Rigel Announces Poster Presentations at the 2025 ASCO Annual Meeting and EHA2025 Congress
- Rigel Pharmaceuticals announced seven poster presentations at the 2025 ASCO Annual Meeting and EHA2025 Congress focusing on GAVRETO and REZLIDHIA data.
- These presentations follow clinical trials that evaluated GAVRETO for RET fusion-positive NSCLC and other tumors, and REZLIDHIA for relapsed/refractory mIDH1 AML patients.
- GAVRETO showed a 70.3% overall response rate with a median duration of response of 19.1 months, while REZLIDHIA demonstrated activity including a 50% ORR and manageable safety profiles.
- In clinical trials of REZLIDHIA in relapsed or refractory AML patients, 16% experienced differentiation syndrome, which was fatal in 1% of cases, while hepatotoxicity was reported in 23% of patients and typically resolved within approximately 12 days.
- These results support REZLIDHIA’s potential benefit in earlier treatment lines for AML and reaffirm GAVRETO's durable efficacy in RET fusion-positive cancers amid manageable risks.
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Rigel Announces Poster Presentations at the 2025 ASCO Annual Meeting and EHA2025 Congress
Final data from the GAVRETO® (pralsetinib) Phase 1/2 ARROW study in RET fusion-positive NSCLC and other solid tumors Supportive data for REZLIDHIA® (olutasidenib) utilization in patients with mIDH1 R/R AML
·Billings, United States
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