Product Description
Mechanisms of Action: ADRA1A Agonist
Novel Mechanism: No
Modality: Small Molecule
Route of Administration: Intravenous
FDA Designation: None *
Approval Status: Approved
Approved Countries: Argentina | Australia | Brazil | India | Ireland | Italy | New Zealand | Pakistan | Saudi Arabia | Sri Lanka | Taiwan | Turkey | United Kingdom | Venezuela
Approved Indications: None
Known Adverse Events: None
Company: Zhejiang University
Company Location:
Company CEO:
Additonal Commercial Interests: None
Clinical Description
Countries in Clinic:
Active Clinical Trial Count:
Highest Development Phases
Phase 4: Acute Respiratory Distress Syndrome|Acute Lung Injury|Respiratory Distress Syndrome, Newborn|Hypertension|Cardiac Output, High|Pregnancy Outcomes|Cesarean Section|Stroke|Syncope|Bradycardia|Acidosis, Lactic|Hypotension
Phase 3: Pre-Eclampsia|Pregnancy Outcomes|Hypotension
Phase 2: Hypotension
Trial |
Phase |
Trial Status |
Disease |
Primary Completion Date |
Probability of Success |
---|---|---|---|---|---|
ChiCTR2400092788 | N/A |
Recruiting |
Heart Failure|Hypotension |
2026-12-31 |
|
ChiCTR2400091036 | N/A |
Not yet recruiting |
Cesarean Section|Hypotension |
2025-06-01 |
|
HEAD-START 2 | N/A |
Not yet recruiting |
Stroke |
2024-09-30 |
|
Effect of different administration modes of metaraminol on shivering and hypothermia after lumbar anesthesia during cesarean section | N/A |
Not yet recruiting |
Hypothermia|Cesarean Section |
2024-03-31 |