CompletedPhase 2NCT05307328
SPI-62 as a Treatment for Adrenocorticotropic Hormone-dependent Cushing's Syndrome
Studying OBSOLETE: Cushing syndrome
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
- Sparrow Pharmaceuticals
- Principal Investigator
- Frank Czerwiec, MDSparrow Pharmaceuticals (info@sparrowpharma.com)
- Intervention
- SPI-62(drug)
- Enrollment
- 26 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2022 – 2025
Study locations (12)
- St. Joseph's Hospital and Medical Center - Barrow Neurological Institute (BNI) - Pituitary Center, Phoenix, Arizona, United States
- Southwest General Healthcare Center, Fort Myers, Florida, United States
- Mayo Clinic Cancer Center (MCCC) - Rochester, Rochester, Minnesota, United States
- Washington University School of Medicine - Center for Advanced Medicine (CAM), St Louis, Missouri, United States
- Comprehensive and Interventional Pain Management Llp, Henderson, Nevada, United States
- Memorial Sloan-Kettering Cancer Center, New York, New York, United States
- Oregon Health & Science University (OHSU) - Northwest Pituitary Center, Portland, Oregon, United States
- University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, United States
- Medical University of Plovdiv, Plovdiv, Bulgaria
- Clinical Center of Endocrinology and Gerontology, University Hospital of Endocrinology, Medical University Sofia (USHATE), Sofia, Bulgaria
- Medical University of Sofia, Sofia, Bulgaria
- Carol Davila University of Medicine and Pharmacy, Bucharest, Romania
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.
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