Product Description
Mechanisms of Action: P2Y2 Agonist
Novel Mechanism: Yes
Modality: Small Molecule
Route of Administration: Oral,Topical,Inhalant,Injection
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
Countries in Clinic:
Active Clinical Trial Count:
Highest Development Phases
Phase 3: Cystic Fibrosis|Pulmonary Fibrosis
Phase 2: Pulmonary Fibrosis|Cystic Fibrosis|Macular Edema|Retinal Detachment|Uveitis|Rhinitis, Allergic, Perennial|Cataract
Phase 1: Healthy Volunteers|Retinal Detachment
Trial |
Phase |
Trial Status |
Disease |
Primary Completion Date |
Probability of Success |
---|---|---|---|---|---|
DEFY | P3 |
Terminated |
Cystic Fibrosis |
2011-02-01 |
|
P08640 | P3 |
Completed |
Cystic Fibrosis |
2010-10-01 |
|
REACH-1 | P2 |
Completed |
Cystic Fibrosis |
2010-10-01 |
|
NCT00357279 | P3 |
Completed |
Cystic Fibrosis|Pulmonary Fibrosis |
2008-09-01 |