TerminatedPhase 3NCT00642421
Safety and Biological Activity of C2L-OCT-01 PR in Acromegalic Patients
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
- Ambrilia Biopharma, Inc.
- Principal Investigator
- Raphael Naudin, M.D., M.DAmbrilia Biopharma, Inc.
- Intervention
- C2L-OCT-01 PR, 10 or 20 mg(drug)
- Enrollment
- 40 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2008 – 2009
Study locations (10)
- UCLA Medical Center Division of Neurosurgery, Los Angeles, California, United States
- Stanford University Medical Center, Stanford, California, United States
- Kaleida Health/Diabetes Center of WNY, Buffalo, New York, United States
- The Cleveland Clinic, Cleveland, Ohio, United States
- VA Puget Sound Health Care System, Tacoma, Washington, United States
- Republican Centre for Medical Rehabilitation and Water-therapy, Minsk, Belarus
- Semmelweis Egyetem Altalanos Orvostudomanyi, Budapest, Hungary
- Institute of Endocrinology "C.I. Parhon" Bucharest, Bucharest, Romania
- Institute of Endocrinology, University Clinical Center, Belgrade, Serbia
- V.P. Komisarenko Institute of Endocrinology and Metabolism, AMS Ukraine, Kiev, Ukraine
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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