Pegcetacoplan (APL-2) in Neovascular AMD
Part of paid clinical trials in Beverly Hills, California.
- Sponsor
- Apellis Pharmaceuticals, Inc.
- Study ID
- NCT03465709
- Phase
- PHASE1/PHASE2
- Status
- Terminated
Conditions
- Neovascular Age-related Macular Degeneration
Eligibility Criteria
- Sex
- ALL
- Age
- 60 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Pegcetacoplan — DRUGStudy Drug
Study Details
Safety Assessment of Pegcetacoplan in Patients with Neovascular AMD
Key Dates
- Start date
- Feb 14, 2018
- Status verified
- Sep 2020
- Primary completion
- Apr 5, 2019
- Completion
- Apr 5, 2019
Study Design
- Enrollment
- 17 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Pegcetacoplan Study Drug
Primary Outcome Measure
Number of Subjects Experiencing Ocular and Systemic Treatment-Emergent Adverse Events (TEAEs) Including by Maximum Severity [ Time Frame: Day 1 up to end of study (up to 1 year). ]
Locations (4)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Apellis Clinical Site | Beverly Hills | California | 90211 | - |
| Apellis Clinical Site | Hagerstown | Maryland | 21740 | - |
| Apellis Clinical Site | Cleveland | Ohio | 44122 | - |
| Apellis Clinical Site | Houston | Texas | 77030 | - |
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