Faster gene‑edited CAR T cell production for blood cancers

CORE C Technology Implementation/Development and Correlative Sciences

NIH-funded research University of Pennsylvania · NIH-11192836

Making safer, faster gene‑edited CAR T cell treatments for people with relapsed or hard‑to‑treat blood cancers like AML and other lymphoid malignancies.

Quick facts

Grant typeP01 program project
Study typeNIH-funded research
Funding institutionUniversity of Pennsylvania NIH-funded
Lab location1 site (Philadelphia, United States)
Project IDNIH-11192836 on NIH RePORTER

What this research studies

At the University of Pennsylvania, two lab cores will work together to shorten and standardize how gene‑edited CAR T cells are made so treatments can be produced more quickly and consistently. They will use CRISPR and base‑editing methods to modify T cells (for example, removing CD5 or editing CD45) and will also edit matching blood stem cells when needed. The team will develop and run safety and product‑release tests that meet FDA expectations and support three linked clinical trials. These efforts are meant to improve manufacturing, safety testing, and the ability to move edited cell therapies into patient treatment.

Who could benefit from this research

Good fit: Adults with relapsed or refractory acute myeloid leukemia or relapsed lymphoid malignancies who meet eligibility for CAR T or gene‑edited cell therapy trials and can receive care at the trial site.

Not a fit: People without blood cancers, those who are medically ineligible for intensive cell therapies, or those who cannot travel to the trial center are unlikely to benefit directly from this grant's clinical activities.

Why it matters

Potential benefit: If successful, this could speed up access to personalized CAR T therapies and improve safety and durability for patients with AML and other resistant blood cancers.

How similar studies have performed: Standard CAR T therapies have shown clear benefit in some lymphoid cancers, but CRISPR/base‑edited CAR T approaches and CD45/CD5 edits remain experimental and are only beginning to be tested in patients.

Where this research is happening

Philadelphia, United States

Researchers

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page below.
Last reviewed 2026-06-13 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.