Condition: Paroxysmal Nocturnal Hemoglobinuria · C3 Glomerulopathy · Sponsor: Novartis Pharmaceuticals
This is a post-marketing surveillance study conducted as part of the Risk Management Plan (RMP) for South Korea, to evaluate the safety and effectiveness of iptacopan in real-world clinical settings for the treatment of either PNH or C3G in Korean patients. Prospective data will be collected from patient medical records to address the objectives for all eligible populations.
This description comes directly from the study's public registry record.
Novartis Pharmaceuticals · +41613241111 · novartis.email@novartis.com
Novartis Pharmaceuticals
Always discuss trial participation with your own doctor first.
| Novartis Investigative Site | Jeollanam, South Korea | Recruiting |
| Novartis Investigative Site | Seoul, South Korea | Recruiting |
| Novartis Investigative Site | Seoul, South Korea | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07416162