Poxel SA announced positive results from the single ascending dose stage, which is the first stage of the ongoing PXL770 Phase 1 clinical trial. PXL770 is a first-in-class direct adenosine monophosphate-activated protein kinase (AMPK) activator, a key enzyme in energy metabolism acting as an energy sensor regulating glucose and lipid levels. AMPK activation is considered to mimic the effects of long-term exercise and plays an important role in diabetes management, especially for patients with cardiovascular risk factors.
In the first part of the study, safety, tolerability and pharmacokinetics of six single ascending oral doses of PXL770 were assessed in 64 healthy male subjects. Overall, the results indicate that PXL770 exhibits a favorable safety and tolerability profile with no serious adverse events reported nor safety signals. Pharmacokinetic assessment showed that PXL770 plasma exposure (Cmax and AUC) increased in a dose dependent manner following oral administration with moderate inter-individual variability. The second part of the trial is on track and will assess safety, tolerability, pharmacokinetics and target engagement of multiple ascending doses.
“Poxel continues to solidify its leadership position in the type 2 diabetes therapeutic area with two programs successfully advancing in clinical development. We are very pleased with the first clinical results and look forward to continuing to move this program forward as well as Imeglimin, which is in late stage clinical development,” said Thomas Kuhn, CEO of Poxel. “PXL770 is a first-in-class product with a unique mode of action which we believe targets an important mechanism for the treatment of type 2 diabetes as well as other metabolic disorders.”
Poxel presented the first preclinical data on PXL770 at the World Congress on Insulin Resistance, Diabetes and Cardiovascular Diseases in Los Angeles last November, demonstrating that PXL770 significantly improves glucose tolerance, lipid profile as well as liver weight in a type 2 diabetes mouse model. Together, the results highlight the potential of PXL770 as a novel oral agent for the treatment of type 2 diabetic patients with added benefits on lipid abnormalities.
