GSK reports 94% response rate for Jideytro in ROS1-positive lung cancer at World Conference
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GSK is moving a newly acquired lung-cancer drug, Jideytro, toward FDA review after presenting data at the World Conference on Lung Cancer.
The conference data showed a 94% response rate when Jideytro was used as first-line therapy for patients whose tumors carry the ROS1 alteration.
The results were highlighted as a strong signal for the drug's efficacy in this molecularly defined subset of non-small cell lung cancer, supporting GSK's plan to expand the indication.
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This writeup was produced by pharmadog from original reporting by Endpoints.
Original headline: “GSK heads to FDA with recently acquired drug from Nuvalent”
read at Endpoints ↗85 words · retrieved Sep 14
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