The FDA Has Lifted Clinical Hold On Foghorn Therapeutics' Phase 1 Study Of FHD-286 In Acute Myelogenous Leukemia & Myelodysplastic Syndrome. It Plans To Commence Phase 1 Study Of FHD-286 Plus Decitabine Or Cytarabine In Relapsed/Refractory AML In Q3 2023
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The FDA has lifted the clinical hold on Foghorn Therapeutics' Phase 1 study of FHD-286 in acute myelogenous leukemia and myelodysplastic syndrome. The company plans to commence Phase 1 study of FHD-286 plus decitabine or cytarabine in relapsed/refractory AML in Q3 2023.

June 05, 2023 | 11:12 am
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Foghorn Therapeutics' Phase 1 study of FHD-286 receives FDA approval to proceed, with plans to commence a new study in Q3 2023.
The FDA lifting the clinical hold on Foghorn Therapeutics' Phase 1 study of FHD-286 is a positive development for the company. This allows them to proceed with their research and commence a new study in Q3 2023, which could potentially lead to positive results and increased investor interest in the stock. The news is highly relevant and important for investors in FHTX, and the confidence in the analysis is high due to the direct impact of the FDA's decision on the company's research progress.
CONFIDENCE 90
IMPORTANCE 80
RELEVANCE 100