CERo Therapeutics, Inc. Receives FDA Clearance of Investigational New Drug Application to Initiate Phase 1 Clinical Trial of Its Lead Compound CER-1236 in Acute Myelogenous Leukemia
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CERo Therapeutics Holdings, Inc. has received FDA clearance to initiate Phase 1 clinical trials for its lead compound, CER-1236, targeting acute myelogenous leukemia. This marks a significant step for the company in advancing its immunotherapy treatments.
November 15, 2024 | 2:00 pm
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CERo Therapeutics has received FDA clearance to begin Phase 1 trials for CER-1236, a treatment for acute myelogenous leukemia. This regulatory approval is a crucial step in the company's development pipeline.
The FDA clearance for CER-1236's Phase 1 trial is a positive regulatory development, likely boosting investor confidence and potentially increasing the stock price. This approval is a key milestone in CERo's product development, indicating progress in their pipeline.
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