amivantamab-vmjw injection
for intravenous use Initial U.S. Approval: 2021
Rybrevant (amivantamab-vmjw) is a prescription medicine used to treat adults with locally advanced or metastatic non-small cell lung cancer (NSCLC) that have EGFR exon 20 insertion mutations.
Facts about amivantamab-vmjw injection
Disease Indications-Lung Cancer
Manufacturer-Janssen Biotech
Usage-Intravenous
Medicine Approved By-European Medical Agency (EMA), 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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Query For amivantamab-vmjw injection
Approved accessible "amivantamab-vmjw injection"
Amivantamab is indicated for the treatment of adults with locally advanced or metastatic non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) exon 20 insertion mutations, as detected by an FDA-approved test, whose disease has progressed on or after platinum-based chemotherapy.
Amivantamab, sold under the brand name Rybrevant, is a bispecific monoclonal antibody used to treat non-small cell lung cancer. Amivantamab is a bispecific epidermal growth factor (EGF) receptor-directed and mesenchymal–epithelial transition (MET) receptor-directed antibody. It is the first treatment for adults with non-small cell lung cancer whose tumors have specific types of genetic mutations: epidermal growth factor receptor (EGFR) exon 20 insertion mutations. The most common side effects include rash, infusion-related reactions, skin infections around the fingernails or toenails, muscle and joint pain, shortness of breath, nausea, fatigue, swelling in the lower legs or hands or face, sores in the mouth, cough, constipation, vomiting and changes in certain blood tests.
Amivantamab was approved for medical use in the United States in May 2021, and in the European Union in December 2021. The U.S. Food and Drug Administration considers it to be a first-in-class medication.
How can 1 go about obtaining amivantamab-vmjw injection?
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Rybrevant (amivantamab-vmjw injection) for intravenous use Initial U.S. Approval: 2021
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