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A 2-Year Study of an Investigational Drug in Obese Patients

2014-08-27 03:54:03 | BioPortfolio

Summary

This is a 2-year study to assess the safety, tolerability, and efficacy of an investigational drug in obese patients.

Study Design

Allocation: Randomized, Control: Placebo Control, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Conditions

Obesity

Intervention

MK0557

Status

Completed

Source

Merck

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-08-27T03:54:03-0400

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