tisotumab vedotin-tftv for injection
for intravenous use Initial U.S. Approval: 2021
Tivdak (tisotumab vedotin-tftv) is a prescription medicine used to treat adults with recurrent or metastatic cervical cancer.
Facts about tisotumab vedotin-tftv for injection
DISEASE INDICATIONS-Gynaecological Cancer, Solid Tumor
MANUFACTURER-Seattle Genetics Genmab
USAGE-For Injection: 40 mg as a lyophilized cake or powder in a single-dose vial for reconstitution.
MEDICINE APPROVED BY-Food and Drug Administration (FDA)
Summary of FDA-approved use on approval date: Click Here
(see Drugs@FDA for complete indication)
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If you have a prescription from a Registered Medical Practitioner (RMP), IPN in Delhi can assist you in obtaining access to genuine medication. Our professional will provide you with a step-by-step guide on how to legally and safely import “sotorasib tablets” based on the information you provide.
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Query For tisotumab vedotin-tftv for injection
Approved accessible "tisotumab vedotin-tftv for injection"
Tisotumab vedotin, sold under the brand name Tivdak, is an antibody-drug conjugate used to treat cervical cancer. It is a combination of tisotumab, a monoclonal antibody against tissue factor, and monomethyl auristatin E (MMAE), a potent inhibitor of cell division. It is administered by infusion into a vein. Tisotumab vedotin was approved for medical use in the United States in September 2021. The U.S. Food and Drug Administration considers it to be a first-in-class medication.
How can 1 go about obtaining tisotumab vedotin-tftv for injection?
If tisotumab vedotin-tftv for injection are not yet approved or available in your area, you may request its price in India under a specific brand name through IPN. For assistance and guidance, you can contact us by providing complete details. Our pharmaceutical expert will help you find a suitable and practical solution to your query. To receive comprehensive support, please call us at +91 9891 296 838 (Mr. Tarun) / +91 9811 747 774 (Mr. Neeraj).
Tivdak (tisotumab vedotin-tftv for injection) for intravenous use Initial U.S. Approval: 2021
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