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Efficacy of MK0557 in Combination With Sibutramine or Orlistat (0557-015)(COMPLETED)

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00533481
Enrollment
497
Registered
2007-09-21
Start date
2004-02-29
Completion date
2004-12-31
Last updated
2016-09-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity

Brief summary

Study medicine will be given alone, or in combination with either sibutramine or orlistat, to obese subjects to compare the effect on body weight over a six month period.

Interventions

DRUGMK0557

Sponsors

Merck Sharp & Dohme LLC
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Men and women between the ages of 18-65 who are considered obese (have a body mass index between 30 and 43)

Exclusion criteria

* Subject has high blood pressure or is taking any high blood pressure medicine * History of psychiatric disorder, stroke, or heart disease

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026