drugset / Trial / NCT00402077

A Study to Examine the Safety, Tolerability, and Body Weight Effect of Pramlintide Alone and in Combination With Oral Antiobesity Agents in Overweight and Obese Subjects

NCT00402077

Phase 2 Completed 258 enrolled AstraZeneca
RandomizedParallel-groupSingle-blindTreatment

Summary

This study will examine the safety, tolerability, and body weight effect of subcutaneous pramlintide alone and in various combinations with the oral antiobesity agents sibutramine or phentermine in overweight and obese subjects.

Timeline

Start
2006-11
Primary completion
2007-08
Completion
2007-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Phentermine Small molecule 37.5 mg Oral
Subject Pramlintide Peptide 120 ug Subcutaneous
Subject Sibutramine Small molecule 10 mg Oral

Indications