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MK-5757

Alternative Names: mk-5757, mk5757, mk 5757
Latest Update: 2015-11-01
Latest Update Note: Clinical Trial Update

Product Description

ORL1 antagonist (Sourced from: https://pubmed.ncbi.nlm.nih.gov/23238431/)

Mechanisms of Action: MR Modulator

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

Clinical Description

Map of Global Clinical Trials for MK-5757

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Phase 2: Cognitive Dysfunction|Schizophrenia

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success
NCT00848484

P2

Completed

Cognitive Dysfunction|Schizophrenia

2009-06-01

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