Evidence map›Paper›PMID 39841198›Full record

Trial reportAnnals of hematology2025

Ravulizumab demonstrates long-term efficacy, safety and favorable patient survival in patients with paroxysmal nocturnal hemoglobinuria.

Austin Kulasekararaj, Robert Brodsky, Hubert Schrezenmeier, Morag Griffin, Alexander Röth, Caroline Piatek, Masayo Ogawa, Ji Yu, Ami S Patel, Yogesh Patel and 8 more

3 registry-linked trialsAbstract readClinical Trial, Phase IIIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Annals of hematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT01374360 completednot on this map

Paroxysmal Nocturnal Hemoglobinuria (PNH) Registry

TypeobservationalSponsorAlexion Pharmaceuticals, Inc.Ran2004 to 2025Enrolled6,061ConditionsParoxysmal Nocturnal Hemoglobinuria
NCT02946463 phase3completednot on this map

A Phase 3, Randomized, Open-Label, Active-Controlled Study of ALXN1210 Versus Eculizumab in Complement Inhibitor-Naïve Adult Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH)

TypeinterventionalSponsorAlexion Pharmaceuticals, Inc.Ran2016 to 2023Enrolled272ConditionsParoxysmal Nocturnal Hemoglobinuria (PNH)ArmsRavulizumab, Eculizumab
NCT03056040 phase3completednot on this map

A Phase 3, Randomized, Open-Label, Active-Controlled Study of ALXN1210 Versus Eculizumab in Adult Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH) Currently Treated With Eculizumab

TypeinterventionalSponsorAlexion Pharmaceuticals, Inc.Ran2017 to 2022Enrolled202ConditionsParoxysmal Nocturnal Hemoglobinuria (PNH)ArmsRavulizumab, Eculizumab
3 · Its place in the literature

Who cites it

18 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Observational
  5. Article
  6. Review
  7. Article
  8. Observational
  9. Article
  10. Article
  11. Article
  12. Review
  13. The varieties of therapeutic experience: navigating treatment options for patients with PNH.Hematology. American Society of Hematology. Education Program · 2025
    Review
  14. Review
  15. Observational
  16. Review
  17. Article
  18. First reported case ofIDCases · 2025
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors.

Austin KulasekararajDepartment of Haematological Medicine, King's College Hospital, National Institute for Health Research and Wellcome King's Clinical Research Facility and King's College London, London, UK. austin.kulasekararaj@nhs.net.
Robert BrodskyDivision of Hematology, Johns Hopkins Medicine, Baltimore, MD, USA.
Hubert SchrezenmeierInstitute of Transfusion Medicine, University of Ulm, Ulm, Germany.
Morag GriffinSt James's Hospital, NHS Teaching Hospitals, Leeds, UK.
Alexander RöthWest German Cancer Center, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
Caroline PiatekJane Anne Nohl Division of Hematology and Center for the Study of Blood Diseases, USC Norris Comprehensive Cancer Center, Los Angeles, CA, USA.
Masayo OgawaAlexion, AstraZeneca Rare Disease, Boston, MA, USA.
Ji YuAlexion, AstraZeneca Rare Disease, Boston, MA, USA.
Ami S PatelAlexion, AstraZeneca Rare Disease, Boston, MA, USA.
Yogesh PatelAlexion, AstraZeneca Rare Disease, Boston, MA, USA.
Rosario NotaroCore Research Laboratory, Istituto per lo Studio, la Prevenzione e la Rete Oncologica (ISPRO), Florence, Italy.
Kensuke UsukiNTT Medical Center Tokyo, Tokyo, Japan.
Alexander KulaginRM Gorbacheva Research Institute, Pavlov University, St Petersburg, Russia.
Sandra GualandroDepartment of Hematology, University of São Paulo Medical School, São Paulo, Brazil.
Wolfgang FürederDivision of Hematology and Hemostaseology, Department of Internal Medicine I, Medical University of Vienna, Vienna, Austria.
Regis Peffault de LatourAssistance Publique- Hôpitaux de Paris, Saint-Louis Hospital, Paris, France.
Jeff SzerDepartment of Clinical Haematology, Peter MacCallum Cancer Centre and the Royal Melbourne Hospital, Melbourne, VIC, Australia.
Jong Wook LeeDivision of Hematology-Oncology, Hanyang University Seoul Hospital, Seoul, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ravulizumab is a second-generation complement component 5 (C5) inhibitor (C5i) approved for the treatment of paroxysmal nocturnal hemoglobinuria (PNH) following positive results from two pivotal trials in patients with PNH originally naive to C5i treatment and eculizumab-experienced patients with PNH. In both trials, after the 26week primary evaluation period, all patients received ravulizumab for up to 6 years. To report ravulizumab treatment outcomes in patients with PNH originally naive to C5i treatment and eculizumab-experienced patients with PNH treated for up to 6 years. Originally C5i-naive (N = 244) and eculizumab-experienced (N = 191) patients with PNH continued ravulizumab treatment for up to 6 years. Major adverse vascular events (MAVEs; including thrombotic events [TEs]) and survival are reported, including a comparison of survival with untreated patients from the International PNH Registry. Laboratory parameters for intravascular hemolysis (IVH) are also described. For up to 6 years (1468.0 patient-years of exposure), ravulizumab provided durable control of terminal complement activity and IVH, resulting in a low incidence of MAVEs (including TEs) reported (MAVE rate: 0.7-1.4 per 100 patient-years) and, compared with untreated patients from the International PNH Registry, reduced the risk of mortality by five-fold. The few breakthrough IVH events reported (N = 122) were commonly associated with complement-amplifying conditions, and only two events (1.8%) were associated with suboptimal inhibition of C5 (i.e. serum free C5 ≥ 0.5 µg/mL). These results support the long-term use of ravulizumab as the first-line treatment of choice for patients with PNH. Trial registration details: NCT01374360; registered: October 29, 2004; NCT02946463; registered: October 27, 2016; NCT03056040; registered: June 05, 2017.

Indexed as

Antibodies, Monoclonal, HumanizedComplement Inactivating AgentsHemoglobinuria, ParoxysmalAdultAgedComplement C5FemaleFollow-Up StudiesHemolysisHumansMaleMiddle AgedSurvival RateTreatment OutcomeYoung AdultAntibodies, Monoclonal, HumanizedComplement C5Complement Inactivating AgentseculizumabravulizumabComplement inhibitorIntravascular hemolysisLactate dehydrogenaseParoxysmal nocturnal hemoglobinuriaRavulizumabSurvival

Identifiers

PMID39841198
PMCPMC11868214

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.