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Study of Efficacy and Safety of Iptacopan in Patients With C3 Glomerulopathy.

NCT04817618

This study is recruiting at 5 US sites in 4 states, according to its ClinicalTrials.gov record last updated .

Summary

The Primary Completion Date and Study Completion Date have been updated to reflect completion of the adolescent cohort, which has been added to the protocol. The study is designed as a multicenter, randomized, double-blind, parallel group, placebo-controlled study to evaluate the efficacy and safety of iptacopan (LNP023) in complement 3 glomerulopathy.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • C3G

Eligibility basics and study details

Study type
Interventional
Phase
Phase 3
Ages
12 to 60 years
Sex
All
Healthy volunteers
Not accepted
Sponsor
Novartis Pharmaceuticals
Last updated on ClinicalTrials.gov
July 13, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

Colorado · 1

  • Childrens Hospital Colorado · Aurora, CO

Florida · 1

  • Nicklaus Childrens Hospital · Miami, FL

Iowa · 2

  • University of Iowa Health Care · Iowa City, IA
  • University of Iowa Health Care · Iowa City, IA

Wisconsin · 1

  • University of Wisconsin · Madison, WI

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.