34
Participants
Start Date
January 24, 2022
Primary Completion Date
September 11, 2023
Study Completion Date
September 11, 2023
Nemolizumab
Participants received either 1 \[30 milligram (mg)\] or 2 (2\*30 mg) subcutaneous (SC) injection(s) of nemolizumab every 4 weeks (Q4W) for a period of 24 weeks (with last injection at Week 20). Participants received the same dosage (1 or 2 SC injections) as received in the lead-in LTE study RD.06.SPR.202699, as assigned by interactive response technology (IRT).
Placebo
Participants received either 1 (30 mg) or 2 (2\*30 mg) SC injection(s) of placebo every 4 weeks for a period of 24 weeks (with last injection at Week 20). Participants received the same dosage (1 or 2 SC injections) as received in the lead-in LTE study RD.06.SPR.202699, as assigned by IRT.
Galderma Investigational Site 5069, Lausanne
Galderma Investigational Site 6158, Vienna
Galderma Investigational Site 5471, Graz
Galderma Investigational Site 5604, Berlin
Galderma Investigational Site 6098, Ansan
Galderma Investigational Site 6168, Valence
Galderma Investigational Site 5104, Brest
Galderma Investigational Site 6082, Bonn
Galderma Investigational Site 8521, Saint Joseph
Galderma Investigational Site 6210, Heidelberg
Galderma Investigational Site 5140, Nice
Galderma Investigational Site 6052, Krakow
Galderma Investigational Site 6237, Ostrowiec Świętokrzyski
Galderma Investigational Site 5495, Rzeszów
Lead Sponsor
Galderma R&D
INDUSTRY