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NCT06154512Completed

A Real-world, Multi-center, Prospective, Observational Study for PNH in China

A Real-world, Multi-center, Prospective, Observational Study for Paroxysmal Nocturnal Haemoglobinuria (PNH) in China

Source: ClinicalTrials.gov · Last updated 24 Sept 2026

Brief summary (registry, in English)

As a rare disease listed in the First Catalogue of Rare Diseases in China (National Health Commission of the People's Republic of China, 2019), PNH is poorly studied in China subse-quently leading to the inadequate elucidation of disease characteristics and clinical outcomes. Eculizumab was recently approved by NMPA. The availability of Eculizumab in China pro-vides people living with PNH with a new treatment option that can reduce disease symptoms and prevent the dysregulated complement system from causing further damage. A Phase Ⅳ study is necessary to understand the natural history of disease and the clinical outcomes with different medical interventions.

Status (registry)
Completed
Study type
Observational
Enrollment
724 (actual)
First submitted
30 Oct 2023
Start date
10 Nov 2023
Primary completion date
3 Dec 2025
Lead sponsor
AstraZeneca
NCT number
NCT06154512

What you commit to

  • Study type: Observational
  • Participants enrolled: 724
  • From 10 Nov 2023 to the primary completion date, 3 Dec 2025
  • 27 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Current or previous treatment with a non-eculizumab complement inhibitor;

Other

  • Patients in other PNH clinical trials.
  • Unable to give written informed consent.

Who the study is looking for

  • Patients of any age;
  • Diagnosed PNH with detected proportion of PNH clone cells of at least 1%;
  • Patient or patient's family must be willing and able to give written informed consent.

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (27)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
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BeijingChinaUnknown status
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ChangchunChinaUnknown status
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ChangshaChinaUnknown status
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ChengduChinaUnknown status
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GuangzhouChinaUnknown status
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GuiyangChinaUnknown status
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HangzhouChinaUnknown status
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HarbinChinaUnknown status
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HefeiChinaUnknown status
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JinanChinaUnknown status
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KunmingChinaUnknown status
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LinyiChinaUnknown status
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NanchangChinaUnknown status
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NanjingChinaUnknown status
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NanningChinaUnknown status
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NantongChinaUnknown status
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QingdaoChinaUnknown status
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ShanghaiChinaUnknown status
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ShenyangChinaUnknown status
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ShijiazhuangChinaUnknown status
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TaiyuanChinaUnknown status
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TianjinChinaUnknown status
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WuhanChinaUnknown status
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Xi'anChinaUnknown status
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XuzhouChinaUnknown status
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ZhengzhouChinaUnknown status
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ZiboChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.