viral infection†
    		4315
    Bacterial infection‡
    		158
    Musculoskeletal and connective tissue disorders
    Musculoskeletal pain§
    		353
    General disorders and administration site conditions
    Fatigue
    		324
    Pyrexia
    		151
    Edema#
    		131
    Gastrointestinal disorders
    NauseaÞ
    		233
    Diarrheaß 185
    Nervous system disorders
    Headacheà
    		201
    Dizzinessè
    		110
    Respiratory, thoracic and mediastinal disorders
    Coughð
    		180
    Dyspneaø 153
    Immune system disorders
    Drug hypersensitivityý
    		133
    Metabolism and nutrition disorders
    Decreased appetite
    		114
    Vascular disorders
    Hemorrhage£ 111
    Skin and subcutaneous tissue disorders
    Rash¥
    		100

    Clinically relevant adverse reactions in < 10% of patients who received NIKTIMVO included:

    • Eye disorders: periorbital edema
    • Skin and subcutaneous skin disorders: pruritus
    • Vascular disorders: hypertension

    Table 3 summarizes the laboratory abnormalities in AGAVE-201.

    Table 3: Selected Laboratory Abnormalities in Patients with cGVHD Who Received NIKTIMVO in AGAVE-201
    NA = not applicable.
  • * The denominator used to calculate the rate varied from 78 to 79 based on the number of patients with at least 1 post-treatment value.
    		•
    Laboratory AbnormalityNIKTIMVO
    0.3 mg/kg intravenously every 2 weeks
    (N=79)
    All Grades*
    (%)
    		Grade 3 or 4*
    (%)
    Hematology
    Decreased hemoglobin 
    		484
    Chemistry
    Increased aspartate aminotransferase
    		615
    Increased alanine aminotransferase
    		513
    Decreased phosphate
    		51NA
    Increased gamma glutamyl transferase
    		394
    Increased lipase
    		343
    Increased amylase
    		320
    Increased calcium
    		311
    Increased alkaline phosphatase
    		280
    Increased creatine phosphokinase
    		250

     Immunogenicity: Anti-Drug Antibody–Associated Adverse Reactions

     In 276 patients with cGVHD who received NIKTIMVO in clinical trials, among the patients who developed anti-drug antibodies (ADAs), hypersensitivity reactions occurred in 26% (13/50) of patients with neutralizing antibodies (NAb) and in 4% (2/45) of those without NAb [see Clinical Pharmacology (12.6)].

  • 8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    Risk Summary

    Based on its mechanism of action, NIKTIMVO may cause fetal harm when administered to pregnant women [see Clinical Pharmacology (12.1)]. There are no available data on the use of NIKTIMVO in pregnant women to evaluate for a drug-associated risk. No animal reproductive and developmental toxicity studies have been conducted with axatilimab-csfr.

    Targeted mutation of CSF-1R or CSF-1 in rodent models results in prenatal and perinatal death, deficits in growth, and pleiotropic impact on multiple organ systems, including skeletal and reproductive. Regulation by CSF-1R on non-mononuclear phagocytic cells and macrophages plays a role in the innate immune protection of the fetus and in pregnancy maintenance and embryo-fetal development. Human immunoglobulin G (IgG) is known to cross the placenta; therefore, NIKTIMVO has the potential to be transmitted from the mother to the developing fetus. Advise women of the potential risk to the fetus.

    In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2% to 4% and 15% to 20%, respectively.

    8.2 Lactation

    Risk Summary

    There are no data on the presence of axatilimab-csfr in human milk or the effects on the breastfed child or milk production. Maternal IgG is known to be present in human milk. Because of the potential for serious adverse reactions in a breastfed child, advise women not to breastfeed during treatment and for 30 days after the last dose of NIKTIMVO.

    8.3 Females and Males of Reproductive Potential

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

    Pregnancy Testing

    Verify pregnancy status in females of reproductive potential prior to initiating NIKTIMVO [see Use in Specific Populations (8.1)].

    Contraception

    Females

    Advise females of reproductive potential to use effective contraception during treatment with NIKTIMVO and for 30 days after the last dose of NIKTIMVO.

    8.4 Pediatric Use

    The safety and effectiveness of NIKTIMVO for the treatment of cGVHD after failure of at least two prior lines of systemic therapy have been established in pediatric patients weighing at least 40 kg. Use of NIKTIMVO in pediatric patients weighing at least 40 kg is supported by evidence from clinical trials that included 3 children (ages 6 to less than 12 years old) and 5 adolescents (ages 12 to less than 17 years old) [see Clinical Studies (14)]. The safety and effectiveness of NIKTIMVO have not been established in pediatric patients weighing less than 40 kg.

    Compared to adult and pediatric patients weighing 40 kg and above, patients weighing less than 40 kg had lower maximum concentration, trough concentration, and average concentration at the same weight-based dosage.

    Based on findings of thickening of the growth plate and metaphysis and/or degeneration of the growth plate in the femur in animals, monitor bone growth and development in pediatric patients [see Nonclinical Toxicology (13.2)].

    8.5 Geriatric Use

    Of the 79 patients with cGVHD treated with NIKTIMVO, 21 (26.6%) were 65 years and older, and 2 (2.5%) were 75 years and older [see Clinical Studies (14)]. No overall differences in the safety or effectiveness of NIKTIMVO have been observed between patients 65 years of age and older and younger patients.

  • 11 DESCRIPTION

    Axatilimab-csfr is a CSF-1R–blocking antibody. Axatilimab-csfr is a humanized IgG4 (kappa light chain) monoclonal antibody produced in Chinese hamster ovary cells. Axatilimab-csfr has an approximate molecular weight of 150 kDa.

    NIKTIMVO (axatilimab-csfr) injection is a sterile, preservative-free, slightly opalescent, pale brownish yellow solution for intravenous use. The solution is free from visible particles.

    Each single-dose vial contains 50 mg of axatilimab-csfr in 1 mL of solution. Each mL contains 50 mg of axatilimab-csfr, citric acid monohydrate (3.6 mg), glycine (9.38 mg), polysorbate 80 (0.5 mg), sodium citrate (8.49 mg), sucrose (42.79 mg) and Water for Injection, USP. The pH is 5.0.

  • 12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    Axatilimab-csfr is a monoclonal antibody that binds to colony stimulating factor-1 receptors (CSF-1R) expressed on monocytes and macrophages. Blocking CSF-1R with axatilimab-csfr reduces the levels of these circulating proinflammatory and profibrotic monocytes and monocyte-derived macrophages, as demonstrated by a reduction of nonclassical monocyte counts in nonclinical studies with axatilimab-csfr, and inhibits the activity of pathogenic macrophages in tissues.

    12.2 Pharmacodynamics

    CSF-1 and Interleukin (IL)-34

    Axatilimab-csfr caused a dose-dependent increase from 0.15 mg/kg to 6 mg/kg (0.5 to 20 times the approved recommended dosage) in CSF-1 and interleukin (IL)-34 concentrations and a dose-dependent reduction in the levels of nonclassical monocytes in peripheral blood.

    12.3 Pharmacokinetics

    Axatilimab-csfr pharmacokinetics are presented as geometric mean (coefficient of variation [%CV]) in adult patients with cGVHD following axatilimab-csfr 0.3 mg/kg (maximum 35 mg) every 2 weeks, unless otherwise specified. Axatilimab-csfr AUC increased in a greater than dose-proportional manner following single-dose administration of axatilimab-csfr over a dose range of 0.15 mg/kg to 3 mg/kg (0.5 to 10 times the approved recommended dosage) in healthy subjects.

    There was no axatilimab-csfr systemic accumulation following the approved recommended dosage.

    Distribution

    Axatilimab-csfr volume of distribution is 6.06 L (16.3% CV).

    Elimination

    Axatilimab-csfr total clearance is 0.07 L/h (38.8% CV). The median (5th to 95th percentile) time to 97% reduction from Cmax after the end of infusion is 4.0 (2.3 to 7.2) days following axatilimab-csfr 0.3 mg/kg (maximum 35 mg).

    The total clearance of axatilimab-csfr is composed of linear and non-linear components such that axatilimab-csfr clearance decreased from 2.32 mL/h/kg to 0.21 mL/h/kg and mean terminal half-life increased from 10.7 hours to 108 hours following single-dose administrations of axatilimab-csfr over a dose range of 0.15 mg/kg to 3 mg/kg (0.5 to 10 times the approved recommended dosage).

    Metabolism

    Axatilimab-csfr is expected to be metabolized into small peptides by catabolic pathways.

    Specific Populations

    No clinically meaningful differences in the exposure of axatilimab-csfr were observed in adult and pediatric patients based on age (12 to 81 years), sex, body weight (40 to 151 kg), race (White, Black, or Asian), mild to moderate renal impairment (estimated creatinine clearance 30-89 mL/min by the Cockcroft-Gault equation), or mild hepatic impairment (total bilirubin ≤ ULN and AST > ULN or total bilirubin 1 to ≤ 1.5 times ULN and any AST) following the approved recommended dosage of 0.3 mg/kg (maximum 35 mg) every 2 weeks.

    The effect of severe renal impairment (estimated creatinine clearance 15-29 mL/min, Cockcroft-Gault equation) and moderate to severe hepatic impairment (total bilirubin > 1.5 times ULN and any AST) on axatilimab-csfr pharmacokinetics is unknown.

    Pediatric Patients

    Axatilimab-csfr exposures in pediatric patients weighing 40 kg and above are comparable to those in adults following the approved recommended dosage of 0.3 mg/kg (maximum 35 mg) every 2 weeks.

    12.6 Immunogenicity

    The observed incidence of ADAs is highly dependent on the sensitivity and specificity of the assay. Differences in assay methods preclude meaningful comparisons of the incidence of ADAs in the studies described below with the incidence of ADAs in other studies, including those of NIKTIMVO or of other axatilimab products.

    ADAs were assessed in 276 patients with cGVHD who received NIKTIMVO. The incidence of axatilimab-csfr treatment-emergent ADAs was 33.7% (93/276) following a median exposure time of 7.8 months. NAb were detected in 47 of 93 cGVHD patients with treatment-emergent ADAs. There was no clinically meaningful effect of anti–axatilimab-csfr antibodies or NAb on the pharmacokinetics, pharmacodynamics, or effectiveness of NIKTIMVO. The presence of NAb correlated with the occurrence of hypersensitivity reactions [see Adverse Reactions (6.1)].

  • 13 NONCLINICAL TOXICOLOGY

    13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

    No studies have been performed to assess the potential of axatilimab-csfr for carcinogenicity or genotoxicity.

    Dedicated fertility studies have not been conducted with axatilimab-csfr. Administration of axatilimab-csfr to sexually mature cynomolgus monkeys in a 3-month toxicology study had no effect on menstrual cyclicity in females, sperm parameters (morphology, motility, or number) in males, and produced no histopathologic findings in female and male reproductive organs, indicating that axatilimab-csfr did not adversely affect reproductive function. Targeted deletion of CSF-1R or CSF-1 in rodent models resulted in impairment of fertility.

    13.2 Animal Toxicology and/or Pharmacology

    In a 6-month chronic toxicity study in sexually immature cynomolgus monkeys, axatilimab-csfr was administered once weekly at doses of 10, 30, or 100 mg/kg/week via intravenous injection. The primary findings included periorbital swelling, widespread accumulation of basophilic material, and effects on bone at doses ≥ 10 mg/kg/week. Alterations in bone included decreases in bone markers, thickening of the growth plate and metaphysis and/or degeneration of the growth plate in the femur. In a 3-month toxicity study in sexually mature monkeys, intravenous administration of axatilimab-csfr at doses of 10, 30, or 100 mg/kg/week resulted in decreases in bone biomarkers at doses ≥ 30 mg/kg/week.

  • 14 CLINICAL STUDIES

    The efficacy of NIKTIMVO was evaluated in AGAVE-201 (NCT04710576), a randomized, open-label, multicenter study in adult and pediatric patients with recurrent or refractory cGVHD who had received at least 2 lines of systemic therapy and required additional treatment. Patients with platelet count ≥ 50 × 109/L, absolute neutrophil count ≥ 1 × 109/L, ALT and AST ≤ 2.5 × ULN (≤ 5 × ULN if liver cGVHD was present), total bilirubin ≤ 1.5 × ULN, and creatinine clearance ≥ 30 mL/minute were eligible. Patients with uncontrolled infections were not eligible.

    Treatment consisted of NIKTIMVO 0.3 mg/kg administered intravenously every 2 weeks until disease progression, lack of efficacy by 9 months, or unacceptable toxicity. Continued treatment with GVHD prophylaxis and standard care systemic cGVHD therapies were permitted as long as the patient had been on a stable dose for at least 2 weeks prior to study. Initiation of new systemic cGVHD therapy while on study was not permitted.

    Demographics and baseline characteristics of the 79 patients treated with NIKTIMVO 0.3 mg/kg every 2 weeks in AGAVE-201 are summarized in Table 4.

    Table 4: Demographics and Baseline Characteristics of Patients With cGVHD
  • * Prednisone equivalents/kilogram/day.
    		•

    NIKTIMVO
    0.3 mg/kg every 2 weeks
    (N = 79)

     Median age, years (range)

    		50 (7, 76)

            Age ≥ 65 years, n (%)

    		21 (27)

     Male, n (%)

    		46 (58)

     Race, n (%)

            White

    		67 (85)

            Asian

    		4 (5)

            Black

    		2 (3)

            Other

    		1 (1)

            Not reported

    		5 (6)

     Median (range) time (months) from cGVHD diagnosis

    		47 (4, 211)

     ≥ 4 Organs involved, n (%)

    		45 (57)

     Median (range) number of prior lines of therapy

    		4 (2, 12)

     Number of prior lines of therapy, n (%)

            2

    		11 (14)

            3

    		14 (18)

            4

    		17 (22)

            ≥ 5

    		37 (47)

     Prior cGVHD treatment with ibrutinib, n (%)

    		27 (34)

     Prior cGVHD treatment with ruxolitinib, n (%)

    		57 (72)

     Prior cGVHD treatment with belumosudil, n (%)

    		16 (20)

     Refractory to last therapy, n (%)

    		37 (47)

     Severe cGVHD, n (%)

    		63 (80)
     Median (range) Global Severity Rating 7 (2, 10)

     Median (range) modified Lee Symptom Scale Score at baseline

    		24 (4, 55)
     Median (range) corticosteroid dose at baseline (PE/kg)*
    		 0.21 (0.04, 2.12)

    The efficacy of NIKTIMVO was based on overall response rate (ORR) through Cycle 7 Day 1, where overall response included complete response or partial response according to the 2014 NIH Consensus Development Project on Response Criteria. The ORR results from AGAVE 201 for the 0.3 mg/kg every 2 weeks dosage regimen are presented in Table 5. The median time to first response was 1.5 months (range, 0.9 to 5.1 months). The median duration of response, calculated from first response to progression, death, or new systemic therapies for cGVHD, was 1.9 months (95% CI: 1.6, 3.5). In patients who achieved response, no death or new systemic therapy initiation occurred in 60% (95% CI: 43, 74) of patients for at least 12 months since response.

    Table 5: Efficacy Results From AGAVE-201
    CI = confidence interval

    Endpoint

    		NIKTIMVO
    0.3 mg/kg every 2 weeks
    (N = 79)

    Overall response rate, n (%)
    95% CI
        Complete response, n (%)
        Partial response, n (%)

    59 (75%)
    64, 84
    0 (0%)
    59 (75%)

    ORR results were supported by exploratory analyses of patient-reported symptom bother which showed at least a 7-point decrease in the modified Lee Symptom Scale score through Cycle 7 Day 1 in 56% (95% CI: 44, 67) of patients.

  • 16 HOW SUPPLIED/STORAGE AND HANDLING

    NIKTIMVO (axatilimab-csfr) injection is a slightly opalescent, pale brownish yellow solution. It is supplied in a carton containing one single-dose vial of:

    Store refrigerated at 2°C to 8°C (36°F to 46°F) in the original carton to protect from light. Do not freeze or shake.

  • 17 PATIENT COUNSELING INFORMATION

    Advise the patient to read the FDA-approved patient labeling (Patient Information).

    Infusion-Related Reactions

    Advise patients and caregivers that reactions related to the infusion may occur during NIKTIMVO treatment. Inform patients and caregivers of the signs and symptoms of infusion-related reactions and to seek medical care should signs and symptoms occur [see Warnings and Precautions (5.1)].

    Embryo-Fetal Toxicity

    Advise pregnant women of the potential risk to a fetus. Advise females of reproductive potential to inform their healthcare provider of a known or suspected pregnancy. Advise females of reproductive potential to use effective contraception during treatment with NIKTIMVO and for 30 days after the last dose [see Warnings and Precautions (5.2), Use in Specific Populations (8.1, 8.3)].

    Lactation

    Advise women not to breastfeed during treatment and for 30 days after the last dose of NIKTIMVO [see Use in Specific Populations (8.2)].

    Manufactured by:
    Incyte Corporation
    Wilmington, DE 19803
    U.S. License No.2228

    NIKTIMVO and the NIKTIMVO logo are trademarks of Incyte.
    Patent Information: www.incyte.com/patents
    © 2024 Incyte Corporation. All rights reserved.

  • PATIENT PACKAGE INSERT

    PATIENT INFORMATION
    NIKTIMVO™ (nik tim voe)
    (axatilimab-csfr)
    injection, for intravenous use

    What is NIKTIMVO?

    NIKTIMVO is a prescription medicine used to treat adults and children who weigh at least 88.2 pounds (40 kg) with chronic graft‑versus-host disease (cGVHD) after you have received at least 2 prior treatments (systemic therapy) and they did not work.

    It is not known if NIKTIMVO is safe and effective in adults and children weighing less than 88.2 pounds (40 kg).

    Before receiving NIKTIMVO, tell your healthcare provider about all of your medical conditions, including if you:

    • have or have had liver problems.
    • are pregnant or plan to become pregnant. NIKTIMVO may harm your unborn baby.
      Females who are able to become pregnant:
      • Your healthcare provider should do a pregnancy test before you start treatment with NIKTIMVO.
      • You should use an effective method of birth control during your treatment and for 30 days after your last dose of NIKTIMVO. Talk to your healthcare provider about birth control methods that you can use during this time.
      • Tell your healthcare provider right away if you become pregnant or think you may be pregnant during treatment with NIKTIMVO.
    • are breastfeeding or plan to breastfeed. It is not known if NIKTIMVO passes into your breast milk. Do not breastfeed during treatment and for 30 days after your last dose of NIKTIMVO.

    Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements.

    How will I receive NIKTIMVO?

    • Your healthcare provider will give you NIKTIMVO through an intravenous (IV) infusion over 30 minutes.
    • NIKTIMVO is given every 2 weeks.
    • Your healthcare provider will decide how many treatments you will need.
    • Before you receive each NIKTIMVO infusion, your healthcare provider may give you medicines called diphenhydramine and acetaminophen to help prevent infusion-related reactions.
    • Your healthcare provider will do blood tests to check you for side effects.

    What are the possible side effects of NIKTIMVO?

    NIKTIMVO may cause serious side effects, including:

    • Infusion-related reactions. Infusion-related reactions are common with NIKTIMVO and can be serious. Your healthcare provider will monitor you for infusion-related reactions during your treatment. If you have a reaction, your healthcare provider may temporarily or completely stop your treatment with NIKTIMVO. Tell your healthcare provider right away if you get fever, chills, rash, flushing, shortness of breath, trouble breathing, nausea, vomiting, or symptoms of high blood pressure such as chest pain, headaches, or blurred vision during an infusion of NIKTIMVO.

    The most common side effects of NIKTIMVO include:

    • infections
    • increased blood level of liver enzymes
    • decreased blood level of phosphate
    • low red blood cell count (anemia)
    • muscle, bone, or joint pain
    • increased blood level of pancreatic enzymes
    • low energy
    • increased blood level of calcium
    • increased blood level of a muscle enzyme
    • increased blood level of a bone enzyme
    • nausea
    • headache
    • diarrhea
    • cough
    • fever
    • shortness of breath
    These are not all the possible side effects of NIKTIMVO.
    Call your doctor for medical advice about side effects. You may report side effects to FDA at 1 800-FDA-1088.
    You may also report side effects to Incyte Corporation at 1-855-463-3463.
    General information about the safe and effective use of NIKTIMVO.
    Medicines are sometimes prescribed for purposes other than those listed in a Patient Information leaflet. You can ask your healthcare provider for information about NIKTIMVO that is written for health professionals.

    What are the ingredients in NIKTIMVO?
    Active ingredient: axatilimab-csfr
    Inactive ingredients: citric acid monohydrate, glycine, polysorbate 80, sodium citrate, sucrose, and Water for Injection.

    Manufactured by: Incyte Corporation, Wilmington, DE 19803
    U.S. License No.2228
    NIKTIMVO and the NIKTIMVO logo are trademarks of Incyte.
    © 2024 Incyte Corporation. All rights reserved.
    For more information, call 1-855-463-3463 or go to www.incyte.com/patents.

    This Patient Information has been approved by the U.S. Food and Drug Administration.                                      Issued: 8/2024

  • NIKTIMVO 50 MG/ML CARTON

    NDC: 50881-012-10
    Rx Only

    NIKTIMVO™
    (axatilimab-csfr)
    Injection
    50 mg/mL

    For intravenous infusion after dilution.
    Contains one 1 mL single-dose vial.
    Discard unused portion.

    NIKTIMVO 50 MG/ML CARTON

  • INGREDIENTS AND APPEARANCE
    NIKTIMVO 
    axatilimab-csfr injection
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 50881-012
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AXATILIMAB (UNII: R96Z451BMC) (AXATILIMAB - UNII:R96Z451BMC) AXATILIMAB50 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) 3.60 mg  in 1 mL
    SODIUM CITRATE (UNII: 1Q73Q2JULR) 8.49 mg  in 1 mL
    GLYCINE (UNII: TE7660XO1C) 9.38 mg  in 1 mL
    SUCROSE (UNII: C151H8M554) 42.79 mg  in 1 mL
    POLYSORBATE 80 (UNII: 6OZP39ZG8H) 0.50 mg  in 1 mL
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 50881-012-101 in 1 CARTON08/14/2024
    11 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BLABLA76141108/14/2024
    Labeler - Incyte Corporation (556967347)

    • Trademark Results [NIKTIMVO]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    NIKTIMVO
    NIKTIMVO
    98655051 not registered Live/Pending
    Incyte Holdings Corporation
    2024-07-18
    NIKTIMVO
    NIKTIMVO
    97672310 not registered Live/Pending
    Incyte Holdings Corporation
    2022-11-10
    © 2024 FDA.report
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