drugset / Trial / NCT01196728

Single-centre, Randomised, Double-blind, Placebo-controlled, Four-way Crossover Clinical Study to Investigate Safety and Tolerability and Pharmacokinetics of Single Doses of CM3.1-AC100 in Patients With Type 2 Diabetes

NCT01196728 ↗

Phase 1 Completed 16 enrolled CellMed AG, a subsidiary of BTG plc.
RandomizedCrossoverTriple-blindBasic science

Summary

The primary objective of this study is to assess the safety and tolerability of the Glucagon-like peptide-1 (GLP-1) peptide analogue CM3.1-AC100 after single subcutaneous (sc) doses in patients with T2DM.

Timeline

Start
2010-09
Primary completion
2010-11
Completion
2010-11

Drugs

EvaluationDrugModalityDoseRoute
Subject CM3.1-AC100 Peptide — Subcutaneous