Active, not recruitingPhase 3NCT04806451
Global Safety and Efficacy Registration Study of Crinecerfont in Pediatric Participants With Classic Congenital Adrenal Hyperplasia (CAHtalyst Pediatric Study)
Studying Congenital adrenal hyperplasia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Neurocrine Biosciences
- Principal Investigator
- Clinical Development LeadNeurocrine Biosciences
- Intervention
- Crinecerfont(drug)
- Enrollment
- 103 enrolled
- Eligibility
- 2-17 years · All sexes
- Timeline
- 2021 – 2027
Study locations (30)
- Neurocrine Clinical Site, Birmingham, Alabama, United States
- Neurocrine Clinical Site, Los Angeles, California, United States
- Neurocrine Clinical Site, Orange, California, United States
- Neurocrine Clinical Site, San Diego, California, United States
- Neurocrine Clinical Site, San Francisco, California, United States
- Neurocrine Clinical Site, Aurora, Colorado, United States
- Neurocrine Clinical Site, Hartford, Connecticut, United States
- Neurocrine Clinical Site, Washington D.C., District of Columbia, United States
- Neurocrine Clinical Site, Atlanta, Georgia, United States
- Neurocrine Clinical Site, Indianapolis, Indiana, United States
- Neurocrine Clinical Site, Boston, Massachusetts, United States
- Neurocrine Clinical Site, Ann Arbor, Michigan, United States
- Neurocrine Clinical Site, Minneapolis, Minnesota, United States
- Neurocrine Clinical site, St Louis, Missouri, United States
- Neurocrine Clinical Site, New Hyde Park, New York, United States
- +15 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT04806451 on ClinicalTrials.govOther trials for Congenital adrenal hyperplasia
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