Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
ATC161 is an orally bioavailable small molecule Autophagy-Targeting Chimera (AUTOTAC) developed by Autotac Bio for the treatment of Parkinson's disease and other neurodegenerative disorders. It functions by selectively binding to pathological alpha-synuclein aggregates and the autophagy receptor p62 (SQSTM1), thereby facilitating the degradation of these toxic aggregates via the autophagy-lysosomal pathway. Unlike traditional inhibitors, ATC161 promotes the clearance of existing protein aggregates without affecting the physiological monomeric form of alpha-synuclein. Preclinical data indicate that ATC161 reduces neuroinflammation and improves motor performance in animal models. The compound has received Investigational New Drug (IND) approval for Phase 1 clinical trials in South Korea.
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 ATC161.