Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
WEF-001 is a novel anticancer agent composed of a conjugate between human serum albumin and the cytotoxic payload monomethyl auristatin E (MMAE). It is designed for targeted delivery to tumor cells with KRAS mutations via increased pinocytosis, leveraging cancer cells' propensity to engulf albumin and thereby enhancing intracellular delivery of MMAE. The molecule functions as a tubulin inhibitor, disrupting microtubule formation and resulting in apoptotic cancer cell death. WEF-001 is in clinical trials for advanced solid tumors with KRAS mutations, including pancreatic, colorectal, non-small cell lung cancer, platinum-resistant serous ovarian cancer, cholangiocarcinoma, and urothelial bladder cancer. The drug was originally developed by Syndivia and later spun into Auricula Biosciences, co-founded by TVM Life Science and Lilly[2][5][7][9][10].
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 WEF-001.