Iptacopan for Adult C3 Glomerulopathy in Spain
Official title: Clinical Experience With Iptacopan in Adult Patients With Complement 3 Glomerulopathy (C3G): A Multicenter, Observational, Retrospective Study of Patients Treated Through an Early Access Program in Spain
Run by Novartis · NCT07598448 · Data updated 2026-11-12
This is an observational program in Spain looking at adults with C3G who have received iptacopan through an early access program to see real-world experiences.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 100 Years |
| Sex | All |
| Enrollment | 35 (estimated) |
| Sponsor | Novartis Industry-sponsored |
| Locations | 2 sites (Córdoba and 1 other locations) |
| Status | Recruiting |
| Started | September 22, 2026 |
| Main results expected | December 15, 2026 |
| Study ends | December 15, 2026 |
| Registry record updated | October 7, 2026 |
| Trial ID | NCT07598448 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults (18 years or older) with biopsy-confirmed C3G who received at least one dose of iptacopan through the Spanish EAP between 2020 and 2025.
✕Probably not a fit
Patients who did not respond to iptacopan or who were treated for non-C3G indications would be less likely to benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study characterizes patient profiles and clinical experiences of iptacopan treatment in adult C3G patients who were given access through a Spain-based early access program between 2020 and 2025. It focuses on real-world use, including dosing and outcomes, in routine clinical settings. No formal comparative or interventional endpoints are specified in the description. Data are collected from multiple Spanish investigational sites affiliated with Novartis.
Why it matters
Potential benefit: If successful, findings could inform future treatment approaches with iptacopan for C3G and help guide clinicians on real-world use and patient selection.
How similar studies have gone: Observational experiences with iptacopan and complement pathway inhibitors have shown practical insights in real-world settings, though this program represents a limited, non-randomized context.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion criteria: 1. Adult patients (≥18 years). 2. Biopsy-confirmed C3G. 3. Patients who have received at least one dose of iptacopan through an EAP from October 2020 to June 2025. Exclusion criteria: 1\. Patients treated with iptacopan through an EAP for indications other than C3G.
Where it's running
-
Novartis Investigative Site
Córdoba, Spain Recruiting -
Novartis Investigative Site
Madrid, Spain Recruiting
Study contacts
- Study coordinator: Novartis Pharmaceuticals
- Email: novartis.email@novartis.com
- Phone: +41613241111
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.