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Study of Safety, Tolerability and Efficacy of MK0493 in Obese Patients (0493-008)(COMPLETED)

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00482638
Enrollment
Unknown
Registered
2007-06-05
Start date
2004-05-12
Completion date
2004-10-29
Last updated
2019-11-14

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

Conditions

Obesity

Brief summary

To assess the effect of MK0493 on body weight, blood pressure, mood, and appetite.

Interventions

DRUGMK0493

Sponsors

Merck Sharp & Dohme LLC
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

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

Inclusion criteria

* Patient is between 21 and 65 years * Patient is able to read and understand and complete study questionnaires * Patient is not pregnant or breast-feeding and does not plan to become pregnant for the duration of the study and post-study follow-up period

Exclusion criteria

* Patient has a history of significant psychiatric disorder (such as major depression, bipolar disorder, bulimia, or anorexia nervosa * Patient is HIV positive as determined by medical history * Patient has undergone surgical treatment for obesity * Patient plans to consume more than two 8 ounce glasses of grapefruit juice per day during the study * Patient participated in another clinical study involving an investigational drug) within 3 months prior to Visit 1 * Patient is currently a heavy consumer of alcohol (\>2 drinks per day or \>14 drinks per week \[1 drink is defined as 2 oz hard alcohol, 5 oz wine, 12 oz beer\], or uses (including recreational use) any illicit drugs, or has a history of drug or alcohol abuse

Outcome results

None listed

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