drugset / Trial / NCT01386099

A PK-PD Study of PSN821 in Type 2 Diabetes Patients (T2DM)

NCT01386099 ↗

Phase 2 Completed 66 enrolled Prosidion Ltd.
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to investigate the pharmacokinetics and pharmacodynamics of PSN821 in patients with type 2 diabetes. Subjects will be assessed for beta-cell function using a hyperglycaemic clamp before the start of treatment and at the end of a 12 week treatment period as the primary endpoint. HbA1c, fasting plasma glucose and body weight are secondary endpoints.

Timeline

Start
2011-05
Primary completion
2012-01
Completion
2012-05

Drugs

EvaluationDrugModalityDoseRoute
Subject PSN821 Unknown 75 mg —
Subject PSN821 Unknown 250 mg —
Subject PSN821 Unknown 625 mg —