Ozmosi | Pexacerfont Drug Profile
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Pexacerfont

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

Product Description

Mechanisms of Action: CRFR Antagonist

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Bristol-Myers Squibb
Company Location: Eastern America
Company Founding Year: 1989
Additional Commercial Interests: None

Clinical Description

Countries in Clinic:

Active Clinical Trial Count:

Recent & Upcoming Milestones

Highest Development Phases

Phase 3: Generalized anxiety disorder

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

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

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT01656577

12-DA-N475

P1

Terminated

Weight Loss|Overweight|Hypertension|Taste Disorders

2015-09-01

2019-03-19

Treatments

NCT01227980

11-AA-0010

P2

Completed

Alcoholism|Alcohol-Related Disorders

2014-07-01

2019-03-22

Treatments

NCT00399438

CN148-013

P2

Completed

Irritable Bowel Syndrome

2007-10-01

2019-03-21

Treatments

NCT00135421

CN148-007

P2

Completed

Depressive Disorder, Major

2007-10-01

2019-03-21

Treatments

NCT00481325

CN148-015

P3

Completed

Generalized anxiety disorder

2008-03-01

2019-03-21

Treatments