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An Eighteen Month Efficacy and Safety Study in Obese Patients (0364-020)(COMPLETED)

Merck Sharp & Dohme (MSD) logo

Merck Sharp & Dohme (MSD)

Status and phase

Completed
Phase 3
Phase 2

Conditions

Obesity and Obesity-related Medical Conditions

Treatments

Drug: taranabant

Study type

Interventional

Funder types

Industry

Identifiers

NCT00131430
2005_044
0364-020
MK-0364-020

Details and patient eligibility

About

A study to determine the safety and efficacy of an investigational drug in patients with obesity.

Enrollment

500 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Obese patients with a body mass index between 30kg/m2 and 43 kg/m2, inclusive (BMI between 27 kg/m2 and 43kg/m2, inclusive for those with obesity-related comorbidities including hypertension, dyslipidemia and sleep apnea).

Exclusion criteria

  • Patients with serious or unstable current or past medical conditions.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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