Brand Name

Fotivda

Generic Name
Tivozanib
View Brand Information
FDA approval date: March 10, 2021
Classification: Kinase Inhibitor
Form: Capsule

What is Fotivda (Tivozanib)?

FOTIVDA is indicated for the treatment of adult patients with relapsed or refractory advanced renal cell carcinoma following two or more prior systemic therapies. FOTIVDA is a kinase inhibitor indicated for the treatment of adult patients with relapsed or refractory advanced renal cell carcinoma following two or more prior systemic therapies.
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Related Clinical Trials

Phase 2 Study of Combination Tivozanib and Nivolumab in Advanced Non-Clear Cell Renal Cell Carcinoma

Summary: To learn if giving tivozanib in combination with nivolumab can help to control advanced nccRCC.

Short TeRm Intensified Pembrolizumab (KEytruda) and Tivozanib for High-Risk Renal Cell Carcinoma - STRIKE

Summary: This phase III trial compares the effect of adding tivozanib to standard therapy pembrolizumab versus pembrolizumab alone for the treatment of patients with high-risk renal cell carcinoma (RCC). Immunotherapy with monoclonal antibodies, such as pembrolizumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Tivozanib is in a...

Phase II Study Evaluating Efficacy of Tivozanib (AV-951) in Biliary Tract Cancers

Background: Cholangiocarcinoma (CCA) is an aggressive cancer of the bile ducts. People with CCA have few treatment options and poor survival. Researchers want to see if a new drug can stop or slow CCA growth.