Product Description
Mechanisms of Action: 5-HT2 Antagonist,GPIIb/IIIa Inhibitor
Novel Mechanism: No
Modality: Small Molecule
Route of Administration: Oral,Intravenous,Sublingual
FDA Designation: None *
Approval Status: Not Approved
Approved Countries: Austria | Dominican Republic | Germany | Ireland | Italy | Mexico | Portugal | Taiwan | United Kingdom | Venezuela
Approved Indications: None
Known Adverse Events: None
Company: Medisch Centrum Leeuwarden
Company Location:
Company CEO:
Additonal Commercial Interests: None
Clinical Description
Countries in Clinic:
Active Clinical Trial Count:
Highest Development Phases
Phase 4: Other|Hypertension
Phase 3: Sepsis|Kidney Diseases|Shock, Septic|Acute Kidney Injury
Phase 1: Consciousness Disorders|Depressive Disorder, Treatment-Resistant|Headache Disorders, Primary|Psychotic Disorders|Cluster Headache|Depressive Disorder
Trial |
Phase |
Trial Status |
Disease |
Primary Completion Date |
Probability of Success |
---|---|---|---|---|---|
LBL | P1 |
Recruiting |
Depressive Disorder, Treatment-Resistant|Consciousness Disorders|Cluster Headache|Psychotic Disorders|Headache Disorders, Primary |
2025-06-30 |
|
L-Ket | P1 |
Completed |
Depressive Disorder |
2021-08-28 |
|
KoPTaL | P4 |
Unknown status |
Hypertension |
2019-04-01 |
|
KoPTaL | P4 |
Active, not recruiting |
Other |
2019-03-02 |