CompletedPhase 1NCT02264639
A Phase I Study to Assess the Safety of Pegcetacoplan (APL-2) as an Add-On to Standard of Care in Subjects With PNH
Studying Paroxysmal nocturnal hemoglobinuria
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
- Apellis Pharmaceuticals, Inc.
- Principal Investigator
- Federico Grossi, MD, PhDApellis Pharmaceuticals, Inc.
- Intervention
- Pegcetacoplan(drug)
- Enrollment
- 9 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2015 – 2018
Study locations (7)
- University of Southern California Norris Comprehensive Cancer Center, Los Angeles, California, United States
- Lakes Research, Miami Lakes, Florida, United States
- University of Lousiville, Louisville, Kentucky, United States
- John Hopkins Hospital, Baltimore, Maryland, United States
- Cure 4 The Kids Foundation, Las Vegas, Nevada, United States
- Duke University Medical Center, Durham, North Carolina, United States
- Cleveland Clinic, Cleveland, Ohio, United States
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 NCT02264639 on ClinicalTrials.govOther trials for Paroxysmal nocturnal hemoglobinuria
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