Soliris: Clinical Trials

46 trials of Soliris, newest first

ClinicalTrials Daily  ·  Areas  ·  Conditions  ·  Drugs  ·  Sponsors  ·  

26 completed, 12 terminated, 3 unknown, 2 withdrawn. 28 Phase 2, 13 Phase 3, 10 Phase 1, 1 Phase 4.

By phase and status

PhaseTrialsStatus
Phase 228Completed 13, Terminated 10, Unknown 2, Withdrawn 2, Not yet recruiting 1
Phase 313Completed 9, Terminated 3, Active not recruiting 1
Phase 110Completed 5, Terminated 2, Unknown 2, Withdrawn 1
Phase 41Completed 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
Study of NM8074 in Adult PNH Patients With Inadequate Response to Soliris
NM8074, Soliris - Paroxysmal Nocturnal Hemoglobinuria
Phase 2Not yet recruitingNovelMed Therapeutics122027-01-012026-04-13
Eculizumab for Prevention of Antibody-Mediated Rejection in ABO-Incompatible Living Donor Kidney Transplantation
Eculizumab - Kidney Transplantation
Phase 1 / Phase 2UnknownTao Lin302024-07-012024-06-13
Efficacy and Safety of the Combination of Pozelimab and Cemdisiran Versus Continued Eculizumab or Ravulizumab Treatment in Adult Patients With Paroxysmal Nocturnal Hemoglobinuria
Cemdisiran, Eculizumab, Pozelimab - Paroxysmal Nocturnal Hemoglobinuria
Phase 3TerminatedRegeneron Pharmaceuticals32022-10-062025-04-08
A Study to Evaluate How Safe Pozelimab + Cemdisiran Combination Therapy is and How Well it Works in Adult Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH) Who Have Not Recently Received or Have Not Received Complement Inhibitor Treatment
Ravulizumab, Pozelimab, Cemdisiran - Paroxysmal Nocturnal Hemoglobinuria
Phase 3Active not recruitingRegeneron Pharmaceuticals2022022-08-012026-04-30
BCX9930 for the Treatment of Paroxysmal Nocturnal Hemoglobinuria (PNH) in Participants With Inadequate Response to C5 Inhibitor Therapy
Eculizumab, Ravulizumab, BCX9930 - Paroxysmal Nocturnal Hemoglobinuria (PNH)
Phase 2TerminatedBioCryst Pharmaceuticals122021-12-062025-03-07
Renal Function in Highly Sensitized Patients 1 Year After Desensitization With Imlifidase Prior to DD Kidney Tx
Imlifidase, PLEX, IVIg - Kidney Transplantation in Highly Sensitized Patients
Phase 3CompletedHansa Biopharma AB642021-10-142026-04-30
Complement Regulation to Undo Systemic Harm in Preeclampsia
Eculizumab - Preeclampsia, Severe Preeclampsia
Phase 2TerminatedCedars-Sinai Medical Center22021-09-132023-11-29
Ravulizumab in Adult Participants With Paroxysmal Nocturnal Hemoglobinuria Currently Treated With High-Dose Eculizumab
Eculizumab, Ravulizumab - Paroxysmal Nocturnal Hemoglobinuria
Phase 4CompletedAlexion Pharmaceuticals, Inc.182021-04-142024-09-05
A Study to Evaluate the Efficacy and Safety of Eculizumab in Guillain-Barré Syndrome
Eculizumab, Placebo - Guillain-Barre Syndrome
Phase 3CompletedAlexion Pharmaceuticals, Inc.572021-03-082025-09-08
The Use of Eculizumab in HELLP Syndrome
Eculizumab - HELLP Syndrome (HELLP), Third Trimester, Complement Abnormality
Phase 1CompletedJohns Hopkins University32021-02-232023-11-14
A Study of the Safety and Activity of Eculizumab in Pediatric Participants With Relapsing Neuromyelitis Optica Spectrum Disorder
Eculizumab - Neuromyelitis Optica, Neuromyelitis Optica Spectrum Disorder
Phase 2 / Phase 3TerminatedAlexion Pharmaceuticals, Inc.52020-01-142024-09-25
Clinical Trial of BCD-148 and Soliris® for the Treatment of Patients With Paroxysmal Nocturnal Hemoglobinuria
BCD-148, Soliris - Paroxysmal Nocturnal Hemoglobinuria
Phase 3CompletedBiocad282019-04-042021-02-12
A Study Evaluating the Efficacy and Safety of ABP 959 Compared With Eculizumab in Adult Participants With PNH
ABP 959, Eculizumab - Paroxysmal Nocturnal Hemoglobinuria
Phase 3CompletedAmgen422019-01-222023-05-23
Comparative Study of Pharmacokinetics, Pharmacodynamics, Safety, and Immunogenicity of Single Intravenous Doses of BCD-148 and Soliris®
BCD-148, Soliris - Healthy Subjects
Phase 1CompletedBiocad782018-09-212020-05-15
Eculizumab to Treat Thrombotic Microangiopathy/Atypical Hemolytic Uremic Syndrome -Associated Multiple Organ Dysfunction Syndrome in Hematopoietic Stem Cell Transplant Recipients
Eculizumab - Thrombotic Microangiopathies, Atypical Hemolytic Uremic Syndrome
Phase 2CompletedChildren's Hospital Medical Center, Cincinnati232018-08-032023-09-21
Transcriptome and Metabolic Analyses of CHAPLE Disease
Eculizumab Injection - CD55 - Cluster of Differentiation Antigen 55 Deficiency, Primary Intestinal Lymphangiectasis
UnknownMarmara University602018-06-152019-08-14
Study to Evaluate the Efficacy and Safety of APL-2 in Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH)
Pegcetacoplan, Soliris - Paroxysmal Nocturnal Hemoglobinuria
Phase 3CompletedApellis Pharmaceuticals, Inc.802018-06-142022-03-25
Study of Danicopan in Participants With Paroxysmal Nocturnal Hemoglobinuria With Inadequate Response to Eculizumab
Danicopan, Eculizumab - Paroxysmal Nocturnal Hemoglobinuria (PNH)
Phase 2CompletedAlexion Pharmaceuticals, Inc.122018-05-082023-12-12
Complement Inhibitor Eculizumab in Clinical Islet Transplantation
Eculizumab - Diabetes Mellitus
Phase 2CompletedUppsala University32016-05-152018-10-04
Eculizumab Therapy for Subclinical Antibody-mediated Rejection in Kidney Transplantation
Eculizumab - Subclinical Acute Antibody-mediated Rejection in Kidney Transplantation
Phase 1 / Phase 2WithdrawnAssistance Publique - Hôpitaux de Paris2015-02-012025-11-20

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Conditions studied

Hemoglobinuria, Paroxysmal (12)  ·  Neuromyelitis Optica (4)  ·  Delayed Graft Function (3)  ·  Demyelinating Diseases (3)  ·  Myelitis, Transverse (3)  ·  Optic Neuritis (3)  ·  Recurrence (3)  ·  HELLP Syndrome (2)  ·  Kidney Failure, Chronic (2)  ·  Rejection, Psychology (2)  ·  Thrombotic Microangiopathies (2)  ·  Acute Lung Injury (1)  ·  Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis (1)  ·  Antiphospholipid Syndrome (1)  ·  Atypical Hemolytic Uremic Syndrome (1)

Sponsors

Alexion Pharmaceuticals, Inc. (14)  ·  Mayo Clinic (3)  ·  Biocad (2)  ·  Cedars-Sinai Medical Center (2)  ·  Johns Hopkins University (2)  ·  Regeneron Pharmaceuticals (2)  ·  Amgen (1)  ·  Apellis Pharmaceuticals, Inc. (1)  ·  Assistance Publique - Hôpitaux de Paris (1)  ·  BioCryst Pharmaceuticals (1)  ·  Brigham and Women's Hospital (1)  ·  Children's Hospital Medical Center, Cincinnati (1)  ·  Hadassah Medical Organization (1)  ·  Hansa Biopharma AB (1)  ·  Heeger, Peter, M.D. (1)

Countries

United States (30)  ·  Italy (12)  ·  United Kingdom (12)  ·  Spain (11)  ·  France (8)  ·  Australia (7)  ·  Canada (7)  ·  Germany (7)  ·  Japan (6)  ·  Russia (6)  ·  South Korea (5)  ·  Sweden (5)  ·  Turkey (Türkiye) (5)  ·  Czechia (4)  ·  Malaysia (3)

Top investigators

Anil K Chandraker, MD (1)  ·  Arthur J Vaught (1)  ·  Austin G Kulasekararaj, MBBS, MD (1)  ·  Benjamin Philosophe, MD, PHD (1)  ·  Bernd Schroppel, MD (1)  ·  Dror Mevorach, MD (1)  ·  Gunnar Tufveson, MD, PhD (1)  ·  Jeffrey Laurence, MD (1)  ·  Jignesh Patel, M.D., Ph.D. (1)  ·  Mark D Stegall (1)  ·  Mark D. Stegall, M.D. (1)

Results publications

PMID 33676197, PMID 34498507, PMID 17702897, PMID 21222185, PMID 21942930, PMID 23512355, PMID 23623397, PMID 23934275, PMID 24289920, PMID 24354307, PMID 24408973, PMID 24990476, PMID 25654478, PMID 27568864, PMID 30887675, PMID 31050279, PMID 32990324, PMID 33251691, PMID 33310418, PMID 33730455, PMID 34314483, PMID 34445916, PMID 34803867, PMID 35514201, PMID 35796199, PMID 35869984, PMID 36055332, PMID 37182818, PMID 37314061, PMID 37707673, PMID 37946262, PMID 38593241, PMID 38727860, PMID 38987228, PMID 39079163, PMID 39171864, PMID 40285403, PMID 40720060, PMID 42763038

NIH funding

2019 (2), 2014 (1), 2016 (1), 2023 (1), K12HD085845 (1), P01DK058335 (1), UL1TR000135 (1), ZIAAI000717-22 (1)