Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
PAT101 is a recombinant human albumin (rHA)-conjugated urate oxidase variant being developed by ProAbTech for the treatment of gout and other metabolic conditions. The drug is produced using ProAbTech's proprietary SelecAll™ and Albubody™ platforms, which facilitate the site-specific conjugation of recombinant human albumin to an *Aspergillus flavus* urate oxidase (AfUox) through a clickable non-natural amino acid (frTet) and an Inverse electron demand Diels–Alder (IEDDA) reaction. This albumin-conjugation strategy is designed to extend the therapeutic half-life and reduce the immunogenicity typically associated with PEGylated urate oxidase treatments like pegloticase. Preclinical data in transgenic mice demonstrated that PAT101 has a half-life more than double that of pegloticase. It is currently in Phase 1 clinical development for gout, congenital disorders, and endocrinology/metabolic conditions.
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 PAT101.