Clinical trials
Follow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
211At-bisB10-biotin is a novel radiolabeled small molecule conjugate consisting of a bis-closo-decaborate(4-) (bisB10) boron cage structure linked to biotin and radiolabeled with the alpha-emitting radionuclide astatine-211 (211At). Developed by researchers at the University of Washington, Fred Hutch Cancer Center, and the University of Miami, this compound is designed for targeted alpha therapy (TAT) using biotin-streptavidin pretargeting systems. The bisB10 boron cage acts as a dual nucleophilic reagent that intramolecularly traps oxidized astatine, stabilizing the boron-astatine bond and reducing in vivo oxidative deastatination. This design improves pharmacokinetics and reduces off-target toxicity associated with free astatine accumulation in non-target tissues.
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 211At-bisB10-biotin.