Taiho Oncology makes Inqovi, the oral decitabine-cedazuridine that in May 2026 became the first all-oral hypomethylating backbone for venetoclax in AML.
Taiho Oncology, the US arm of Otsuka's Taiho based in Princeton and Tokyo, makes Inqovi, the oral decitabine and cedazuridine combination that in May 2026 became the first all-oral hypomethylating backbone for venetoclax in acute myeloid leukaemia. Cedazuridine is a cytidine deaminase inhibitor that makes oral decitabine bioavailable; Inqovi was approved for myelodysplastic syndromes and chronic myelomonocytic leukaemia in 2020 and, on 13 May 2026, with venetoclax for newly diagnosed AML in adults unfit for intensive induction on the ASCERTAIN-V trial, and the company also markets Lonsurf and futibatinib. OnCo links it to acute myeloid leukaemia and to the oral decitabine drug record. Whether an all-oral regimen changes where and how older patients with AML are treated is the open question. The FDA approval notice is linked.
Oral decitabine-cedazuridine is a pill version of the hypomethylating chemotherapy that, since May 2026, lets older AML patients take their whole venetoclax regimen at home.
Zipalertinib is an experimental small-molecule drug from Taiho Oncology in phase 3 trials for non-small-cell lung cancer, aimed at EGFR.
Shares Decitabine + cedazuridine (oral), Acute myeloid leukaemia.
Shares Decitabine + cedazuridine (oral), Acute myeloid leukaemia.
Shares Decitabine + cedazuridine (oral), Acute myeloid leukaemia.
Shares Decitabine + cedazuridine (oral), Acute myeloid leukaemia.