Last reviewed · How we verify

NCT05274633

Real Life Use of Ravulizumab in Italian Patients With Paroxysmal Nocturnal Hemoglobinuria

Completed Last updated 12 June 2025
What this trial tests

trial testing Ravulizumab in Paroxysmal Nocturnal Hemoglobinuria in 120 participants. Completed in 24 March 2025.

Timeline
17 June 2022
Primary endpoint
30 June 2024
24 March 2025

Quick facts

Lead sponsorAlexion Pharmaceuticals, Inc.
StatusCompleted
Study typeOBSERVATIONAL
Enrollment120
Start date17 June 2022
Primary completion30 June 2024
Estimated completion24 March 2025
Sites6 locations across Italy

Drugs / interventions tested

Conditions studied

Sponsor

Alexion Pharmaceuticals, Inc. — full company profile →

Who can join

18 and older, any sex, with Paroxysmal Nocturnal Hemoglobinuria. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study will collect clinical response data on participants who were already treated with eculizumab for at least 26 weeks and who started ravulizumab treatment as a specific therapeutic strategy as per ordinary clinical practice.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Real life use of ravulizumab in Italian patients with paroxysmal nocturnal hemoglobinuria: evidence from the REACTION observational study.
    Iori AP, De Vivo A, Di Bona E, Caocci G, et al · · 2026 · PMID 41566054 · DOI 10.1007/s00277-026-06792-w

Verify or expand the search:

Other trials of Ravulizumab

Trials testing the same drug.

Other recruiting trials for Paroxysmal Nocturnal Hemoglobinuria

Currently open trials in the same condition.

Other Alexion Pharmaceuticals, Inc. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05274633.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing