Product Description
Mechanisms of Action: PPAR-g Agonist
Novel Mechanism: No
Modality: Small Molecule
Route of Administration: Oral,Ophthalmic
FDA Designation: None *
Approval Status: Not Approved
Approved Countries: None
Approved Indications: None
Known Adverse Events: None
Company: Daiichi Sankyo
Company Location: TOKYO M0 103-8426
Company CEO:
Additonal Commercial Interests: None
Clinical Description
Countries in Clinic:
Active Clinical Trial Count:
Highest Development Phases
Phase 3: Type 2 Diabetes
Phase 2: Keratoconjunctivitis Sicca|Type 2 Diabetes|Dry Eye Syndromes|Dry Eye Disease
Trial |
Phase |
Trial Status |
Disease |
Primary Completion Date |
Probability of Success |
---|---|---|---|---|---|
NCT01468168 | P2 |
Completed |
Dry Eye Syndromes|Keratoconjunctivitis Sicca|Dry Eye Disease |
2012-11-01 |
|
NCT01118754 | P2 |
Completed |
Keratoconjunctivitis Sicca|Dry Eye Syndromes |
2010-12-01 |
|
JapicCTI-090916 | P2 |
Completed |
Keratoconjunctivitis Sicca |
2010-10-31 |
|
JapicCTI-090877 | P2 |
Completed |
Keratoconjunctivitis Sicca |
2009-08-31 |