Study identifier:D7332R00001
ClinicalTrials.gov identifier:NCT05982938
EudraCT identifier:N/A
CTIS identifier:N/A
Early Access Program (EAP) for Danicopan as Add-on Treatment to SOLIRIS® or ULTOMIRIS® in Patients with Paroxysmal Nocturnal Hemoglobinuria (PNH) who have Clinically Significant Extravascular Hemolysis (csEVH)
paroxysmal nocturnal hemoglobinuria
N/A
No
Danicopan
All
0
Expanded Access
18 Years - n/a
Allocation: N/A
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Dec 2023 by Alexion Pharmaceuticals, Inc.
Alexion Pharmaceuticals, Inc.
-
No locations available
Arms | Assigned Interventions |
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