Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
YL217 is a next-generation antibody-drug conjugate (ADC) developed by Suzhou Medilink Therapeutics. It specifically targets cadherin-17 protein (CDH17), which is overexpressed in several gastrointestinal cancers, including gastric cancer, colorectal cancer, pancreatic cancer, and hepatocellular carcinoma. The ADC consists of three components: a recombinant humanized IgG1 monoclonal antibody targeting CDH17 (YL217-mAb), a topoisomerase I inhibitor payload (YL0010014), and an enzymatically cleavable methylsulfonyl pyrimidine tripeptide linker. Preclinical studies have shown that YL217 effectively suppresses tumor growth in models of human colorectal and gastric cancers. The drug is currently in Phase 1 clinical trials for advanced solid tumors with a focus on gastrointestinal neoplasms.
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 YL217.