Ozmosi | MK-0812 Drug Profile
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MK-0812

Alternative Names: mk-0812, mk0812, mk 0812
Clinical Status: Inactive
Latest Update: 2024-02-25
Latest Update Note: PubMed Publication

Product Description

Mechanisms of Action: CCL2 Antagonist

Novel Mechanism: Yes

Modality: Small Molecule

Route of Administration: N/A

FDA Designation: *

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
Additional Commercial Interests: None

Clinical Description

Countries in Clinic:

Active Clinical Trial Count:

Recent & Upcoming Milestones

Highest Development Phases

Phase 2: Multiple Sclerosis, Relapsing-Remitting|Arthritis, Rheumatoid

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT00239655

MK0812-003

P2

Terminated

Multiple Sclerosis, Relapsing-Remitting

2005-12-01

2022-05-04

Primary Endpoints|Treatments

NCT00542022

MK0812-008

P2

Completed

Arthritis, Rheumatoid

2005-05-01

2022-05-04

Primary Endpoints|Treatments