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CERo Therapeutics Presents Data at Society for [Conference Name]

November 4, 2025 Dr. Jennifer Chen Health

Summary of the CERo Therapeutics Facts:

This text details promising preclinical and clinical advancement of CER-1236, an investigational T cell therapy by CERo Therapeutics ​for treating certain blood cancers. Here’s a breakdown:

Key Highlights:

* CER-1236 & its Mechanism: CER-1236‌ is a T ⁤cell product ⁤engineered to target the TIM-4 ligand. It’s designed to be more durable and resist⁣ exhaustion compared to customary T cell stimulation methods (CD3/CD28). ​ CERo calls these “Chimeric ​Engulfment Receptor T cells”⁤ (“CER-T”) which ​utilize ‍both​ traditional T cell ‌killing and engulfment of cancer cells.
* Preclinical Data: Showed sustained T ⁤cell expansion ⁣and robust cytokine response with CER-1236, unlike the exhaustion seen with​ standard stimulation.⁣ This data was presented at the SITC conference.
* Phase 1 Trial: ‌A first-in-human, multi-center Phase 1/1b study ‍is underway, evaluating CER-1236 in patients with:
* Relapsed/Refractory Acute Myeloid Leukemia⁤ (AML)
* AML in ‌remission with‌ measurable residual disease
​ * Newly diagnosed AML/MDS with TP53 mutations
* trial Focus: The trial is⁣ designed to assess safety (primary outcome) and preliminary efficacy (ORR, CR, cCR, MRD) and pharmacokinetics (PK). it’s currently in the dose escalation phase.
* CERo’s Approach: CERo focuses on engineering⁣ T cells to combine innate and adaptive immunity for more extensive tumor targeting. They believe CER-T cells could be more effective than current CAR-T therapies and possibly ⁢work on both blood cancers and solid tumors.
* CEO Statement: ‌Chris Ehrlich believes the preclinical data supports observations from the ongoing Phase 1 trial.

In essence, CERo is developing a novel T cell therapy​ with‍ a unique mechanism of action, and ‌early data suggests it might ⁢very well be⁢ a promising treatment option for AML and other blood cancers.

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#CER-1236, AML, CERo Therapeutics Holdings, inc., OTC Markets:CERO, Sitc, zero

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