esmo - Evidence for efficacy is based on the results from the Study ASTX727-07
AI Summary: The FDA has approved an oral combination (decitabine/cedazuridine plus venetoclax) as a treatment option for newly diagnosed acute myeloid leukemia patients who are older or unfit for intensive therapy. The approval offers an at-home alternative to frequent infusions, potentially reducing clinic visits and improving convenience for a vulnerable population.
VOLGA Phase III shows survival benefit for bladder cancer neoadjuvant combo / 20 days
Datroway secures regulatory approvals in breast cancer across US and EU / 13 days
FDA clears first targeted therapy for ultra-rare NRG1-driven cholangiocarcinoma / 24 days
FDA grants early access to experimental pancreatic cancer drug / 4 wks
FDA approves relacorilant plus nab‑paclitaxel for resistant ovarian cancers / 7 wks
FDA flags misleading cancer drug claims tied to biotech billionaire / 2 months
FDA clears pivekimab sunirine (Decnupaz) as first BPDCN ADC / 6 days
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