Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
JMX1122 is a preclinical-stage proteolysis-targeting chimera (PROTAC) protein degrader designed to target and degrade signal transducer and activator of transcription 3 (STAT3). Developed by researchers at the Louisiana State University Health Sciences Center (LSUHSC) and the University of Texas Medical Branch (UTMB), JMX1122 is based on the small-molecule STAT3 inhibitor HJC0152. In preclinical studies, JMX1122 has demonstrated potent antiproliferative and colony-formation inhibitory activities against triple-negative breast cancer (TNBC) and estrogen receptor (ER)-positive breast cancer cell lines. Unlike its parent compound HJC0152, which primarily inhibits STAT3 phosphorylation, JMX1122 induces robust degradation of the total STAT3 protein, leading to apoptosis in breast cancer cells.
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 JMX1122.