Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
JMT601 is a first-in-class bispecific fusion protein designed for the treatment of relapsed or refractory CD20-positive B-cell non-Hodgkin lymphoma, including diffuse large B-cell lymphoma. It combines an anti-CD20 antibody with a signal regulatory protein alpha (SIRPα) fragment that binds to CD47. By simultaneously targeting CD20 and blocking the "don't eat me" signal mediated by CD47, JMT601 enhances both antibody-dependent cell-mediated cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC), promoting immune-mediated elimination of malignant B cells. The drug is administered intravenously and is currently in Phase 1/2 clinical trials. It has been granted Fast Track Designation by the U.S. FDA for diffuse large B-cell lymphoma[2][3][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 JMT601.