The Front Room — a clinical regulatory commons
RSS
← Back to feed

Inqovi plus venetoclax cleared for AML ineligible for intensive chemo

Sponsor
Taiho Oncology, Inc.
Drug
Inqovi · decitabine/cedazuridine
Indication
acute myeloid leukemia ineligible for intensive induction chemotherapy
More on Taiho Oncology, Inc. Google News

FDA approved Inqovi (decitabine/cedazuridine) plus venetoclax for acute myeloid leukemia patients ineligible for intensive induction chemotherapy.

What this means

Inqovi is a combination pill that contains two drugs: decitabine, which interferes with cancer cell growth, and cedazuridine, which helps decitabine stay active in the body longer. Today FDA approved Inqovi to be used alongside venetoclax for adults with acute myeloid leukemia who cannot tolerate intensive chemotherapy. This approval gives these patients a new treatment option that may help manage their cancer with a less intensive approach.

Read original at accessdata.fda.gov
Topic AML