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Study identifier: NCT06931691 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Multi-center, Ambispective Cohort Study to Evaluate the Impact of Iptacopan for Adult Patients With PNH in China

Condition: Paroxysmal Nocturnal Hemoglobinuria  ·  Sponsor: Novartis Pharmaceuticals

PhaseN/A
Planned participants80
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNo

About this study

The implementation of new standards for the management of PNH and the use of iptacopan in patients with PNH are expected to change the treatment landscape and improve the overall prognosis of patients. Based on these backgrounds, we plan to conduct a real-world study of iptacopan to further evaluate its impact on treatment-related outcomes, disease management, and healthcare resource utilization in Chinese patients with PNH.

This description comes directly from the study's public registry record.

Talk to the study team

Novartis Pharmaceuticals  ·  +41613241111  ·  novartis.email@novartis.com

Novartis Pharmaceuticals

Always discuss trial participation with your own doctor first.

Locations (14)

Novartis Investigative SiteHefei, Anhui, ChinaRecruiting
Novartis Investigative SiteGuangzhou, Guangdong, ChinaRecruiting
Novartis Investigative SiteGuangzhou, Guangdong, ChinaRecruiting
Novartis Investigative SiteShijiazhuang, Hebei, ChinaRecruiting
Novartis Investigative SiteZhengzhou, Henan, ChinaRecruiting
Novartis Investigative SiteZhengzhou, Henan, ChinaRecruiting
Novartis Investigative SiteWuhan, Hubei, ChinaRecruiting
Novartis Investigative SiteNantong, Jiangsu, ChinaRecruiting
Novartis Investigative SiteNanchang, Jiangxi, ChinaRecruiting
Novartis Investigative SiteChangchun, Jilin, ChinaRecruiting
Novartis Investigative SiteJinan, ChinaRecruiting
Novartis Investigative SiteTianjin, ChinaRecruiting

+ 2 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06931691