Daraxonrasib shows 35% response rate in second‑line RAS‑mutated pancreatic cancer
Phase 1/2 data from a monotherapy study of daraxonrasib in patients with RAS G12‑mutated pancreatic ductal adenocarcinoma reported an objective response rate of 35% when used as a second‑line treatment.
The trial also observed response rates of 29% in patients with any RAS mutation receiving second‑line therapy and 20% in those treated in the third‑line setting or later. Safety findings indicated that 96% of participants experienced treatment‑related adverse events, most of which were low‑grade gastrointestinal or skin issues, and no treatment‑related deaths occurred.
Daraxonrasib is now advancing into three phase 3 programs, including the global RASolute 303 trial that will compare the drug with standard‑of‑care chemotherapy in the second‑line setting.
This writeup was produced by pharmadog from original reporting by onclive.
Original headline: “Daraxonrasib Monotherapy Elicits Meaningful Responses in Previously Treated, RAS-Mutated Pancreatic Cancer”
read at onclive ↗
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