Rigel Pharmaceuticals (RIGL) announced the first patient has been enrolled in the dose expansion phase of the ongoing Phase 1b study of R2891 in patients with relapsed or refractory lower-risk myelodysplastic syndrome. R289 is Rigel’s potent and selective dual inhibitor of interleukin receptor-associated kinases 1 and 4. Enrollment in the dose escalation phase of the study was completed in July 2025, and the company expects to share updated data from the study later this year.
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