32
Participants
Start Date
October 28, 2015
Primary Completion Date
July 9, 2018
Study Completion Date
October 11, 2018
BAY1093884
Single escalating dose with a starting dose of 0.3 mg/kg for the first cohort. Drug will be administered via IV infusion over 1 hour and SC injection. Based on safety, PK and PD results the doses for the other cohorts will be determined.
BAY1093884
Multiple dose cohort with a single 150-mg SC injection once a week for 6 weeks.
Sofia
Plovdiv
Varna
Berlin
Giessen
Lviv
Suginami
Kiev
London
Manchester
Lead Sponsor
Bayer
INDUSTRY