Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
AMG 701 (pavurutamab) is an investigational, half-life extended bispecific T-cell engager (BiTE) antibody designed to target B-cell maturation antigen (BCMA) on multiple myeloma cells and CD3 antigen on T cells. By binding both BCMA and CD3, AMG 701 redirects cytotoxic T lymphocytes to lyse BCMA-expressing tumor cells through T-cell–dependent cellular cytotoxicity. The drug was developed for the treatment of relapsed or refractory multiple myeloma (RRMM), particularly in patients who had received multiple prior lines of therapy. Preclinical studies demonstrated potent anti-myeloma activity, including in patient-derived samples resistant to other therapies, and synergy with immunomodulatory drugs such as lenalidomide and pomalidomide. Clinical trials showed promising response rates; however, development was discontinued for strategic reasons despite encouraging efficacy data[1][2][4][5][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 pavurutamab.