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NCT06903234Active, not recruiting

Post-authorization Safety Study of Iptacopan in Adult Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH) Using Data From the IPIG PNH Registry

Post-authorization Safety Study of Iptacopan in Adult Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH) Using Data From the Non-interventional IPIG PNH Registry

Source: ClinicalTrials.gov · Last updated 23 Jun 2026

Brief summary (registry, in English)

This is an observational single-arm descriptive cohort study based on the secondary use of data collected on iptacopan-treated patients with paroxysmal nocturnal hemoglobinuria (PNH) through the International PNH Interest Group (IPIG) PNH registry.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
200 (estimated)
First submitted
24 Mar 2025
Start date
31 Mar 2025
Primary completion date
1 Oct 2029
Lead sponsor
Novartis Pharmaceuticals
NCT number
NCT06903234

What you commit to

  • Study type: Observational
  • Planned participants: 200
  • From 31 Mar 2025 to the primary completion date, 1 Oct 2029
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Participation in an interventional clinical trial

Who the study is looking for

  • Signed informed consent to participate in the IPIG PNH Registry
  • PNH confirmed by flow cytometry
  • Incident users of iptacopan
  • Aged at least 18 years at the iptacopan initiation

Age in the registry: 18 years to 100 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
-
Coordinator of this site? Confirm its status
BaselSwitzerlandUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.