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Cullinan Therapeutics advances CLN-049 to Phase 2 after positive FDA feedback

Cullinan Therapeutics advances CLN-049 to Phase 2 after positive FDA feedback
Cullinan moves CLN-049 to Phase 2

Cullinan Therapeutics announced it has received positive feedback from the U.S. Food and Drug Administration following an End-of-Phase 1 meeting for its investigational therapy CLN-049.

The company now plans to move its FLT3xCD3 T cell engager into a potentially registrational Phase 2 trial targeting patients with relapsed or refractory acute myeloid leukemia (AML). Cullinan Therapeutics aims to address a significant unmet need in AML treatment by advancing this next phase of clinical development.

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