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Active Not Recruiting NCT07156149

Fabhalta Capsules Specified Drug-use Survey

Conditions: C3 Glomerulopathy

Sex: All
Ages: 0 Years – 100 Years
Healthy volunteers: No
Enrollment: 32
Sponsor: Novartis Pharmaceuticals

Location: Novartis Investigative Site Nagoya Aichi-ken

Summary

The objective of this study is to evaluate the safety and effectiveness of Fabhalta in patients with C3 glomerulopathy in clinical practice.

Eligibility Criteria

Inclusion Criteria: * All patients who have used Fabhalta for C3 glomerulopathy (including patients with recurrent C3 glomerulopathy post renal transplant). Exclusion Criteria: * Use of iptacopan for an indication not yet approved under the Clinical Trials Act or GCP (e.g., patient-requested medical treatment, investigator-initiated clinical trial)

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07156149). StuddyBuddy aggregates publicly available trial information.