Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
ARC-401 is a proprietary, first-in-class, triple-warhead antibody-drug conjugate (ADC) targeting Nectin-4, developed by Araris Biotech (a subsidiary of Taiho Pharmaceutical). It is designed to treat a broad range of Nectin-4-expressing solid tumors, including triple-negative breast cancer (TNBC) and urothelial carcinoma. ARC-401 is constructed using Araris' proprietary AraLinQ™ site-specific, one-step peptide linker conjugation technology, which allows for payload attachment without prior antibody engineering. The ADC features a drug-to-antibody ratio (DAR) of 6 (2+2+2), delivering three distinct cytotoxic payloads to the same tumor cell: monomethyl auristatin E (MMAE, a tubulin inhibitor) and two different topoisomerase-1 (TOP1) inhibitors (one cell-permeable and one non-cell-permeable). This multi-warhead design is engineered to overcome tumor heterogeneity and cancer resistance while maintaining a highly stable, well-tolerated profile with favorable pharmacokinetics.
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 ARC-401.