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Revolution Medicines’ experimental RAS(ON) inhibitor daraxonrasib has shown substantial survival benefits in advanced pancreatic cancer and has been cleared for expanded access by the U.S. Food and Drug Administration.
Peer‑reviewed phase I/II data published in the New England Journal of Medicine involving 168 previously treated patients reported response rates up to 35% at the 300 mg dose, median progression‑free survival around 8–8.5 months and overall survival in the 13–15.6 month range in selected cohorts.
An ongoing global phase III trial (RASolute 302) produced topline results showing median overall survival roughly 13.2 months versus 6.7 months with chemotherapy, and the company reported a ~60% reduction in risk of death in the intent‑to‑treat population.
Safety signals include treatment‑related adverse events in about 96% of patients and grade ≥3 events in ~30%, most commonly rash, stomatitis, nausea and diarrhea; most events were manageable with dose modification and supportive care.
Revolution plans regulatory filings, expanded registrational trials across pancreatic and lung cancer indications, and has reported increased clinical spending amid strong demand for expanded access.
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The trial targeted previously treated (second-line) PDAC patients and tested daraxonrasib as monotherapy versus standard chemo. Given PDAC’s high KRAS mutation rate and the reported survival gains, the drug could quickly shift treatment practice if regulators confirm results; rash management will be important for quality of life.


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