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Allogene Therapeutics Faces Trial Setback as ALLO-647 Halt Raises Lymphodepletion and Regulatory Timeline Risks

Allogene Therapeutics Faces Trial Setback as ALLO-647 Halt Raises Lymphodepletion and Regulatory Timeline Risks

Allogene Therapeutics (ALLO) has disclosed a new risk, in the Innovation / R&D category.

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Allogene Therapeutics faces uncertainty over whether fludarabine and cyclophosphamide (FC) alone can achieve adequate lymphodepletion to support cema-cel’s efficacy in the ALPHA3 trial, after discontinuation of ALLO-647 due to a Grade 5 SAE. If FC proves insufficient and the study design must be amended to enhance lymphodepletion, the resulting trial delays could impair regulatory timelines and materially weaken the company’s business and financial outlook.

The average ALLO stock price target is $8.71, implying 262.92% upside potential.

To learn more about Allogene Therapeutics’ risk factors, click here.

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