Ozmosi | MK-0359 Drug Profile
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MK-0359

Alternative Names: mk-0359, mk0359, mk 0359
Clinical Status: Inactive
Latest Update: 2015-12-02
Latest Update Note: Clinical Trial Update

Product Description

MK-0359 is a potent and selective, oral PDE4 inhibitor that has a competitive and reversible mode of interaction. (Sourced from: https://www.guidetopharmacology.org/GRAC/LigandDisplayForward?tab=clinical&ligandId=9852)

Mechanisms of Action: PDE4 Inhibitor

Novel Mechanism: No

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: Eastern America
Company Founding Year: 1668
Additional Commercial Interests: None

Clinical Description

Countries in Clinic:

Active Clinical Trial Count:

Recent & Upcoming Milestones

Highest Development Phases

Phase 2: Arthritis, Rheumatoid|Asthma|Chronic Obstructive Pulmonary Disease

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT00482417

NCT00482417

P2

Completed

Arthritis, Rheumatoid

2003-05-01

2022-05-04

Treatments

NCT00482235

NCT00482235

P2

Completed

Chronic Obstructive Pulmonary Disease

2003-04-01

2022-05-04

Treatments

NCT00482898

MK0359-013

P2

Completed

Asthma

2003-04-01

2022-05-04

Treatments

Recent News Events

Date

Type

Title