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Study identifier: NCT05307328 Synced from ClinicalTrials.gov · August 03, 2026
● Completed

SPI-62 as a Treatment for Adrenocorticotropic Hormone-dependent Cushing's Syndrome

Condition: Cushing's Syndrome I · Cushing Disease Due to Increased ACTH Secretion · Cortisol Excess  ·  Sponsor: Sparrow Pharmaceuticals

PhasePhase 2
Planned participants26
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This is a randomized, placebo-controlled, study of SPI-62 in subjects with ACTH-dependent Cushing's syndrome caused by a non-adrenal tumor. Subjects will receive each of the following 2 treatments for 24 weeks: SPI-62 and matching placebo with the option of long-term extension.

This description comes directly from the study's public registry record.

Talk to the study team

No contact information is available for this study as per the public registry record.

Always discuss trial participation with your own doctor first.

Locations (12)

St. Joseph's Hospital and Medical Center - Barrow Neurological Institute (BNI) - Pituitary CenterPhoenix, Arizona, United States
Southwest General Healthcare CenterFort Myers, Florida, United States
Mayo Clinic Cancer Center (MCCC) - RochesterRochester, Minnesota, United States
Washington University School of Medicine - Center for Advanced Medicine (CAM)St Louis, Missouri, United States
Comprehensive and Interventional Pain Management LlpHenderson, Nevada, United States
Memorial Sloan-Kettering Cancer CenterNew York, New York, United States
Oregon Health & Science University (OHSU) - Northwest Pituitary CenterPortland, Oregon, United States
University of Pittsburgh Medical CenterPittsburgh, Pennsylvania, United States
Medical University of PlovdivPlovdiv, Bulgaria
Clinical Center of Endocrinology and Gerontology, University Hospital of Endocrinology, Medical University Sofia (USHATE)Sofia, Bulgaria
Medical University of SofiaSofia, Bulgaria
Carol Davila University of Medicine and PharmacyBucharest, Romania

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