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Inqovi Tablets, FDA Approved for Treatment of MDS and CMML, Available at Biologics by McKesson
Inqovi was approved by the FDA on July 7, 2020, for the treatment of adults with intermediate and high-risk myelodysplastic syndromes (MDS) including chronic myelomonocytic leukemia (CMML).
CARY, N.C., Aug. 24, 2020—Biologics by McKesson, an independent specialty pharmacy specializing in oncology and rare disease areas, has been selected by Taiho Oncology, Inc. as a specialty pharmacy provider for Inqovi (decitabine and cedazuridine) tablets for the treatment of adults with intermediate and high-risk myelodysplastic syndromes (MDS) including chronic myelomonocytic leukemia (CMML), 2 blood malignancies.
Inqovi, approved by the FDA on July 7, 2020, is a fixed-dose oral C-DEC (combination of decitabine and cedazuridine). The FDA granted this therapy orphan drug designation and approved Inqovi through its Priority Review process. By inhibiting cytidine deaminase in the gut and the liver, Inqovi enables the DNA hypomethylating agent, decitabine, to be taken orally for five days to reach systemic exposure levels that match those from five days’ worth of intravenous administration.
Evolving Treatment Paradigms for Hematologic Malignancies in Community Oncology Settings
January 11th 2026In an interview during ASH 2025, Ontada's Ira Zackon, MD explores the role of BTK inhibitors in chronic lymphocytic leukemia treatment, highlighting real-world challenges and emerging therapy strategies.
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