Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Systebryl (PTI-110) is a small molecule drug developed by ProteoTech (and later ProtaMed) for the treatment of AL amyloidosis, a rare systemic disease characterized by the accumulation of misfolded protein aggregates. The drug specifically targets and disaggregates insoluble immunoglobulin light chain (AL) amyloid deposits that build up in vital organs such as the heart and kidneys. By breaking down these deposits, Systebryl is intended to facilitate their clearance from the body and restore organ function. Although it received FDA orphan drug designation in January 2015 and was planned for Phase 1/2 clinical trials, development appears to have stalled, and the trademark was abandoned in 2016.
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 Systebryl.