Product Description
Mechanisms of Action: P2Y Agonist
Novel Mechanism: Yes
Modality: Small Molecule
Route of Administration: Ocular,Topical,Ophthalmic
FDA Designation: None *
Approval Status: Not Approved
Approved Countries: Indonesia | Korea | Malaysia | Philippines | Taiwan | Vietnam
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: Indonesia, Korea
Active Clinical Trial Count: 2
Highest Development Phases
Phase 3: Dry Eye Disease|Dry Eye Syndromes|Keratoconjunctivitis Sicca
Phase 2: Cataract
Trial |
Phase |
Trial Status |
Disease |
Primary Completion Date |
Probability of Success |
---|---|---|---|---|---|
TJO-083-A03 | P3 |
Recruiting |
Keratoconjunctivitis Sicca|Dry Eye Disease|Dry Eye Syndromes |
2024-12-31 |
38% |
NCT06146881 | P2 |
Recruiting |
Keratoconjunctivitis Sicca|Dry Eye Disease|Dry Eye Syndromes|Cataract |
2023-12-15 |