Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
PRGN-3006 is a multigenic, autologous chimeric antigen receptor T cell (CAR-T) therapy developed by Precigen for the treatment of hematologic malignancies. It is engineered using a non-viral system to express a CAR targeting CD33, membrane-bound interleukin-15 (mbIL15) to enhance in vivo expansion and persistence of the CAR-T cells, and an inducible kill switch for improved safety. The therapy is designed to selectively target and eliminate CD33-positive tumor cells while allowing for controlled depletion of the CAR-T cells if needed. Its primary indications are relapsed or refractory acute myeloid leukemia (AML) and high-risk myelodysplastic syndromes (MDS). PRGN-3006 has received orphan drug designation and fast track status from the FDA for AML[1][5][7][8].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on PRGN-3006.