Product Description
Mechanisms of Action: NMDA Antagonist
Novel Mechanism: No
Modality: Small Molecule
Route of Administration: Intravenous,Oral
FDA Designation: None *
Approval Status: Not Approved
Approved Countries: None
Approved Indications: None
Known Adverse Events: None
Company: AstraZeneca
Company Location: CAMBRIDGE X0 CB2 0AA
Company CEO: Pascal Soriot
Additonal Commercial Interests: None
Clinical Description
Countries in Clinic:
Active Clinical Trial Count:
Highest Development Phases
Phase 2: Depressive Disorder, Major|Depressive Disorder, Treatment-Resistant
Phase 1: Depressive Disorder, Major|Healthy Volunteers|Stress Disorders, Post-Traumatic|Depressive Disorder
Trial |
Phase |
Trial Status |
Disease |
Primary Completion Date |
Probability of Success |
---|---|---|---|---|---|
1R61MH110540-01 | P1 |
Completed |
Stress Disorders, Post-Traumatic|Depressive Disorder |
2019-11-12 |
|
D6702C00031 | P2 |
Completed |
Depressive Disorder, Major |
2013-08-26 |
|
2011-004690-87 | P2 |
Completed |
Depressive Disorder, Major |
2013-08-23 |
|
D6702C00015 | P2 |
Completed |
Depressive Disorder, Major|Depressive Disorder, Treatment-Resistant |
2011-12-01 |