The main objective of this study is to evaluate the efficacy of danicopan as add-on
therapy to a complement component 5 (C5) inhibitor (eculizumab or ravulizumab) in
participants with PNH who have clinically evident EVH.
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT04469465.
Locations matching your search criteria
United States
North Carolina
Durham
Duke University Medical CenterStatus: Active
Name Not Available
This is a multiple-region, randomized, double-blind, placebo controlled, multiple-dose,
study in participants with PNH who have clinically evident EVH on a C5 inhibitor
(eculizumab or ravulizumab).
Participants will be randomized to receive danicopan or placebo, in a 2:1 ratio for 12
weeks (Treatment Period 1) in addition to their C5 inhibitor (eculizumab or ravulizumab)
therapy. At Week 12, participants randomized to receive placebo will be switched to
danicopan in addition to their C5 inhibitor for an additional 12 weeks (Treatment Period
2) and participants randomized to danicopan will continue on danicopan for an additional
12 weeks, while remaining on their ongoing C5 inhibitor therapy.
At the end of the 2 treatment periods (Week 24), participants may enter a Long-Term
Extension (LTE) Period and continue to receive danicopan in addition to their C5
inhibitor therapy. The Long-Term Extension period will consist of a first year of
LTE(Year1) and a second year of optional LTE(Year2).All patients will complete 72 weeks
of LTE(Year 1) assessments. After Week 72 (at the end of the first year of LTE), patients
have the choice to complete participation in this study or continue to the optional
second year (Year2) of LTE.
Lead OrganizationAlexion Pharmaceuticals Inc