Product Description
Celiprolol is a beta 1-selective adrenoceptor antagonist (beta-blocker) which acts as a weak agonist at beta 2-adrenoceptors. The drug demonstrates vasodilator properties and does not depress heart rate to the same extent as propranolol, atenolol or metoprolol. (Sourced from: https://pubmed.ncbi.nlm.nih.gov/8573993/#:~:text=Celiprolol%20is%20a%20beta%201,as%20propranolol%2C%20atenolol%20or%20metoprolol.)
Mechanisms of Action: ADRB1 Antagonist
Novel Mechanism: No
Modality: Small Molecule
Route of Administration: Oral
FDA Designation: Breakthrough Therapy - Ehlers-Danlos Syndrome *
Approval Status: Not Approved
Approved Countries: Bangladesh | Belgium | Chile | Colombia | Czech | Egypt | Finland | France | Germany | Greece | Hungary | India | Ireland | Italy | Korea | Lithuania | Netherlands | New Zealand | Peru | Poland | Portugal | Slovakia | Slovenia | Spain | Sweden | Switzerland | Tunisia | United Kingdom
Approved Indications: None
Known Adverse Events: None
Company: Acer Therapeutics
Company Location: NEWTON MA 02458
Company CEO: Chris Schelling
Additonal Commercial Interests: None
Clinical Description
Countries in Clinic: United States
Active Clinical Trial Count: 1
Highest Development Phases
Phase 3: Ehlers-Danlos Syndrome
Trial |
Phase |
Trial Status |
Disease |
Primary Completion Date |
Probability of Success |
---|---|---|---|---|---|
DiSCOVER | P3 |
Recruiting |
Ehlers-Danlos Syndrome |
2029-03-01 |
72% |