Product Description
Mechanisms of Action: ER Modulator
Novel Mechanism: No
Modality: Small Molecule
Route of Administration: Oral,Vaginal
FDA Designation: None *
Approval Status: Not Approved
Approved Countries: European Medicines Agency | Ireland | Portugal | Sweden
Approved Indications: None
Known Adverse Events: None
Company: Sermonix Pharmaceuticals
Company Location:
Company CEO:
Additonal Commercial Interests: Henlius Biotech
Clinical Description
Countries in Clinic: Australia, Belgium, Canada, China, Czech Republic, France, Germany, Hungary, Israel, Italy, Korea, Poland, Romania, Singapore, Spain, Taiwan, Turkey, United Kingdom, United States
Active Clinical Trial Count: 6
Highest Development Phases
Phase 3: Breast Cancer
Phase 2: Dyspareunia|Multiple System Atrophy
Trial |
Phase |
Trial Status |
Disease |
Primary Completion Date |
Probability of Success |
---|---|---|---|---|---|
ELAINEIII | P3 |
Recruiting |
Breast Cancer |
2027-04-01 |
|
SMX 22-002 | P3 |
Unknown Status |
Breast Cancer |
2026-10-30 |
|
ELAINEII | P2 |
Active, not recruiting |
Breast Cancer |
2024-12-31 |
|
SMX 18001 | P2 |
Active, not recruiting |
Breast Cancer |
2024-12-01 |
57% |