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Pexacerfont

Alternative Names: pexacerfont, bms-562086, bms562086, bms 562086
Latest Update: 2023-04-01
Latest Update Note: PubMed Publication

Product Description

Mechanisms of Action: CRFR Antagonist

Novel Mechanism: Yes

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: Bristol-Myers Squibb
Company Location: NEW YORK NY 10016
Company CEO: Giovanni Caforio
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Pexacerfont

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Phase 3: Generalized anxiety disorder

Phase 2: Alcoholism|Depressive Disorder, Major|Alcohol-Related Disorders|Irritable Bowel Syndrome

Phase 1: Taste Disorders|Hypertension|Weight Loss|Overweight

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

12-DA-N475

P1

Terminated

Taste Disorders|Overweight|Weight Loss|Hypertension

2015-09-01

11-AA-0010

P2

Completed

Alcohol-Related Disorders|Alcoholism

2014-07-01

CN148-015

P3

Completed

Generalized anxiety disorder

2008-03-01

CN148-007

P2

Completed

Depressive Disorder, Major

2007-10-01

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