New drug Daraxonrasib nearly doubles survival in pancreatic cancer trial

A new treatment called Daraxonrasib has shown strong results against advanced pancreatic cancer in a recent clinical trial. The drug targets a genetic mutation long considered impossible to treat effectively.

Revolution Medicines presented the Phase 3 trial data on May 31, 2026. The study involved 500 patients with metastatic pancreatic cancer who had already received prior treatment. Daraxonrasib extended median overall survival to 13.2 months compared with 6.7 months on standard chemotherapy. The therapy also lowered the risk of death by 60 percent. Patients reported better quality of life and were less likely to discontinue treatment because of severe side effects. The most frequent adverse events included skin rash in more than 86 percent of participants along with mouth sores, diarrhea, nausea, and vomiting. Daraxonrasib works by binding to cyclophilin A to block the KRAS protein that drives most pancreatic tumors. The company plans to seek regulatory approval from the Food and Drug Administration and other agencies. If approved, the drug could become available to patients within months.

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Scientist in lab studying mouse with DNA and brain inflammation overlays representing Alzheimer’s drug research.
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Experimental drug reduced DNA damage and inflammation in an Alzheimer’s mouse model, King’s College London says

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Scientists at King’s College London report that an experimental compound, KCL-286, repaired markers of DNA damage and lowered brain inflammation in a mouse model of Alzheimer’s disease. The team says the drug—originally developed for spinal cord injury—has already completed Phase 1 safety and tolerability testing in humans, which could speed plans for further clinical studies.

A genetically engineered virus has stopped pancreatic tumors from growing in three patients in an early US clinical trial. The results come from a safety study led by researchers at the University of Minnesota.

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Researchers at Rockefeller University report that a new single-cell screening platform, PerturbFate, can trace how many different genetic disruptions converge on common regulatory programs that drive resistance to the melanoma drug vemurafenib, pointing to potential combination-therapy targets.

A new antibody drug developed by Roche has shown it can clear amyloid from the brain more efficiently than existing treatments while causing far fewer dangerous side effects. The findings on Trontinemab were presented at a major conference in London this month. Researchers say the drug could offer a safer option for people with early-stage Alzheimer’s disease.

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Karolis Schröder, 18, from Heby must take medication every six hours for nephropathic cystinosis. Region Uppsala has denied him the approved long-acting treatment Procysbi due to its cost.

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