17
Participants
Start Date
September 30, 2014
Primary Completion Date
December 31, 2015
Study Completion Date
January 31, 2016
Breast milk sampling
Pharmacokinetic (PK) samples will be taken from breast milk of lactating mothers on an established dosing regimen of CZP on Day 0 of the Sampling Period, just prior to next scheduled dose of CZP, and on Days 2, 4, 6, 8, 10, 12, and 14 (pre-dose for mothers on CZP Q2W), relative to CZP administration on Day 0. In addition, in mothers on a CZP Q4W dosing regimen, the concentration of CZP in breast milk will also be evaluated on or about Day 28 (i.e., prior to and on the same day of the next scheduled administration of CZP).
Certolizumab Pegol
Mothers who decided to continue on, or to start treatment with, Certolizumab Pegol (CZP) for an approved indication with their treating physician prior to participation into this study. The mother is responsible for procuring her own supply of commercial CZP. The CZP dose and administration schedule will be as per the locally approved label.
7, Los Angeles
1, Chapel Hill
3, Durham
500, Maastricht
501, Rotterdam
20, Bern
Collaborators (2)
PPD Development, LP
INDUSTRY
Parexel
INDUSTRY
UCB BIOSCIENCES, Inc.
INDUSTRY