Clinical trials
Full profile accessFollow clinical development from trial design and recruitment through results.
- Trial phase
- Status
- Readouts
Company intelligence / Profile preview
Bezoloven, Inc. was a virtual biotechnology company founded in 2007 to develop a reformulated, grape-flavored version of d-penicillamine for the treatment of low-level lead poisoning in children. Established by angel investor Roger Kitterman in collaboration with Dr. Michael Shannon of Children's Hospital Boston, the company aimed to address a significant gap in pediatric toxicology by providing a more palatable and effective chelation therapy. The company operated as a shell entity to fund specific clinical trials in partnership with Tedor Pharma, a contract development and manufacturing organization. Its lead program reached Phase 2 clinical testing before the trial was ultimately withdrawn. Following the withdrawal of its clinical program and the passing of its scientific lead, the company is no longer active in drug development.
Beyond the preview
Explore clinical development, deal activity, and the competitive landscape with Gosset’s full data platform.
Follow clinical development from trial design and recruitment through results.
Explore licensing agreements, acquisitions, and the assets behind each deal.
Trace financing activity and the investors behind a company’s development.
Compare peer pipelines by target, modality, and therapeutic area.
Explore technology platforms and the patent landscape around relevant assets.
Connect company news and source material to the questions you’re investigating.
See how Gosset can support your research on Bezoloven.