Product Description
Mechanisms of Action: CRTH2 Antagonist
Novel Mechanism: Yes
Modality: Small Molecule
Route of Administration: Oral
FDA Designation: None *
Approval Status: Not Approved
Approved Countries: Brazil | Chile | Colombia | Dominican Republic | Germany | Hungary | India | Ireland | Italy | New Zealand | Russia | United Kingdom
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
Countries in Clinic:
Active Clinical Trial Count:
Highest Development Phases
Phase 4: Atherosclerosis|Hypercholesterolemia|Dyslipidemia|Inflammation|Type 2 Diabetes|Coronary Artery Disease|Oxidative Stress|Hyperlipoproteinemias|Hyperlipidemia|Myocardial Ischemia
Phase 3: Dyslipidemia|Hyperlipidemia|Type 2 Diabetes|Hyperlipoproteinemias|Lipidoses|Hypercholesterolemia|Hyperlipoproteinemia Type V|Intermittent Claudication|Peripheral Arterial Disease|Stroke|Myocardial Infarction|Hyperlipoproteinemia Type II|Coronary Artery Disease|Coronary Disease|Myocardial Ischemia|Peripheral Vascular Diseases
Phase 2: Asthma|Rhinitis, Allergic, Seasonal|Dyslipidemia|Hypercholesterolemia|Flushing
Phase 1: Dyslipidemia|Type 2 Diabetes|Hypercholesterolemia|Rosacea|Hyperlipidemia|Hyperlipoproteinemia Type II
Trial |
Phase |
Trial Status |
Disease |
Primary Completion Date |
Probability of Success |
---|---|---|---|---|---|
NILACH | P4 |
Terminated |
Atherosclerosis |
2014-07-01 |
|
MK-0524A-119 | N/A |
Terminated |
Hypercholesterolemia|Dyslipidemia |
2013-05-01 |
|
2011-000755-17 | P3 |
Terminated |
Coronary Disease |
2013-03-08 |
|
MK-0524A-133 | P3 |
Terminated |
Dyslipidemia|Hypercholesterolemia |
2013-02-26 |