Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**PSB202** is an investigational, fixed-combination B-cell–depleting biologic developed by Qilu Pharmaceutical and Qilu Puget Sound Biotherapeutics. It is manufactured as a single product containing a 1:1 molecular ratio of two engineered, afucosylated humanized IgG1 monoclonal antibodies: PSB102, an Fc-enhanced type II anti-CD20 antibody, and PSB107, an anti-CD37 antibody. By co-targeting CD20 and CD37 on malignant and normal B cells, PSB202 induces direct target-mediated B-cell killing and promotes Fcγ receptor-mediated antibody-dependent cellular cytotoxicity and complement-dependent cytotoxicity. It is in Phase 1 clinical development for previously treated relapsed or refractory CD20-positive indolent B-cell malignancies, including follicular lymphoma, chronic lymphocytic leukemia, small lymphocytic lymphoma, marginal zone lymphoma, mucosa-associated lymphoid tissue lymphoma, mantle cell lymphoma, and Waldenström macroglobulinemia.
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 PSB202 (Qilu Pharmaceutical).