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Last Updated: October 16, 2019

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CLINICAL TRIALS PROFILE FOR PHENTERMINE HYDROCHLORIDE

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Clinical Trials for Phentermine Hydrochloride

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00000506 Cardiovascular System in Obesity: Effect of Treatment Completed National Heart, Lung, and Blood Institute (NHLBI) Phase 2 1983-05-01 To determine the long-term efficacy of the combination therapy of phentermine and fenfluramine in conjunction with diet, exercise, and behavior modification in the treatment of simple, moderate obesity.
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 Completed AstraZeneca Phase 2 2006-11-01 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.
NCT00518466 Pharmacokinetic Comparison of Multiple Formulations of Topiramate and Phentermine in Obese Adults Completed VIVUS, Inc. Phase 1 2007-07-01 The primary objective of this study is to describe the single- and multiple-dose pharmacokinetic profiles of two novel formulations of topiramate and commercially available immediate release topiramate, all dosed with immediate release phentermine.
NCT00563368 A Study Comparing Multiple Doses of VI-0521 With Placebo and Their Single-agent Constituents for Treatment of Obesity in Adults Completed Medpace, Inc. Phase 3 2007-12-01 The objective of this study is to evaluate the safety and efficacy of various doses of VI-0521 compared to both placebo, and the single-agent components that comprise each combination dose. This study will provide confirmatory data to demonstrate that doses of VI-0521 have efficacy that is greater than placebo and each of the single-agent components that comprise the combination dose.
NCT00563368 A Study Comparing Multiple Doses of VI-0521 With Placebo and Their Single-agent Constituents for Treatment of Obesity in Adults Completed VIVUS, Inc. Phase 3 2007-12-01 The objective of this study is to evaluate the safety and efficacy of various doses of VI-0521 compared to both placebo, and the single-agent components that comprise each combination dose. This study will provide confirmatory data to demonstrate that doses of VI-0521 have efficacy that is greater than placebo and each of the single-agent components that comprise the combination dose.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for Phentermine Hydrochloride

Condition Name

Condition Name for Phentermine Hydrochloride
Intervention Trials
Obesity 18
Drug Abuse 3
Healthy 2
Binge Eating Disorder 2
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Condition MeSH

Condition MeSH for Phentermine Hydrochloride
Intervention Trials
Obesity 8
Overweight 7
Weight Loss 4
Substance-Related Disorders 3
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Clinical Trial Locations for Phentermine Hydrochloride

Trials by Country

Trials by Country for Phentermine Hydrochloride
Location Trials
United States 68
Mexico 2
Italy 1
Canada 1
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Trials by US State

Trials by US State for Phentermine Hydrochloride
Location Trials
California 9
Texas 5
Florida 5
Arizona 4
Alabama 4
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Clinical Trial Progress for Phentermine Hydrochloride

Clinical Trial Phase

Clinical Trial Phase for Phentermine Hydrochloride
Clinical Trial Phase Trials
Phase 4 7
Phase 3 2
Phase 2 10
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Clinical Trial Status

Clinical Trial Status for Phentermine Hydrochloride
Clinical Trial Phase Trials
Completed 16
Recruiting 7
Not yet recruiting 2
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Clinical Trial Sponsors for Phentermine Hydrochloride

Sponsor Name

Sponsor Name for Phentermine Hydrochloride
Sponsor Trials
VIVUS, Inc. 7
AstraZeneca 4
Lindner Center of HOPE 2
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Sponsor Type

Sponsor Type for Phentermine Hydrochloride
Sponsor Trials
Other 25
Industry 21
NIH 5
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