Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
UB-VV400 + rapamycin is an investigational **combination therapy** comprising UB-VV400, an in vivo CD22-directed CAR-T cell therapy, and rapamycin, an oral mTOR inhibitor. UB-VV400 is engineered to target CD22, a clinically validated B-cell antigen expressed in most B-cell malignancies, and incorporates a synthetic cytokine system (RACR2) to enhance CAR-T cell survival and potency. Rapamycin (also known as sirolimus) is used for its antiproliferative and immunomodulatory properties; it inhibits the mammalian target of rapamycin (mTOR) pathway, modulating cellular growth, proliferation, and survival. The combination is intended to address relapsed or refractory large B-cell lymphomas (LBCL), including DLBCL, high-grade lymphoma, follicular lymphoma Grade 3B, and primary mediastinal B-cell lymphoma, particularly in populations exposed to prior CD19-directed CAR-T therapy or those who are CAR-T naive. It is in early-stage clinical development focusing on safety, pharmacokinetics, and efficacy optimization[1][3][4][5].
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 UB-VV400 + rapamycin.