Glyscend Therapeutics Announces Publication of GLY-200 First-in-Human Data and Availability of Phase 2a Clinical Results
The data published demonstrate that GLY-200, the company’s lead clinical candidate, mimics the biomarker signature seen with metabolic surgery and appeared to be safe and generally well-tolerated.
- The data published demonstrate that GLY-200, the company’s lead clinical candidate, mimics the biomarker signature seen with metabolic surgery and appeared to be safe and generally well-tolerated.
- Glyscend also presented additional data from its Phase 2a clinical trial of GLY-200 at the recent American Diabetes Association (ADA) 83rd Scientific Sessions, which provide clinical proof-of-concept on its ability to reduce glucose and bodyweight in patients with T2D.
- As highlighted in the publication, safety and pharmacodynamics were assessed in a Phase 1, randomized, double-blind, placebo-controlled, single- and multiple-ascending-dose study in healthy volunteers.
- Data presented at ADA showed that, consistent with the Phase 1 study, no treatment- or dose-related safety signals were observed in the Phase 2a study in patients with T2D.