Asset profile

Eculizumab · Soliris

Monoclonal antibody

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Approvedregulatory verdict

Evidence outlook

Approved: paroxysmal nocturnal hemoglobinuria (PNH) to reduce hemolysis (FDA)

This approval is for an indication outside this terminal's covered markets; the covered program shown here is investigational. Regulatory approval supersedes design-level evidence grading for the approved use.

track record: Weak signal

Also in development:Hypertension

Source for the program status

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Competitive landscape

122 competitors in this universe: 1 direct rival (same mechanism and indication), 4 same-class, 117 same-indication; 33 further along in development.

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DrugStageModalityMechanismEvidence signalReported efficacygraded featured trials
Eculizumab (Soliris): this drugPhase 3Monoclonal antibodyComplement C5
Ravulizumab (Ultomiris)Phase 3Monoclonal antibodyComplement C5
Avacincaptad Pegol (Izervay)ApprovedRna AptamerComplement C5
CemdisiranPhase 3RNA / oligonucleotideComplement C5
PozelimabPhase 3Monoclonal antibodyComplement C5
ABBV-6628Phase 1/2Antibody fragmentComplement C5
Aprocitentan (Tryvio)ApprovedSmall moleculeEndothelin receptor (ETA/ETB, dual)
Atrasentan (Vanrafia)ApprovedSmall moleculeEndothelin A receptor
Avacopan (Tavneos)ApprovedSmall moleculeComplement C5a receptor 1 (C5aR1/CD88)
Baxdrostat (Baxfendy)ApprovedSmall moleculeAldosterone synthase (CYP11B2)
Bosentan (Tracleer)ApprovedSmall moleculeEndothelin receptor (ETA/ETB, dual)
Budesonide (targeted-Release) (TARPEYO / Nefecon)ApprovedSmall moleculeGlucocorticoid receptor
Canagliflozin (Invokana)ApprovedSmall moleculeSGLT2
Dapagliflozin (Farxiga / Forxiga)ApprovedSmall moleculeSGLT2
Daprodustat (Jesduvroq)ApprovedSmall moleculeHIF prolyl hydroxylase (HIF-PH1/2/3)
Difelikefalin (Korsuva)ApprovedPeptideKappa-opioid receptor (agonist, peripherally restricted)

…and 107 more. Research shows the complete landscape.

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Research adds each competitor's evidence grade and sourced trial results, aligned per race, so you can see who actually has the data.

Upcoming events

(9 total)

Estimated primary-completion dates from ClinicalTrials.gov. These are registry estimates, never confirmed readout dates; they can move as trials progress.

2026 (3)
October 2026 (1)
Phase 3Paroxysmal Nocturnal HemoglobinuriaActive not recruiting
Est. primary completion 2026-10-12 · NCT05133531 · CT.gov ↗
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December 2026 (2)
Phase 3NMOSD, Neuromyelitis Optica Spectrum DisordersActive not recruiting
Est. primary completion 2026-12-07 · NCT06724809 · CT.gov ↗
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Phase 3Neuromyelitis Optica Spectrum Disorders (NMOSD)Recruiting
Est. primary completion 2026-12-31 · NCT07420296 · CT.gov ↗
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2027 (3)
May 2027 (1)
Phase 3Paroxysmal Nocturnal Hemoglobinuria, PNH, Extravascular HemolysisRecruiting
Est. primary completion 2027-05-28 · NCT06449001 · CT.gov ↗
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June 2027 (1)
Phase 4Neuromyelitis Optica Spectrum Disorder AttackRecruiting
Est. primary completion 2027-06-30 · NCT07410039 · CT.gov ↗
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September 2027 (1)
Phase 2PNH - Paroxysmal Nocturnal HemoglobinuriaNot yet recruiting
Est. primary completion 2027-09 · NCT05731050 · CT.gov ↗
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2028 (1)
July 2028 (1)
Phase 2Transplant-Associated Thrombotic Microangiopathy (TA-TMA)Recruiting
Est. primary completion 2028-07-10 · NCT07707687 · CT.gov ↗
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2029 (1)
July 2029 (1)
Phase 2Paroxysmal Nocturnal HemoglobinuriaNot yet recruiting
Est. primary completion 2029-07 · NCT05646563 · CT.gov ↗
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2030 (1)
January 2030 (1)
Phase 4NMOSDRecruiting
Est. primary completion 2030-01 · NCT07010302 · CT.gov ↗
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See the full readout calendar ↗

All registered studies

Every ClinicalTrials.gov study of this drug's own program, grouped by indication and phase. Research unlocks the studies themselves: titles, statuses, dates and featured-trial cross-links.

Phase 3 (33)
Phase 2/3 (3)
Phase 2 (39)
Phase 1/2 (7)
Phase 1 (6)
Phase 4 (5)
Used as active comparator (13)
Appears in other studies (3)