Study identifier:M07-001
ClinicalTrials.gov identifier:NCT01374360
EudraCT identifier:N/A
CTIS identifier:N/A
Paroxysmal Nocturnal hemoglobinuria (PNH) Registry
paroxysmal nocturnal hemoglobinuria
Phase 4
No
-
All
5950
Observational
n/a - n/a
Allocation: Non-randomized
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Feb 2024 by Alexion Pharmaceuticals, Inc.
Alexion Pharmaceuticals, Inc.
-
This study is a collection of data to evaluate safety and characterize progression of Paroxysmal Nocturnal Hemoglobinuria (PNH).
Collection of data to evaluate safety and characterize progression of Paroxysmal Nocturnal Hemoglobinuria (PNH).
Location
Status
Location
Boston, Massachusetts, United States, 02210
Status
Recruiting
Arms | Assigned Interventions |
---|---|
Receiving Soliris or Ultomiris PNH patients of any age, including minors, that are receiving Soliris or Ultomiris | - |
Not receiving Soliris or Ultomiris PNH patients of any age, including minors, that are not receiving Soliris or Ultomiris | - |
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