A Multicenter, Postmarketing Study Evaluating the Concentration of Cimzia® in Mature Breast Milk of Lactating Mothers

PHASE1CompletedINTERVENTIONAL
Enrollment

17

Participants

Timeline

Start Date

September 30, 2014

Primary Completion Date

December 31, 2015

Study Completion Date

January 31, 2016

Conditions
Axial Spondyloarthritis (AxSpA)Non-radiographic Evidence-AxSpAAnkylosing SpondylitisCrohn's DiseasePsoriatic ArthritisRheumatoid Arthritis
Interventions
PROCEDURE

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).

BIOLOGICAL

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.

Trial Locations (6)

Unknown

7, Los Angeles

1, Chapel Hill

3, Durham

500, Maastricht

501, Rotterdam

20, Bern

Sponsors
All Listed Sponsors
collaborator

PPD Development, LP

INDUSTRY

collaborator

Parexel

INDUSTRY

lead

UCB BIOSCIENCES, Inc.

INDUSTRY

NCT02154425 - A Multicenter, Postmarketing Study Evaluating the Concentration of Cimzia® in Mature Breast Milk of Lactating Mothers | Biotech Hunter | Biotech Hunter