VUEWAY- gadopiclenol injection

Vueway by

Drug Labeling and Warnings

Vueway by is a Prescription medication manufactured, distributed, or labeled by BRACCO DIAGNOSTICS INC, Liebel-Flarsheim Company LLC, Guerbet. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

  • BOXED WARNING (What is this?)

    WARNING: RISK ASSOCIATED WITH INTRATHECAL USE and NEPHROGENIC SYSTEMIC FIBROSIS

    Risk Associated with Intrathecal Use
    Intrathecal administration of gadolinium-based contrast agents (GBCAs) can cause serious adverse reactions including death, coma, encephalopathy, and seizures. Vueway is not approved for intrathecal use [see Warnings and Precautions (5.1)].

    Nephrogenic Systemic Fibrosis
    GBCAs increase the risk for nephrogenic systemic fibrosis (NSF) among patients with impaired elimination of the drugs. Avoid use of Vueway in these patients unless the diagnostic information is essential and not available with non-contrasted MRI or other modalities. NSF may result in fatal or debilitating fibrosis affecting the skin, muscle and internal organs.

    • The risk for NSF appears highest among patients with:
      • Chronic, severe kidney disease (GFR < 30 mL/min/1.73 m2), or
      • Acute kidney injury.
    • Screen patients for acute kidney injury and other conditions that may reduce renal function. For patients at risk for chronically reduced renal function (e.g. age > 60 years, hypertension, diabetes), estimate the glomerular filtration rate (GFR) through laboratory testing.
    • For patients at highest risk for NSF, do not exceed the recommended Vueway dose and allow a sufficient period of time for elimination of the drug from the body prior to any re-administration [see Warnings and Precautions (5.2)].
  • 1  INDICATIONS AND USAGE

    Vueway® is indicated in adult and pediatric patients aged 2 years and older for use with magnetic resonance imaging (MRI) to detect and visualize lesions with abnormal vascularity in:

    • the central nervous system (brain, spine, and associated tissues),
    • the body (head and neck, thorax, abdomen, pelvis, and musculoskeletal system).
  • 2  DOSAGE AND ADMINISTRATION

    2.1  Recommended Dosage

    The recommended dose of Vueway for adult and pediatric patients aged 2 years and older is 0.05 mmol/kg actual body weight (equivalent to 0.1 mL/kg) administered intravenously at approximately 2 mL/sec.

    2.2  Administration and Imaging Instructions

    • Use aseptic technique for all handling and administration of Vueway.
    • Visually inspect Vueway for particulate matter and discoloration prior to administration. Do not use the solution if any particulate matter is present or the solution is discolored.
    • Do not mix with other medications because of the potential for chemical incompatibility.
    • Prime intravenous line before use.
    • Administer Vueway as an intravenous bolus injection, manually or by compatible power injector. The recommended injection rate is approximately 2 mL/second.
    • Flush the intravenous line with 0.9% Sodium Chloride Injection, USP after the administration of Vueway.
    • Contrast MRI can begin immediately following the injection of Vueway.

    2.3  Directions for Use of Single-Dose Vial and Pre-filled Syringe

    Vial

    • Do not pierce the rubber stopper more than once.
    • Aseptically draw up Vueway into a disposable syringe and use immediately.
    • If solidification occurs in the vial because of exposure to the cold, bring the vial of Vueway to room temperature before use and inspect that the solution is clear, colorless to yellow without any particulate matter and discoloration.
    • Discard any unused portion.

    Pre-filled syringe

    • Remove the tip cap of the syringe, screw the plunger rod and use immediately.
    • All luer connections should be gently hand tightened without over tightening, to ensure secure connections and to prevent damage to the device.
    • Pre-filled syringes must not be frozen. Frozen pre-filled syringes of Vueway should be discarded.
    • Discard any unused portion.

    2.4  Directions for Use of Pharmacy Bulk Package

    • Do not use the Pharmacy Bulk Package for direct infusion.
    • Perform the transfer of Vueway from the Pharmacy Bulk Package in an aseptic work area, such as laminar flow hood, using aseptic technique and suitable transfer device for filling empty syringes.
    • Penetrate the closure only one time. Once the container closure is punctured, do not remove the Pharmacy Bulk Package from the aseptic work area.
    • The Pharmacy Bulk Package is used with an appropriate transfer device for filling empty sterile syringes. Use each individual dose of Vueway promptly following withdrawal from the Pharmacy Bulk Package.
    • Use the contents of the Pharmacy Bulk Package within 24 hours at room temperature after initial puncture.
    • If solidification occurs in the vial because of exposure to the cold, bring the vial of Vueway to room temperature before use and inspect that the solution is clear, colorless to yellow without any particulate matter and discoloration.
  • 3  DOSAGE FORMS AND STRENGTHS

    Injection: Vueway is a clear, colorless to yellow aqueous solution at a concentration of 0.5 mmol/mL of gadopiclenol available as:

    StrengthPackaging
    • 1.5 mmol/3 mL (0.5 mmol/mL)
    • 3.75 mmol/7.5 mL (0.5 mmol/mL)
    • 5 mmol/10 mL (0.5 mmol/mL)
    • 7.5 mmol/15 mL (0.5 mmol/mL)
    		Single-dose vials (glass)
    • 3.75 mmol/7.5 mL (0.5 mmol/mL)
    • 5 mmol/10 mL (0.5 mmol/mL)
    • 7.5 mmol/15 mL (0.5 mmol/mL)
    		Single-dose prefilled syringes (plastic)
    • 15 mmol/30 mL (0.5 mmol/mL)
    • 25 mmol/50 mL (0.5 mmol/mL)
    • 50 mmol/100 mL (0.5 mmol/mL)
    		Pharmacy bulk package (glass)

  • 4  CONTRAINDICATIONS

    Vueway is contraindicated in patients with history of hypersensitivity reactions to Vueway.

  • 5  WARNINGS AND PRECAUTIONS

    5.1  Risk Associated with Intrathecal Use

    Intrathecal administration of GBCAs can cause serious adverse reactions including death, coma, encephalopathy, and seizures. The safety and effectiveness of Vueway have not been established with intrathecal use. Vueway is not approved for intrathecal use [see Dosage and Administration (2.1)].

    5.2  Nephrogenic Systemic Fibrosis

    GBCAs increase the risk for nephrogenic systemic fibrosis (NSF) among patients with impaired elimination of the drugs. Avoid use of Vueway among these patients unless the diagnostic information is essential and not available with non-contrast MRI or other modalities. The GBCA-associated NSF risk appears highest for patients with chronic, severe kidney disease (GFR <30 mL/min/1.73 m2) as well as patients with acute kidney injury. The risk appears lower for patients with chronic, moderate kidney disease (GFR 30-59 mL/min/1.73 m2) and little, if any, for patients with chronic, mild kidney disease (GFR 60-89 mL/min/1.73 m2). NSF may result in fatal or debilitating fibrosis affecting the skin, muscle, and internal organs. Report any diagnosis of NSF following Vueway administration to Bracco Diagnostics Inc. (1-800-257-5181) or FDA (1-800-FDA-1088 or www.fda.gov/medwatch).

    Screen patients for acute kidney injury and other conditions that may reduce renal function. Features of acute kidney injury consist of rapid (over hours to days) and usually reversible decrease in kidney function, commonly in the setting of surgery, severe infection, injury or drug-induced kidney toxicity. Serum creatinine levels and estimated GFR may not reliably assess renal function in the setting of acute kidney injury. For patients at risk for chronically reduced renal function (e.g., age >60 years, diabetes mellitus or chronic hypertension), estimate the GFR through laboratory testing.

    Among the factors that may increase the risk for NSF are repeated or higher than recommended doses of a GBCA and the degree of renal impairment at the time of exposure. Record the specific GBCA and the dose administered to a patient. For patients at highest risk for NSF, do not exceed the recommended Vueway dose and allow a sufficient period of time for elimination of the drug prior to re-administration. For patients receiving hemodialysis, physicians may consider the prompt initiation of hemodialysis following the administration of a GBCA in order to enhance the contrast agent’s elimination [see Use in Specific Populations (8.6) and Clinical Pharmacology (12.3)]. The usefulness of hemodialysis in the prevention of NSF is unknown.

    5.3  Hypersensitivity Reactions

    With GBCAs, serious hypersensitivity reactions have occurred. In most cases, initial symptoms occurred within minutes of GBCA administration and resolved with prompt emergency treatment.

    • Before Vueway administration, assess all patients for any history of a reaction to contrast media, bronchial asthma and/or allergic disorders. These patients may have an increased risk for a hypersensitivity reaction to Vueway.
    • Vueway is contraindicated in patients with history of hypersensitivity reactions to Vueway [see Contraindications (4)].
    • Administer Vueway only in situations where trained personnel and therapies are promptly available for the treatment of hypersensitivity reactions, including personnel trained in resuscitation.
    • During and following Vueway administration, observe patients for signs and symptoms of hypersensitivity reactions.

    5.4  Gadolinium Retention

    Gadolinium is retained for months or years in several organs. The highest concentrations (nanomoles per gram of tissue) have been identified in the bone, followed by other organs (e.g. brain, skin, kidney, liver, and spleen). The duration of retention also varies by tissue and is longest in bone. Linear GBCAs cause more retention than macrocyclic GBCAs. At equivalent doses, gadolinium retention varies among the linear agents with gadodiamide causing greater retention than other linear agents such as gadoxetate disodium and gadobenate dimeglumine. Retention is lowest and similar among the macrocyclic GBCAs such as gadoterate meglumine, gadobutrol, gadoteridol, and gadopiclenol.

    Consequences of gadolinium retention in the brain have not been established. Pathologic and clinical consequences of GBCA administration and retention in skin and other organs have been established in patients with impaired renal function [see Warnings and Precautions (5.2)]. There are rare reports of pathologic skin changes in patients with normal renal function. Adverse events involving multiple organ systems have been reported in patients with normal renal function without an established causal link to gadolinium.

    While clinical consequences of gadolinium retention have not been established in patients with normal renal function, certain patients might be at higher risk. These include patients requiring multiple lifetime doses, pregnant and pediatric patients, and patients with inflammatory conditions. Consider the retention characteristics of the agent when choosing a GBCA for these patients. Minimize repetitive GBCA imaging studies, particularly closely spaced studies, when possible.

    5.5  Acute Kidney Injury

    In patients with chronically reduced renal function, acute kidney injury requiring dialysis has occurred with the use of GBCAs. The risk of acute kidney injury may increase with increasing dose of the contrast agent. Do not exceed the recommended dose.

    5.6  Extravasation and Injection Site Reactions

    Injection site reactions such as injection site pain have been reported in the clinical studies with Vueway [see Adverse Reactions (6.1)]. Extravasation during Vueway administration may result in tissue irritation [see Nonclinical Toxicology (13.2)]. Ensure catheter and venous patency before the injection of Vueway.

    5.7  Interference with Visualization of Lesions Visible with Non-Contrast MRI

    As with any GBCA, Vueway may impair the visualization of lesions seen on non-contrast MRI. Therefore, caution should be exercised when Vueway MRI scans are interpreted without a companion non-contrast MRI scan.

  • 6  ADVERSE REACTIONS

    The following serious adverse reactions are discussed elsewhere in labeling:

    • Nephrogenic Systemic Fibrosis [see Warnings and Precautions (5.2)]
    • Hypersensitivity Reactions [see Contraindications (4) and Warnings and Precautions (5.3)]

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

    The safety of Vueway was evaluated in 1,047 patients who received Vueway at doses ranging from 0.025 mmol/kg (one half the recommended dose) to 0.3 mmol/kg (six times the recommended dose). A total of 708 patients received the recommended dose of 0.05 mmol/kg. Among patients who received the recommended dose, the average age was 51 years (range 2 years to 88 years) and 56% were female. The ethnic distribution was 79% White, 10% Asian, 7% American Indian or Alaska native, 2% Black, and 2% patients of other or unspecified ethnic groups.

    Overall, approximately 4.7% of subjects receiving the labeled dose reported one or more adverse reactions.

    Table 1 lists adverse reactions that occurred in > 0.2% of patients who received 0.05 mmol/kg Vueway.

    Table 1. Adverse Reactions Reported in > 0.2% of Patients Receiving Vueway in Clinical Trials
    Adverse ReactionVueway 0.05 mmol/kg
    (n=708)
    (%)
    Injection site pain0.7
    Headache0.7
    Nausea0.4
    Injection site warmth0.4
    Injection site coldness0.3
    Dizziness0.3
    Localized swelling0.3

    Adverse reactions that occurred with a frequency ≤ 0.2% in patients who received 0.05 mmol/kg Vueway included: maculopapular rash, vomiting, worsened renal impairment, feeling hot, pyrexia, oral paresthesia, dysgeusia, diarrhea, pruritus, allergic dermatitis, erythema, injection site paresthesia, Cystatin C increase, and blood creatinine increase.

    Adverse Reactions in Pediatric Patients
    One study with a single dose of Vueway (0.05 mmol/kg) was conducted in 80 pediatric patients aged 2 years to 17 years, including 60 patients who underwent a central nervous system (CNS) MRI and 20 patients who underwent a body MRI. One adverse reaction (maculopapular rash of moderate severity) in one patient (1.3%) was reported in the CNS cohort.

  • 8  USE IN SPECIFIC POPULATIONS

    8.1  Pregnancy

    Risk Summary
    There are no available data on Vueway use in pregnant women to evaluate for a drug-associated risk of major birth defects, miscarriage or other adverse maternal or fetal outcomes. GBCAs cross the human placenta and result in fetal exposure and gadolinium retention. The available human data on GBCA exposure during pregnancy and adverse fetal outcomes are limited and inconclusive (see Data).

    In animal reproduction studies, there were no adverse developmental effects observed in rats or rabbits with intravenous administration of Vueway during organogenesis (see Data).

    Because of the potential risks of gadolinium to the fetus, use Vueway only if imaging is essential during pregnancy and cannot be delayed.

    The estimated background risk of major birth defects and miscarriage for the indicated population(s) are 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 and miscarriage in clinically recognized pregnancies is 2% to 4% and 15% to 20% respectively.

    Data
    Human Data
    Contrast enhancement is visualized in the placenta and fetal tissues after maternal GBCA administration.

    Cohort studies and case reports on exposure to GBCAs during pregnancy have not reported a clear association between GBCAs and adverse effects in the exposed neonates. However, a retrospective cohort study comparing pregnant women who had a GBCA MRI to pregnant women who did not have an MRI reported a higher occurrence of stillbirths and neonatal deaths in the group receiving GBCA MRI. Limitations of this study include a lack of comparison with non-contrast MRI and lack of information about the maternal indication for MRI. Overall, these data preclude a reliable evaluation of the potential risk of adverse fetal outcomes with the use of GBCAs in pregnancy.

    Animal Data
    Gadolinium Retention: GBCAs administered to pregnant non-human primates (0.1 mmol/kg on gestational days 85 and 135) result in measurable gadolinium concentration in the offspring in bone, brain, skin, liver, kidney, and spleen for at least 7 months. GBCAs administered to pregnant mice (2 mmol/kg daily on gestational days 16 through 19) result in measurable gadolinium concentrations in the pups in bone, brain, kidney, liver, blood, muscle, and spleen at one-month postnatal age.

    Reproductive Toxicology: Animal reproduction studies conducted with gadopiclenol showed some signs of maternal toxicity in rats at 10 mmol/kg and rabbits at 5 mmol/kg (corresponding to 52 times and 57 times the recommended human dose, respectively). This maternal toxicity was characterized in both species by swelling, decreased activity, and lower gestation weight gain and food consumption.

    No effect on embryo-fetal development was observed in rats at 10 mmol/kg (corresponding to 52 times the recommended human dose). In rabbits, a lower mean fetal body weight was observed at 5 mmol/kg (corresponding to 57 times the recommended human dose) and this was attributed as a consequence of the lower gestation weight gain.

    8.2  Lactation

    Risk Summary
    There are no data on the presence of gadopiclenol in human milk, the effects on the breastfed infant, or the effects on milk production. However, published lactation data on other GBCAs indicate that 0.01% to 0.04% of the maternal gadolinium dose is excreted in breast milk. Additionally, there is limited GBCA gastrointestinal absorption in the breast-fed infant. Gadopiclenol is present in rat milk. When a drug is present in animal milk, it is likely that the drug will be present in human milk (see Data). The developmental and health benefits of breastfeeding should be considered along with the mother’s clinical need for Vueway and any potential adverse effects on the breastfed infant from Vueway or from the underlying maternal condition.

    Data
    In lactating rats receiving single intravenous injection of [153Gd]-gadopiclenol, 0.3% and 0.2% of the total administered radioactivity was transferred to the pups via maternal milk at 6 hours and 24 hours after administration, respectively. Furthermore, in nursing rat pups, oral absorption of gadopiclenol was 3.6%.

    8.4  Pediatric Use

    The safety and effectiveness of Vueway for use with MRI to detect and visualize lesions with abnormal vascularity in the CNS (brain, spine, and associated tissues), and the body (head and neck, thorax, abdomen, pelvis, and musculoskeletal system) have been established in pediatric patients aged 2 years and older.

    Use of Vueway in this age group is supported by evidence from adequate and well-controlled studies in adults with additional pharmacokinetic and safety data from an open-label, uncontrolled, multicenter, single dose study of Vueway (0.05 mmol/kg) in 80 pediatric patients aged 2 to 17 years. The 80 patients consisted of 60 patients who underwent a CNS MRI and 20 patients who underwent a body MRI [see Adverse Reactions (6.1) and Clinical Pharmacology (12.3)].

    The safety and effectiveness of Vueway have not been established in pediatric patients younger than 2 years of age.

    8.5  Geriatric use

    Of the total number of Vueway-treated patients in clinical studies, 270 (26%) patients were 65 years of age and over, while 62 (6%) patients were 75 years of age and over. No overall differences in safety or efficacy were observed between these subjects and younger subjects.

    This drug is known to be substantially excreted by the kidney, and the risk of adverse reactions to this drug may be greater in patients with impaired renal function. Because elderly patients are more likely to have decreased renal function, it may be useful to monitor renal function.

    8.6  Renal impairment

    In patients with renal impairment, the exposure of gadopiclenol is increased compared to patients with normal renal function. This may increase the risk of adverse reactions such as nephrogenic systemic fibrosis (NSF). Avoid use of GBCAs among these patients unless the diagnostic information is essential and not available with non-contrast MRI or other modalities. No dose adjustment of Vueway is recommended for patients with renal impairment. Vueway can be removed from the body by hemodialysis [see Warnings and Precautions (5.2, 5.4, 5.5) and Clinical Pharmacology (12.3)].

  • 10  OVERDOSAGE

    Among subjects who received a single 0.3 mmol/kg intravenous dose of gadopiclenol (6 times the recommended dose of Vueway), headache and nausea were the most frequently reported adverse reactions. Gadopiclenol can be removed from the body by hemodialysis [see Clinical Pharmacology (12.3)].

  • 11  DESCRIPTION

    Vueway is a gadolinium-based contrast agent, which contains gadopiclenol, a paramagnetic macrocyclic non-ionic complex of gadolinium.

    The chemical name for gadopiclenol is rac-[(2R,2'Ξ,2''Ξ)-2,2',2''-(3,6,9-triaza-κ3N3,N6,N9-1(2,6)-pyridina-κN1-cyclodecaphane-3,6,9-triyl)tris(5-{[(2Ξ)-2,3-dihydroxypropyl]amino}-5-oxopentanoato-κ3O1,O1',O1'')(3−)]gadolinium with a molecular weight of 970.11 g/mol and a molecular formula of C35H54GdN7O15.

    Gadopiclenol Structure

    Vueway is a sterile, nonpyrogenic, clear, colorless to yellow aqueous solution for intravenous use.

    Each mL contains 485.1 mg of gadopiclenol (equivalent to 0.5 mmol of gadopiclenol and 78.6 mg of gadolinium) and the following inactive ingredients: 0.404 mg tetraxetan, 1.211 mg trometamol, hydrochloric acid and/or sodium hydroxide (for pH adjustment, if needed), and water for injection.

    The main physicochemical properties of Vueway are provided in Table 2.

    Table 2: Physicochemical properties of Vueway
    ParameterValue
    Density at 20°C1.211 g/cm3
    Mean viscosity at 20°C12.6 mPa.s
    Mean viscosity at 37°C7.6 mPa.s
    Osmolality at 37°C850 mOsm/kg water
    pH7.0 – 7.8

  • 12  CLINICAL PHARMACOLOGY

    12.1  Mechanism of Action

    Gadopiclenol is a paramagnetic molecule (macrocyclic non-ionic complex of gadolinium) that develops a magnetic moment when placed in a magnetic field. The magnetic moment alters the relaxation rates of water protons in its vicinity in the body, leading to an increase in signal intensity (brightness) of tissues.

    12.2  Pharmacodynamics

    In MRI, visualization of normal and pathological tissue depends in part on variations in the radiofrequency signal intensity that occur with:

    • differences in proton density
    • differences of the spin-lattice or longitudinal relaxation times (T1)
    • differences in the spin-spin or transverse relaxation time (T2).

    When placed in a magnetic field (patient in MRI machine), gadopiclenol shortens the T1 and T2 relaxation times in targeted tissues. The extent to which a contrast agent can affect the relaxation rate of tissue water (1/T1 or 1/T2) is termed relaxivity (r1 or r2).

    The relaxivity of GBCAs is presented in Table 3.

    Table 3. Relaxivity (r1) of GBCAs in Human Plasma/Serum at 1.5 T and 37°C
    Gadolinium-Chelater1 (L.mmol-1.s-1)
    Gadobenic acid6.3
    Gadobutrol5.2
    Gadodiamide4.3
    Gadopentetic acid4.1
    Gadopiclenol12.8
    Gadoteric acid3.6
    Gadoteridol4.1
    Gadoxetic acid6.9

    Cardiac Electrophysiology
    At 6 times the recommended dosage in adult patients, gadopiclenol does not prolong the QT interval to any clinically relevant extent.

    12.3  Pharmacokinetics

    The Cmax and AUCinf of gadopiclenol increased proportionally over a dosage range from 0.025 mmol/kg to 0.3 mmol/kg (0.5 times to 6 times the recommended dosage). At the recommended dose, the mean (CV%) Cmax and AUCinf were 525 (13%) µg/mL and 569 (18%) µg·h/mL, respectively.

    Distribution
    After intravenous administration of Vueway, gadopiclenol is distributed in the extracellular fluids.

    The mean (CV%) volume of distribution of gadopiclenol at steady state is 13 (13%) L.

    Protein binding of gadopiclenol is ≤ 1.8% at clinically relevant concentrations.

    Following GBCA administration, gadolinium is present for months or years in brain, bone, skin, and other organs [see Warnings and Precautions (5.4)]. It is unknown whether the recommended dose of Vueway results in similar or different levels of gadolinium retention relative to those of other approved macrocyclic GBCAs at their recommended doses.

    Elimination
    The mean (CV%) elimination half-life (t1/2) of gadopiclenol is 1.5 (14%) hour.

    The mean (CV%) total body clearance (CL) and renal clearance (CLr) of gadopiclenol are 100 (9.5%) mL/min and 81 (35%) mL/min, respectively.

     Metabolism
     Gadopiclenol is not metabolized.

     Excretion
     Gadopiclenol is mainly eliminated through the kidneys by glomerular filtration. Approximately 98% of the dose was recovered in urine within 48 hours after administration.

    Specific Populations
    No clinically significant differences in the pharmacokinetics of gadopiclenol were observed based on sex.

    Pediatric Patients
    The pharmacokinetics of gadopiclenol for pediatric patients (2 to 17 years of age) were within range to those of adults (> 18 years of age) [see Dosage and Administration (2.1)].

    The pharmacokinetic parameters (median [range]) of gadopiclenol in pediatric patients are presented in Table 4.

    Table 4. Pharmacokinetic Parameters (Median [Range])a According to Age Classes
    aAt the recommended dosage
     2-6 years7–11 years12–17 years>18 years
    CL (L/h/kg)0.12 [0.05; 0.28]0.10 [0.04; 0.24]0.08 [0.04; 0.20]0.08 [0.05; 0.14]
    t1/2 (h)1.29 [0.69; 3.38]1.48 [0.83; 3.20]1.77 [1.00; 3.57]1.82 [0.93; 3.68]
    AUCinf (µgh/mL)403 [169; 964]478 [183; 1077]582 [267; 12901]590 [353; 937]
    C20 (µg/mL)236 [136; 387]260 [151; 401]286 [155; 441]296 [166; 485]

    Patients with Renal Impairment
    The pharmacokinetic parameters (mean (%CV)) of gadopiclenol in patients with renal impairment are presented in Table 5.

    Table 5. Effect of Renal Impairment on the Pharmacokinetics of Gadopiclenola,b
    aFollowing administration of a single gadopiclenol 0.1 mmol/kg dose (2 times the recommended dosage).
    beGFR: estimate of GFR based on an estimation equation and expressed in mL/min. To convert mL/min/1.73 m2 to mL/min, multiply by the individual’s BSA and divide by 1.73.
     Normal (eGFR ≥ 90 mL/min)Mild (eGFR 60 to < 90 mL/min)Moderate (eGFR 30 to < 60 mL/min)Severe (eGFR 15 to < 30 mL/min)
    AUCinf (µgh/mL)1113 (24%)1711 (31%)2759 (28%)9671 (18%)
    CLr (mL/min)96 (10%)76 (23%)44 (25%)14 (26%)
    t1/2 (h)1.93.33.811.7

    In patients with mild or moderate renal impairment, more than 90% of the administered Vueway was recovered in urine within 48 hours. In patients with severely impaired renal function about 84% of the administered Vueway was recovered in urine within 5 days.

    In patients with eGFR < 15 mL/min, hemodialysis effectively removed gadopiclenol from plasma as the percentage of decrease in blood concentrations was 95 to 98% at the end of the first hemodialysis session and 100% after the third hemodialysis session [see Warnings and Precautions (5.2), Use in Specific Populations (8.6)].

  • 13  NONCLINICAL TOXICOLOGY

    13.1  Carcinogenesis, Mutagenesis, Impairment of Fertility

    Carcinogenesis
    No carcinogenicity studies of gadopiclenol were performed.

    Mutagenesis
    Gadopiclenol did not demonstrate mutagenic potential in in vitro bacterial reverse mutation assays (Ames test), in an in vitro chromosome aberration assay in Chinese hamster ovary cells nor in an in vivo rat micronucleus assay.

    Impairment of Fertility
    Gadopiclenol had no effect on fertility and general reproductive performance of male and female rats when given at dose up to 10 mmol/kg (corresponding to 62 times the recommended human dose).

    13.2  Animal Toxicology

    Local intolerance reactions, including slight to moderate erythema and edema, were observed after perivenous injection in rabbits suggesting the possibility of local irritation if the contrast medium leaks around the veins in a clinical setting [see Warnings and Precautions (5.6)].

  • 14  CLINICAL STUDIES

    14.1  Overview of Clinical Studies

    The safety and effectiveness of Vueway for lesion visualization were evaluated in two prospective, double blind, randomized, crossover clinical studies. Study 1 (NCT03996447) was performed in adults with known or highly suspected CNS lesions with focal areas of disruption of the blood-brain barrier. Study 2 (NCT03986138) was performed in adults with suspected enhancing abnormalities in at least one body region among the head and neck, thorax, abdomen, pelvis, and musculoskeletal system.

    In each study, patients received both Vueway 0.05 mmol/kg and gadobutrol 0.1 mmol/kg (as an active comparator) in random order separated by 2 days to 14 days. Magnetic resonance imaging was performed before and after administration of each contrast agent.

    Pre-contrast and paired (consisting of both pre-contrast and post-contrast images for the same drug) image sets were independently evaluated by three central readers who were blinded to identity of the contrast agent. Readers scored up to three lesions per patient for border delineation, internal morphology, and contrast enhancement, each on a scale from 1 to 4. The total number of lesions was also reported. An additional independent central reader performed lesion tracking to allow matching of lesions between pre-contrast and paired images.

    The analysis compared the patient-level average score for matching lesions for each visualization parameter between pre-contrast and paired image sets.

    14.2  Visualization of CNS Lesions

    Study 1 included 256 patients with known or highly suspected CNS lesion(s). Among the enrolled patients, 239 had assessable pre-contrast and paired images with at least one matching lesion for at least one reader. These patients had a mean age of 57 years (range: 18 years to 84 years), 52% were female, and 83% were White.

    All three blinded readers’ evaluations of paired pre-contrast plus post-contrast images and pre-contrast images alone for all lesion visualization criteria, the pre-specified co-primary efficacy endpoints, are presented in Table 6.

    Table 6. Patient-Level CNS Lesion Visualization Scores by Reader, Paired vs. Pre-contrast in Patients Receiving Vueway 0.05 mmol/kg Intravenously
    LS: Least Squares; SE: Standard Error; CI: Confidence Interval.
    Only matching lesions are considered. The mixed models based on the full analysis set (N=239) include lesion visualization factor as dependent variable, MRI modality (Pre-contrast and Paired MRI) as fixed factors, and patient as a random factor.
    *p<0.0001 for all rows
     nLS Mean (SE)95% CI difference 
    PairedPreDifference
    Border delineation
    Reader 12273.90 (0.02)2.08 (0.02)1.82 (0.03)(1.76, 1.88) 
    Reader 22293.64 (0.04)1.74 (0.04)1.90 (0.05)(1.81, 2.00) 
    Reader 32023.97 (0.03)2.61 (0.03)1.36 (0.04)(1.29, 1.44) 
    Internal morphology
    Reader 12273.92 (0.03)1.66 (0.03)2.26 (0.03)(2.20, 2.33) 
    Reader 22293.65 (0.03)1.88 (0.03)1.77 (0.04)(1.69, 1.85) 
    Reader 32023.97 (0.04)2.01 (0.04)1.96 (0.05)(1.85, 2.06) 
    Degree of contrast enhancement
    Reader 12273.77 (0.03)1.00 (0.03)2.77 (0.04)(2.69, 2.85) 
    Reader 22293.58 (0.03)1.00 (0.03)2.58 (0.05)(2.49, 2.67) 
    Reader 32023.90 (0.02)1.00 (0.02)2.90 (0.03)(2.84, 2.95) 

    Gadopiclenol lesion visualization scores and number of lesions identified per patient were similar to those for gadobutrol.

    14.3  Visualization of Body Lesions

    Study 2 included 304 patients presenting with known or suspected enhancing abnormality(ies) and/or lesion(s) in at least one region among the head and neck, musculoskeletal system including extremities, and body including thorax, abdomen, and pelvis. Among the enrolled patients, 278 had assessable pre-contrast and paired images with at least one matching lesion for at least one reader. These patients had a mean age of 57 years (range: 21 years to 86 years), 59% were female, and 71% were White.

    Three readers assessed images of the head and neck, three other readers assessed images of the musculoskeletal system, and another three readers assessed other areas collectively referred to as the body (thorax, abdomen, and pelvis). Lesion visualization scores by reader in each anatomic region at patient-level as supportive analyses are summarized in Table 7.

    Table 7. Patient-Level Body Lesion Visualization Scores by Reader and Anatomic Region, Paired vs. Pre-contrast in Patients Receiving Vueway 0.05 mmol/kg Intravenously
    LS: Least Squares; SE: Standard Error; CI: Confidence Interval.
    Only matching lesions are considered. The mixed models based on the full analysis set (N=278) include lesion visualization factor as a dependent variable, patient as a random factor, and MRI modality (Pre-contrast and Paired MRI), body regions, and MRI body regions as fixed factors.
     nLS Mean (SE)95% CI difference
    PairedPre-contrastDifference
    Head & Neck
    Border delineation
    Reader 1153.71 (0.10)2.13 (0.10)1.58 (0.14)(1.30, 1.86)
    Reader 2193.53 (0.18)2.11 (0.18)1.42 (0.18)(1.06, 1.78)
    Reader 3133.92 (0.13)2.85 (0.13)1.08 (0.13)(0.82, 1.33)
    Internal morphology
    Reader 1153.80 (0.07)1.87 (0.07)1.93 (0.10)(1.74, 2.12)
    Reader 2193.74 (0.14)2.05 (0.14)1.68 (0.16)(1.37, 2.00)
    Reader 3133.92 (0.12)2.54 (0.12)1.38 (0.14)(1.10, 1.67)
    Degree of contrast enhancement
    Reader 1153.60 (0.11)1.00 (0.11)2.60 (0.16)(2.29, 2.91)
    Reader 2193.68 (0.16)1.00 (0.16)2.68 (0.22)(2.22, 3.15)
    Reader 3133.92 (0.11)1.00 (0.11)2.92 (0.15)(2.61, 3.24)
    Musculoskeletal system (including extremities)
    Border delineation
    Reader 1173.00 (0.10)2.06 (0.10)0.94 (0.13)(0.68, 1.20)
    Reader 2172.68 (0.20)2.44 (0.20)0.24 (0.19)(-0.15, 0.62)
    Reader 3212.81 (0.10)2.05 (0.10)0.76 (0.10)(0.56, 0.96)
    Internal morphology
    Reader 1173.00 (0.07)2.00 (0.07)1.00 (0.09)(0.82, 1.18)
    Reader 2173.94 (0.15)2.35 (0.15)1.59 (0.17)(1.25, 1.92)
    Reader 3212.90 (0.09)2.05 (0.09)0.86 (0.11)(0.64, 1.08)
    Degree of contrast enhancement
    Reader 1172.82 (0.10)1.00 (0.10)1.82 (0.15)(1.53, 2.12)
    Reader 2173.33 (0.17)1.00 (0.17)2.33 (0.24)(1.847, 2.82)
    Reader 3213.06 (0.08)1.00 (0.08)2.06 (0.12)(1.82, 2.31)
    Body (thorax, abdomen, pelvis)
    Border delineation
    Reader 12193.86 (0.03)2.28 (0.03)1.57 (0.04)(1.50, 1.64)
    Reader 21943.54 (0.06)3.15 (0.06)0.40 (0.06)(0.29, 0.51)
    Reader 32283.53 (0.03)1.69 (0.03)1.84 (0.03)(1.78, 1.90)
    Internal morphology
    Reader 12193.86 (0.02)2.00 (0.02)1.87 (0.03)(1.82, 1.92)
    Reader 21943.74 (0.05)3.41 (0.05)0.33 (0.05)(0.23, 0.43)
    Reader 32283.78 (0.03)1.60 (0.03)2.17 (0.03)(2.11, 2.24)
    Degree of contrast enhancement
    Reader 12193.71 (0.03)1.00 (0.03)2.71 (0.04)(2.63, 2.79)
    Reader 21942.69 (0.05)1.00 (0.05)1.69 (0.07)(1.54, 1.83)
    Reader 32283.33 (0.03)1.00 (0.03)2.33 (0.44)(2.25, 2.40)

    Gadopiclenol lesion visualization scores and number of lesions identified per patient were similar to those for gadobutrol.

  • 16  HOW SUPPLIED/STORAGE AND HANDLING

    HOW SUPPLIED
    Vueway is a clear, colorless to yellow aqueous solution supplied in the following presentations:

    StrengthSale UnitNDC
    Single-Dose Vial (glass)
    1.5 mmol/3 mL
    (0.5 mmol/mL)    		Carton of 10270-7020-37
    Carton of 100270-7020-38
    3.75 mmol/7.5 mL
    (0.5 mmol/mL)    		Carton of 10270-7025-39
    Carton of 100270-7025-40
    5 mmol/10 mL
    (0.5 mmol/mL)    		Carton of 10270-7030-41
    Carton of 100270-7030-42
    7.5 mmol/15 mL
    (0.5 mmol/mL)    		Carton of 10270-7035-43
    Carton of 100270-7035-44
    Single-Dose Prefilled Syringe (plastic)
    3.75 mmol/7.5 mL
    (0.5 mmol/mL)    		Carton of 10270-7040-43
    Carton of 100270-7040-44
    5 mmol/10 mL
    (0.5 mmol/mL)    		Carton of 10270-7045-45
    Carton of 100270-7045-46
    7.5 mmol/15 mL
    (0.5 mmol/mL)    		Carton of 10270-7050-47
    Carton of 100270-7050-48
    Pharmacy Bulk Package (glass)
    15 mmol/30 mL
    (0.5 mmol/mL)    		Carton of 10270-7015-45
    Carton of 250270-7015-46
    25 mmol/50 mL
    (0.5 mmol/mL)    		Carton of 10270-7015-47
    Carton of 250270-7015-48
    50 mmol/100 mL
    (0.5 mmol/mL)    		Carton of 10270-7015-63
    Carton of 60270-7015-64
    Carton of 120270-7015-65

    Storage and Handling
    Store at 25°C (77°F); excursions permitted from 15°C to 30°C (59°F to 86°F) [see USP, Controlled Room Temperature].

    Do not freeze Pre-filled syringes.

  • 17  PATIENT COUNSELING INFORMATION

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

    Nephrogenic Systemic Fibrosis

    Inform the patient that Vueway may increase the risk for NSF among patients with impaired elimination of the drugs and that NSF may result in fatal or debilitating fibrosis affecting the skin, muscle and internal organs.

    Instruct the patients to contact their physician if they develop signs or symptoms of NSF following Vueway administration, such as burning, itching, swelling, scaling, hardening and tightening of the skin; red or dark patches on the skin; stiffness in joints with trouble moving, bending or straightening the arms, hands, legs or feet; pain in the hip bones or ribs; or muscle weakness [see Warnings and Precautions (5.2)].

    Gadolinium Retention

    Advise patients that gadolinium is retained for months or years in brain, bone, skin, and other organs following Vueway administration even in patients with normal renal function. The clinical consequences of retention are unknown. Retention depends on multiple factors and is greater following administration of linear GBCAs than following administration of macrocyclic GBCAs [see Warnings and Precautions (5.4)].

    Injection Site Reactions

    Inform the patient that Vueway may cause reactions along the venous injection site, such as mild and transient burning or pain or feeling of warmth or coldness at the injection site [see Warnings and Precautions (5.6)].

    Pregnancy

    Advise pregnant women of the potential risk of fetal exposure to Vueway [see Use in Specific Populations (8.1)].

    CL121A02
    Revised: 01/2024

    Manufactured for
    Bracco Diagnostics Inc.
    Monroe Township, NJ 08831
    by
    Liebel-Flarsheim Company LLC,
    8800 Durant Road, Raleigh, North Carolina (NC) 27616-3104, USA

  • MEDICATION GUIDE

    This Medication Guide has been approved by the U.S. Food and Drug Administration.Revised: 1/2024
    MEDICATION GUIDE
    Vueway (VIEW-way)
    (gadopiclenol)
    injection, for intravenous use
    What is Vueway?
    • Vueway is a prescription medicine called a gadolinium-based contrast agent (GBCA). Vueway, like other GBCAs, is injected into your vein and used with a magnetic resonance imaging (MRI) scanner.
    • An MRI exam with a GBCA, including Vueway, helps your healthcare provider to see problems better than an MRI exam without a GBCA.
    • Your healthcare provider has reviewed your medical records and has determined that you would benefit from using a GBCA with your MRI exam.
    What is the most important information I should know about Vueway?
    • GBCAs like Vueway may cause serious side effects including death, coma, encephalopathy, and seizures when it is given intrathecally (injection given into the spinal canal). It is not known if Vueway is safe and effective with intrathecal use. Vueway is not approved for this use.
    • Vueway contains a metal called gadolinium. Small amounts of gadolinium can stay in your body including the brain, bones, skin and other parts of your body for a long time (several months to years).
    • It is not known how gadolinium may affect you, but so far, studies have not found harmful effects in patients with normal kidneys.
    • Rarely patients have reported pains, tiredness, and skin, muscle or bone ailments for a long time, but these symptoms have not been directly linked to gadolinium.
    • There are different GBCAs that can be used for your MRI exam. The amount of gadolinium that stays in the body is different for different gadolinium medicines. Gadolinium stays in the body more after gadodiamide than after gadoxetate disodium or gadobenate dimeglumine. Gadolinium stays in the body the least after, gadoterate meglumine, gadobutrol, gadoteridol, and gadopiclenol.
    • People who get many doses of gadolinium medicines, women who are pregnant and young children may be at increased risk from gadolinium staying in the body.
    • Some people with kidney problems who get gadolinium medicines can develop a condition with severe thickening of the skin, muscles and other organs in the body (nephrogenic systemic fibrosis). Your healthcare provider should screen you to see how well your kidneys are working before you receive Vueway.
    Do not receive Vueway if you have had a severe allergic reaction to Vueway.
    Before receiving Vueway, tell your healthcare provider about all your medical conditions, including if you:
    • have had any MRI procedures in the past where you received a GBCA. Your healthcare provider may ask you for more information including the dates of these MRI procedures.
    • are pregnant or plan to become pregnant. It is not known if Vueway can harm your unborn baby. Talk to your healthcare provider about the possible risks to an unborn baby if a GBCA such as Vueway is received during pregnancy.
    • have kidney problems, diabetes, or high blood pressure.
    • have had an allergic reaction to dyes (contrast agents) including GBCAs.
    What are possible side effects of Vueway?
    • See “What is the most important information I should know about Vueway?”
    • Allergic reactions. Vueway can cause allergic reactions that can sometimes be serious. Your healthcare provider will monitor you closely for symptoms of an allergic reaction.
    The most common side effects of Vueway include: injection site pain, headache, nausea, injection site coldness, injection site warmth, dizziness, and localized swelling.
    These are not all the possible side effects of Vueway.
    Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
    General information about the safe and effective uses of Vueway.
    Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. You can ask your healthcare provider for information about Vueway that is written for health professionals.
    What are the ingredients in Vueway?
    Active ingredient: gadopiclenol
    Inactive ingredients: tetraxetan; trometamol; hydrochloric acid or sodium hydroxide for pH adjustment; and water for injection
    Manufactured for Bracco Diagnostics Inc.
    by: Liebel-Flarsheim Company LLC, 8800 Durant Road, Raleigh, North Carolina (NC) 27616-3104, USA
    Distributed by: Bracco Diagnostics Inc., 259 Prospect Plains Road, Monroe Township, New Jersey 08831, USA


    For more information, go to www.imaging.bracco.com or call 800-257-5181.

    CL121A02

  • PRINCIPAL DISPLAY PANEL

    3 mL Internal Label

    3 mL Internal Label

    3 mL External Label

    3 mL External Label

    30 mL Internal Label

    30 mL Internal Label

    30 mL External Label

    30 mL External Label

    100 mL Internal Label

    100 mL Internal Label

    100 mL External Label

    100 mL External Label

    100 mL Carton Label

    100 mL Carton Label
  • INGREDIENTS AND APPEARANCE
    VUEWAY 
    gadopiclenol injection
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 0270-7015
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GADOPICLENOL (UNII: S276568KOY) (Gadopiclenol - UNII:S276568KOY) GADOPICLENOL485.1 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    TETRAXETAN (UNII: 1HTE449DGZ)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    TROMETHAMINE (UNII: 023C2WHX2V)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 0270-7015-4625 in 1 CASE09/21/2022
    130 mL in 1 VIAL, SINGLE-DOSE; Type 0: Not a Combination Product
    2NDC: 0270-7015-4825 in 1 CASE09/21/2022
    250 mL in 1 VIAL, SINGLE-DOSE; Type 0: Not a Combination Product
    3NDC: 0270-7015-646 in 1 CASE09/21/2022
    31 in 1 CARTON
    3100 mL in 1 VIAL, SINGLE-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA21698609/21/2022
    VUEWAY 
    gadopiclenol injection
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 0270-7020
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GADOPICLENOL (UNII: S276568KOY) (Gadopiclenol - UNII:S276568KOY) GADOPICLENOL485.1 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    TETRAXETAN (UNII: 1HTE449DGZ)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    TROMETHAMINE (UNII: 023C2WHX2V)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 0270-7020-3810 in 1 CASE09/21/2022
    13 mL in 1 VIAL, SINGLE-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA21698609/21/2022
    VUEWAY 
    gadopiclenol injection
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 0270-7025
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GADOPICLENOL (UNII: S276568KOY) (Gadopiclenol - UNII:S276568KOY) GADOPICLENOL485.1 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    TETRAXETAN (UNII: 1HTE449DGZ)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    TROMETHAMINE (UNII: 023C2WHX2V)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 0270-7025-4010 in 1 CASE09/21/2022
    17.5 mL in 1 VIAL, SINGLE-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA21698609/21/2022
    VUEWAY 
    gadopiclenol injection
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 0270-7030
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GADOPICLENOL (UNII: S276568KOY) (Gadopiclenol - UNII:S276568KOY) GADOPICLENOL485.1 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    TETRAXETAN (UNII: 1HTE449DGZ)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    TROMETHAMINE (UNII: 023C2WHX2V)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 0270-7030-4210 in 1 CASE09/21/2022
    110 mL in 1 VIAL, SINGLE-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA21698609/21/2022
    VUEWAY 
    gadopiclenol injection
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 0270-7035
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GADOPICLENOL (UNII: S276568KOY) (Gadopiclenol - UNII:S276568KOY) GADOPICLENOL485.1 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    TETRAXETAN (UNII: 1HTE449DGZ)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    TROMETHAMINE (UNII: 023C2WHX2V)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 0270-7035-4410 in 1 CASE09/21/2022
    115 mL in 1 VIAL, SINGLE-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA21698609/21/2022
    Labeler - BRACCO DIAGNOSTICS INC (849234661)
    Registrant - BRACCO DIAGNOSTICS INC (849234661)
    Establishment
    NameAddressID/FEIBusiness Operations
    Liebel-Flarsheim Company LLC109024984LABEL(0270-7030, 0270-7025, 0270-7020, 0270-7035, 0270-7015) , MANUFACTURE(0270-7020, 0270-7025, 0270-7015, 0270-7030, 0270-7035) , PACK(0270-7025, 0270-7035, 0270-7020, 0270-7030, 0270-7015)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guerbet503171949ANALYSIS(0270-7020, 0270-7025, 0270-7035, 0270-7015, 0270-7030) , API MANUFACTURE(0270-7015, 0270-7030, 0270-7035, 0270-7025, 0270-7020)

    • Trademark Results [Vueway]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    VUEWAY
    VUEWAY
    97222742 not registered Live/Pending
    BRACCO IMAGING S.p.A.
    2022-01-17
    © 2024 FDA.report
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