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
Nagoya,Aichi-ken,466-8650,Japan
Novartis Investigative Site
Recruiting
Sapporo,Hokkaido,0040041,Japan
Novartis Investigative Site
Recruiting
Tsu,Mie-ken,514-8507,Japan
Novartis Investigative Site
Recruiting
Takatsuki,Osaka,5698686,Japan
Novartis Investigative Site
Recruiting
Kusatsu,Shiga,525-8585,Japan
Novartis Investigative Site
Recruiting
Ohtsu,Shiga,5202192,Japan
Novartis Investigative Site
Recruiting
Fuchū,Tokyo,1838561,Japan
Novartis Investigative Site
Recruiting
Shinjuku Ku,Tokyo,162 8666,Japan
Novartis Investigative Site
Recruiting
Wakayama,640-8558,Japan
Worldwide Contacts
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