Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
XCE853 is a first-in-class, synthetic small molecule inhibitor of protein disulfide isomerase (PDI), an enzyme involved in cancer cell metabolism and survival. Developed by Oregon Therapeutics and co-developed with Lantern Pharma, XCE853 selectively induces autophagy in cancer cells by inhibiting PDI, a target highly expressed in various tumor types and associated with drug resistance. Preclinical studies have demonstrated robust antitumor activity across multiple cancer models—including ovarian, pancreatic, prostate, colorectal, non-small cell lung cancers (NSCLC), renal cell carcinoma (RCC), breast cancer, head and neck cancers, leukemia—and particularly against tumors resistant to current chemotherapies. The drug is orally bioavailable and has shown efficacy at low nanomolar concentrations in vitro as well as significant tumor growth inhibition in vivo xenograft models. The primary development focus is on drug-resistant ovarian and advanced pancreatic cancers; additional potential indications include liver cancer and several orphan or pediatric CNS cancers[1][2][4][5][6][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 XCE853.