Danicopan Early Access Program

Study identifier:D7332R00001

ClinicalTrials.gov identifier:NCT05982938

EudraCT identifier:N/A

CTIS identifier:N/A

Recruiting

Official Title

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)

Medical condition

paroxysmal nocturnal hemoglobinuria

Phase

N/A

Healthy volunteers

No

Study drug

Danicopan

Sex

All

Estimated Enrollment

0

Study type

Expanded Access

Age

18 Years - n/a

Date

Study Start Date: -
Primary Completion Date: -
Study Completion Date: -

Study design

Allocation: N/A
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -

Verification:

Verified 01 Dec 2023 by Alexion Pharmaceuticals, Inc.

Sponsors

Alexion Pharmaceuticals, Inc.

Collaborators

-

Inclusion and exclusion criteria