drugset / Trial / NCT01614782

A Study of the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of MK-5823 in Overweight or Obese Participants Who Are Healthy or Have Type 2 Diabetes Mellitus (MK-5823-002)

NCT01614782 ↗

Phase 1 Terminated 24 enrolled Merck Sharp & Dohme LLC
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to assess the multiple rising dose safety/tolerability and pharmacokinetics of MK-5823 in overweight/obese participants who are healthy and overweight/obese participants with Type 2 diabetes mellitus (T2DM).

Timeline

Start
2012-06
Primary completion
2012-10
Completion
2012-10

Drugs

EvaluationDrugModalityDoseRoute
Subject MK-5823 Unknown 0.35 mg Subcutaneous
Subject MK-5823 Unknown 0.7 mg Subcutaneous
Subject MK-5823 Unknown 1.4 mg Subcutaneous
Subject MK-5823 Unknown 2.8 mg Subcutaneous