pegcetacoplan: Clinical Trials

31 trials of pegcetacoplan, newest first

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15 completed, 6 recruiting, 4 active not recruiting, 3 terminated. 11 Phase 2, 10 Phase 3, 8 Phase 1, 1 Phase 4.

By phase and status

PhaseTrialsStatus
Phase 211Completed 4, Recruiting 4, Terminated 2, Active not recruiting 1
Phase 310Completed 7, Active not recruiting 1, Recruiting 1, Withdrawn 1
Phase 18Completed 4, Terminated 2, Not yet recruiting 1, Recruiting 1
Phase 41Recruiting 1

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Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.

TrialPhaseStatusSponsorEnrollmentStartUpdated
A Study to Assess the Efficacy and Safety of Pegcetacoplan for the Prevention of Recurrent C3G or Primary IC-MPGN in Kidney Transplant Recipients
Pegcetacoplan - C3 Glomerulopathy (C3G), Primary Immune-Complex Membranoproliferative Glomerulonephritis (IC-MPGN), Recurrent Glomerular Disease After Kidney Transplantation
Phase 3RecruitingSwedish Orphan Biovitrum302027-01-212026-11-09
Safely Quenching Complement in Stroke Survivors
Pegcetacoplan Injection [Empaveli] - Acute Ischemic Stroke, Cerebral Infarction
Phase 1Not yet recruitingColumbia University202026-10-012026-04-29
Real-World Effectiveness and Safety of Pegcetacoplan in Patients With C3G or IC-MPG: A Multi-Country Study
Pegcetacoplan - C3 Glomerulopathy (C3G), Immune Complex Membranoproliferative Glomerulonephritis (IC-MPGN)
Phase 4RecruitingSwedish Orphan Biovitrum1502026-08-052026-09-09
Study to Evaluate the Efficacy and Safety of Pegcetacoplan in Adults at High Risk of Delayed Graft Function (DGF) Following Kidney Allograft Transplantation
Pegcetacoplan, Placebo - Delayed Graft Function, End Stage Renal Disease
Phase 3WithdrawnApellis Pharmaceuticals, Inc.2026-05-182026-09-02
Pegcetacoplan in Combination With Modified FOLFIRINOX for the Treatment of Metastatic Pancreatic Ductal Adenocarcinoma
Biopsy Procedure, Biospecimen Collection, Computed Tomography - Metastatic Pancreatic Ductal Adenocarcinoma, Stage IV Pancreatic Cancer AJCC v8
Phase 1 / Phase 2RecruitingRoswell Park Cancer Institute352026-02-162026-08-19
Study to Evaluate a Pegcetacoplan (Syfovre®) Prefilled Syringe
APL-2, Pegcetacoplan - Geographic Atrophy Secondary to Age-related Macular Degeneration
Phase 3CompletedApellis Pharmaceuticals, Inc.442025-10-242025-12-17
A Study to Investigate Safety, Tolerability, Pharmacokinetics (PK), Pharmacodynamics (PD), and Immunogenicity of RO7669330 in Participants With Geographic Atrophy (GA) Secondary to Age-related Macular Degeneration (AMD)
RO7669330, Syfovre™, Izervay™ - Geographic Atrophy, Age-related Macular Degeneration
Phase 1TerminatedHoffmann-La Roche272025-07-162026-11-04
A Phase 2, Randomized, Placebo Controlled, Multicenter, Masked Study to Evaluate the Efficacy, Safety, Tolerability, and Pharmacodynamics of Multidose APL 3007 in Combination With Syfovre/Pegcetacoplan (APL-2) in Patients Diagnosed With Geographic Atrophy Secondary to Age Related Macular Degeneratio
APL-3007, pegcetacoplan (APL-2), Placebo, Syfovre - Geographic Atrophy Secondary to Age-related Macular Degeneration
Phase 2RecruitingApellis Pharmaceuticals, Inc.2402025-06-232026-06-24
A Study to Test Whether BI 771716 Helps People With an Advanced Form of Age-related Macular Degeneration (AMD) Called Geographic Atrophy
BI 771716, Pegcetacoplan, Sham comparator to BI 771716 - Macular Degeneration, Age-related, Geographic Atrophy
Phase 2Active not recruitingBoehringer Ingelheim2022025-01-062026-05-14
A Prospective, Multicenter, Open-Label, Observational Phase 4 Study to Evaluate Real-World Safety, Tolerability, and Treatment Patterns of Pegcetacoplan (Syfovre) in Patients With Geographic Atrophy Secondary to Age-Related Macular Degeneration
Pegcetacoplan - Geographic Atrophy
Active not recruitingApellis Pharmaceuticals, Inc.3002023-09-282026-06-01
A Real World Effectiveness Study of Pegcetacoplan in Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH)
Pegcetacoplan - Paroxysmal Nocturnal Hemoglobinuria
Active not recruitingSwedish Orphan Biovitrum1652023-06-262026-09-03
An Open-Label, Nonrandomized, Multicenter Extension Study to Evaluate the Long-term Safety and Efficacy of Pegcetacoplan in Participants With C3 Glomerulopathy or Immune-Complex Membranoproliferative Glomerulonephritis
Pegcetacoplan - C3G, IC-MPGN
Phase 3Active not recruitingApellis Pharmaceuticals, Inc.1002023-05-292026-04-02
APL-2 and Pembrolizumab Versus APL-2, Pembrolizumab and Bevacizumab Versus Bevacizumab Alone for the Treatment of Recurrent Ovarian, Fallopian Tube, or Primary Peritoneal Cancer and Malignant Effusion
Bevacizumab, Biopsy, Biospecimen Collection - Fallopian Tube Carcinosarcoma, Fallopian Tube Clear Cell Adenocarcinoma
Phase 2RecruitingRoswell Park Cancer Institute602023-04-272026-03-23
A Study to Evaluate the Efficacy and Safety of Pegcetacoplan in Patients With Cold Agglutinin Disease (CAD)
Pegcetacoplan, Placebo matching Pegcetacoplan - Cold Agglutinin Disease
Phase 3CompletedSwedish Orphan Biovitrum242022-10-202025-10-30
A Study of Pegcetacoplan for Patients With Transplant-associated Thrombotic Microangiopathy After Hematopoietic Stem Cell Transplantation
Pegcetacoplan - Transplant-Associated Thrombotic Microangiopathy
Phase 2CompletedSwedish Orphan Biovitrum122022-02-012025-11-28
Phase III Study Assessing the Efficacy and Safety of Pegcetacoplan in Patients With C3 Glomerulopathy or Immune-Complex Membranoproliferative Glomerulonephritis
Pegcetacoplan, Placebo - C3G, IC-MPGN
Phase 3CompletedApellis Pharmaceuticals, Inc.1242021-11-122026-01-29
Study Assessing the Safety and Efficacy of Pegcetacoplan in Post-Transplant Recurrence of C3G or IC-MPGN
Pegcetacoplan - C3G, IC-MPGN
Phase 2CompletedApellis Pharmaceuticals, Inc.132021-09-072026-04-21
An Extension Study to Evaluate the Long-term Safety and Efficacy of Pegcetacoplan (APL-2) in Subjects With Geographic Atrophy Secondary to AMD
PEGCETACOPLAN (APL-2) - Geographic Atrophy Secondary to Age-related Macular Degeneration
Phase 3CompletedApellis Pharmaceuticals, Inc.7922021-03-042026-10-28
A Study of Pegcetacoplan in Pediatric Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH)
Pegcetacoplan - Paroxysmal Nocturnal Hemoglobinuria (PNH), Paroxysmal Hemoglobinuria
Phase 2RecruitingApellis Pharmaceuticals, Inc.122021-02-042026-06-26
MERIDIAN: A Study to Evaluate the Efficacy and Safety of Pegcetacoplan in Adults With Amyotrophic Lateral Sclerosis (ALS)
Pegcetacoplan (APL-2), Placebo - Amyotrophic Lateral Sclerosis, Motor Neuron Disease
Phase 2TerminatedApellis Pharmaceuticals, Inc.2492020-09-302025-04-24

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Conditions studied

Geographic Atrophy (7)  ·  Hemoglobinuria, Paroxysmal (6)  ·  Glomerulonephritis, Membranoproliferative (4)  ·  Anemia (3)  ·  Hematologic Diseases (3)  ·  Hemoglobinuria (3)  ·  Hemolysis (3)  ·  Macular Degeneration (3)  ·  Amyotrophic Lateral Sclerosis (1)  ·  Anemia, Hemolytic (1)  ·  Anemia, Hemolytic, Autoimmune (1)  ·  Cerebral Infarction (1)  ·  Delayed Graft Function (1)  ·  Fallopian Tube Neoplasms (1)  ·  Glomerulonephritis (1)

Sponsors

Apellis Pharmaceuticals, Inc. (21)  ·  Swedish Orphan Biovitrum (5)  ·  Roswell Park Cancer Institute (2)  ·  Boehringer Ingelheim (1)  ·  Columbia University (1)  ·  Hoffmann-La Roche (1)

Countries

United States (23)  ·  Spain (14)  ·  France (13)  ·  United Kingdom (13)  ·  Australia (12)  ·  Italy (11)  ·  Germany (10)  ·  Canada (9)  ·  Belgium (8)  ·  Czechia (8)  ·  Netherlands (8)  ·  Brazil (7)  ·  Japan (6)  ·  Poland (5)  ·  South Korea (5)

Top investigators

Federico Grossi, MD, PhD (4)  ·  Federico Grossi, MD PhD (2)  ·  Christos Fountzilas (1)  ·  E Sander Connolly, MD (1)  ·  Emese Zsiros (1)

Results publications

PMID 35869170, PMID 37314061, PMID 37707673, PMID 39079163, PMID 40720060, PMID 42133432, PMID 33730455, PMID 34445916, PMID 35113137, PMID 35796199, PMID 35860926, PMID 35869984, PMID 35948209, PMID 36055332, PMID 36284220, PMID 37715860, PMID 37865470, PMID 38315872, PMID 38573482, PMID 38593241, PMID 38722644, PMID 38727860, PMID 38752918, PMID 38814626, PMID 39522752, PMID 40280279, PMID 40285403, PMID 40388106, PMID 41337715, PMID 41533918

NIH funding

2023 (2), 2025 (1), R01CA267690 (1)