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Taranabant

Alternative Names: taranabant, mk0364, mk-0634
Latest Update: 2024-05-06
Latest Update Note: PubMed Publication

Product Description

Mechanisms of Action: CB1 Agonist

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Merck
Company Location: KENILWORTH NJ 07033
Company CEO: Robert M. Davis
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Taranabant

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Phase 3: Obesity|Overweight|Type 2 Diabetes

Phase 2: Urinary Incontinence|Overactive Bladder|Obesity|Tobacco Use Disorder

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Taranabant: 1-Yr Weight Loss Followed by 1-Yr Prevention of Weight Regain with 1-Year Extension

P3

Terminated

Obesity

2008-10-02

A Weight Maintenance Study of MK-0364 PN012 with 1-year Extension

P3

Terminated

Obesity

2008-10-02

NCT00131391

P3

Terminated

Obesity

2008-02-01

NCT00420589

P3

Terminated

Obesity

2008-02-01

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