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Liafensine

Alternative Names: liafensine, bms-820836, bms820836, bms 820836, DB-104, DB104, DB 104
Latest Update: 2024-10-09
Latest Update Note: News Article

Product Description

Bristol-Myers Squibb is developing Liafensine as a treatment for Treatment Resistant Depression. (Sourced from: https://www.clinicaltrials.gov/study/NCT05113771)

Mechanisms of Action: NRI,SRI,DRI

Novel Mechanism: Yes

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: Fast Track - Depressive Disorder, Treatment-Resistant *

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 Liafensine

Countries in Clinic: Canada, China, United States

Active Clinical Trial Count: 2

Highest Development Phases

Phase 2: Depressive Disorder, Treatment-Resistant

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

ENLIGHTEN

P2

Completed

Depressive Disorder, Treatment-Resistant

2024-02-06

CTR20221896

P2

Not yet recruiting

Depressive Disorder, Treatment-Resistant

None

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