Last Update: Dec 24, 2025
Fabhalta Capsules Specified Drug-use Survey(C3 Glomerulopathy, CLNP023B11401)
ClinicalTrials.gov Identifier:
Novartis Reference Number:CLNP023B11401
All compounds are either investigational or being studied for (a) new use(s). Efficacy and safety have not been established. There is no guarantee that they will become commercially available for the use(s) under investigation.

Study Description

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

C3 Glomerulopathy
Recruiting
50
Sep 17, 2025
Jun 30, 2028
All
0 Years - 100 Years (Child, Adult, Older Adult)

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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Novartis Pharmaceuticals

Novartis Pharmaceuticals

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