Study Description
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)
Novartis Investigative Site
Recruiting
Fuchū,Tokyo,1838561,Japan
Novartis Investigative Site
Recruiting
Shinjuku Ku,Tokyo,1628666,Japan
Novartis Investigative Site
Recruiting
Shimajiri-Gun,Okinawa,901-1303,Japan
Novartis Investigative Site
Recruiting
Kitakyushu,Fukuoka,8028555,Japan
Novartis Investigative Site
Recruiting
Nagasaki,Nagasaki,852-8501,Japan
Novartis Investigative Site
Recruiting
Shizuoka,Shizuoka,420-8527,Japan
Novartis Investigative Site
Recruiting
Ishikawa,9208641,Japan
Worldwide Contacts
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