Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
ASD-49 is a novel selenium-containing hybrid molecule derived from aspirin, specifically incorporating a selenocyanate moiety. Developed by researchers at the Penn State University College of Medicine, it was designed to enhance the anticancer properties of non-steroidal anti-inflammatory drugs (NSAIDs) by leveraging the redox-active and chemopreventive properties of selenium. In preclinical studies, ASD-49 demonstrated significant cytotoxicity against various cancer cell lines, including colon (HCT116) and pancreatic (MiaPaCa-2) cancer, with IC50 values in the low micromolar range (1.0 μM and 2.5 μM, respectively). Its mechanism of action involves the induction of apoptosis, characterized by caspase activation and subsequent PARP cleavage, showing markedly higher potency compared to parent aspirin.
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 ASD-49.