esmo - Evidence for efficacy is based on the findings from the ROSELLA study
AI Summary: The FDA granted marketing authorization for relacorilant in combination with nab‑paclitaxel to treat platinum‑resistant epithelial ovarian, fallopian tube and primary peritoneal cancers. Regulators cited clinical benefit in a difficult‑to‑treat population, providing an additional therapeutic option for patients with limited choices and marking an important regulatory milestone.
VOLGA Phase III shows survival benefit for bladder cancer neoadjuvant combo / 15 days
Datroway secures regulatory approvals in breast cancer across US and EU / 8 days
FDA clears first targeted therapy for ultra-rare NRG1-driven cholangiocarcinoma / 20 days
FDA grants early access to experimental pancreatic cancer drug / 29 days
FDA flags misleading cancer drug claims tied to biotech billionaire / 2 months
FDA clears pivekimab sunirine (Decnupaz) as first BPDCN ADC / 46 hrs
FDA to revisit Atara/Pierre Fabre cell therapy approval for rare lymphoma / 22 days
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