32
Participants
Start Date
August 31, 2016
Primary Completion Date
February 28, 2017
Study Completion Date
February 28, 2017
PR1
"* Active substance: UCB4019~* Route of Administration: subcutaneously"
PL1
"* Active substance: Placebo~* Concentration: 0.9 % saline~* Route of Administration: subcutaneously"
Up0028 001, London
UCB Biopharma S.P.R.L.
INDUSTRY