CompletedPhase 3NCT04076462
A Trial to Assess Efficacy and Safety of Octreotide Subcutaneous Depot in Patients With Acromegaly
Studying Acromegaly
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
- Camurus AB
- Principal Investigator
- Pamela Freda, M.DColumbia University
- Intervention
- CAM2029 (octreotide subcutaneous depot)(drug)
- Enrollment
- 72 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2019 – 2023
Study locations (30)
- UCLA Department of Medicine Division of Endocrinology, Los Angeles, California, United States
- Stanford University Medical Center, Palo Alto, California, United States
- Prufen Clinical Research LLC, Miami, Florida, United States
- University of Michigan, Ann Arbor, Michigan, United States
- Mayo Clinic, Rochester, Minnesota, United States
- Washington University in St. Louis, School of Medicine, St Louis, Missouri, United States
- Palm Research Center, Las Vegas, Nevada, United States
- Columbia University Medical Center, New York, New York, United States
- University of Cincinnati, Cincinnati, Ohio, United States
- Thomas Jefferson University, Philadelphia, Pennsylvania, United States
- Allegheny Endocrinology Associates, Pittsburgh, Pennsylvania, United States
- Research Institute of Dallas, Dallas, Texas, United States
- Universitätsklinikum Essen, Essen, Germany
- Universitätsklinikum Frankfurt, Medizinische Klinik 1, Schwerpunkt Endokrinologie, Diabetologie, Ernährungsmedizin, Frankfurt, Germany
- Universitätsklinikum Freiburg, Freiburg im Breisgau, Germany
- +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.
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