Frank Vinluan / medcitynews - GSK drug Jideytro received FDA approval for treating advanced cases of non-small cell lung cancer driven by ROS1 alterations. This molecule came from Nuvalent, which GSK recently acquired for $10.6 billion. The post $10B M&A Deal Pays Off With GSK’s First…
AI Summary: GSK has won FDA approval for its first lung cancer drug, a gene-targeting therapy that validates the company’s heavy investment and recent M&A strategy. The approval follows pivotal trial evidence of clinical benefit and positions GSK competitively in thoracic oncology, offering a new therapeutic choice for patients with the relevant molecular profile.
FDA approves Replimune’s Tudriqev after repeated rejections / 4 wks
FDA clears pivekimab sunirine (Decnupaz) as first BPDCN ADC / 3 months
FDA to revisit Atara/Pierre Fabre cell therapy approval for rare lymphoma / 3 months
FDA advisory panel rejects camizestrant after SERENA‑6 results / 4 months
Decade-Long Persistence of CD19 CAR‑T Cells in B‑Cell Lymphomas / 23 days
Bristol Myers Squibb wins first-in-class approval for protein‑degrader myeloma therapy / 24 days
Belzutifan plus pembrolizumab gains approval for adjuvant RCC / 6 wks
StackHealth RSS


StackHealth Time Machine
NorthFeed Inc. Terms and Conditions / Privacy Policy
Disclaimer: The information provided on this website is intended for general informational purposes only. While we strive for accuracy, we do not guarantee the completeness or reliability of the content. Users are encouraged to verify all details independently. We accept no liability for errors, omissions, or any decisions made based on this information.