Product Description
Neurocrine is developing nbi-74788, an Oral CRFR Antagonist for Congenital Adrenal Hyperplasia. (Sourced from: https://clinicaltrials.gov/ct2/show/NCT04045145)
Mechanisms of Action: CRFR Antagonist
Novel Mechanism: Yes
Modality: Small Molecule
Route of Administration: Oral
FDA Designation: None *
Approval Status: Not Approved
Approved Countries: None
Approved Indications: None
Known Adverse Events: None
Company: Neurocrine
Company Location: SAN DIEGO CA 92130
Company CEO: Kevin C. Gorman
Additonal Commercial Interests: None
Clinical Description
Countries in Clinic: Austria, Belgium, Bulgaria, Canada, Czech Republic, France, Germany, Greece, Israel, Italy, Netherlands, Poland, Portugal, Serbia, Spain, Sweden, United Kingdom, United States
Active Clinical Trial Count: 5
Highest Development Phases
Phase 3: Adrenal Hyperplasia, Congenital|Adrenocortical Hyperfunction|Adrenogenital Syndrome
Trial |
Phase |
Trial Status |
Disease |
Primary Completion Date |
Probability of Success |
---|---|---|---|---|---|
NBI-74788-CAH2006 | P3 |
Unknown Status |
Adrenal Hyperplasia, Congenital |
2027-10-31 |
|
NBI-74788-CAH3003 | P3 |
Unknown Status |
Adrenal Hyperplasia, Congenital |
2027-08-31 |
|
2020-004381-19 | P3 |
Active, not recruiting |
Adrenal Hyperplasia, Congenital |
2024-04-15 |
|
CAHtalyst | P3 |
Active, not recruiting |
Adrenogenital Syndrome|Adrenal Hyperplasia, Congenital|Adrenocortical Hyperfunction |
2023-07-19 |