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Cullinan Therapeutics doses first patient in registrational Phase 2 CLN-049 study for acute myeloid leukemia

Cullinan Therapeutics doses first patient in registrational Phase 2 CLN-049 study for acute myeloid leukemia
Cullinan starts Phase 2 CLN-049 trial

Cullinan Therapeutics has begun dosing patients in its planned registrational Phase 2 study evaluating CLN-049, an investigational FLT3 T cell engager, in adults with relapsed or refractory acute myeloid leukemia.

The first patient has now received the treatment, marking a significant step in the clinical development of CLN-049. The study aims to assess the efficacy and safety of this therapeutic approach for individuals living with difficult-to-treat AML. This milestone reflects Cullinan Therapeutics’ commitment to advancing therapies for hematologic malignancies.

Cullinan Therapeutics previously presented data from its Phase 3 REZILIENT3 trial at WCLC26, with additional details discussed in an investor webcast, according to company reports. The REZILIENT3 study evaluated zipalertinib in combination with chemotherapy. Cullinan also announced plans for a September webcast to review these Phase 3 results.

This material may contain third-party opinions, none of the data and information on this webpage constitutes investment advice according to our Disclaimer. While we adhere to strict Editorial Integrity, this post may contain references to products from our partners.

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