Lack of placental transfer of certolizumab pegol during pregnancy: results from CRIB, a prospective, postmarketing, pharmacokinetic study

…, RM Flipo, A Van Tubergen, L Shaughnessy… - Annals of the …, 2018 - ard.bmj.com
Objectives There is a need for effective and safe treatment during pregnancy in women with
chronic inflammatory diseases. This study evaluated placental transfer of certolizumab pegol …

Minimal to no transfer of certolizumab pegol into breast milk: results from CRADLE, a prospective, postmarketing, multicentre, pharmacokinetic study

…, A Van Tubergen, L Shaughnessy… - Annals of the …, 2017 - ard.bmj.com
Background Women with chronic inflammatory diseases face uncertainty regarding the
safety of biologics during breast feeding. CRADLE was the first industry-sponsored study to …

[PDF][PDF] Pregnancy outcomes after exposure to certolizumab pegol: updated results from a pharmacovigilance safety database

…, JJ Cush, M Cooney, L Shaughnessy… - Arthritis & …, 2018 - Wiley Online Library
Objective Anti–tumor necrosis factor (anti‐ TNF ) medications are effective in controlling chronic
inflammatory diseases, but information about their use and safety in pregnancy is limited…

Pregnancy outcomes in subjects exposed to certolizumab pegol

…, JJ Cush, A Golembesky, L Shaughnessy… - The Journal of …, 2015 - jrheum.org
Objective. To provide information on pregnancy outcomes in women receiving certolizumab
pegol (CZP). Methods. The UCB Pharma safety database was searched for pregnancies …

Long-term safety and efficacy of certolizumab pegol in combination with methotrexate in the treatment of rheumatoid arthritis: 5-year results from the RAPID 1 trial and …

…, V Strand, P Mease, L Shaughnessy… - Annals of the …, 2014 - ard.bmj.com
Objectives To examine the safety and efficacy of 5-year administration of certolizumab
pegol (CZP)+methotrexate (MTX) in patients with active rheumatoid arthritis (RA). Methods …

Ghrelin agonist (TZP‐101): safety, pharmacokinetics and pharmacodynamic evaluation in healthy volunteers: a phase I, first‐in‐human study

KC Lasseter, L Shaughnessy… - The Journal of …, 2008 - Wiley Online Library
The authors evaluate the human safety, tolerability, pharmacokinetics, and pharmacodynamics
of TZP‐101, an agonist of the hGHS‐R1a (ghrelin) receptor. Healthy subjects were …

Time course of changes in cholinergic and neurotrophin-related markers after infusion of colchicine into the basal forebrain

LW Shaughnessy, WR Mundy, HA Tilson, S Barone Jr - Brain research, 1998 - Elsevier
After bilateral infusions of colchicine or vehicle in the rat nucleus basalis magnocellularis,
the time course of changes in several cholinergic and neurotrophin-related markers were …

Contribution of protein binding to the pharmacokinetics of the ghrelin receptor agonist TZP-101 in healthy volunteers and adults with symptomatic gastroparesis: two …

…, N Ejskjaer, M Gutierrez, L Shaughnessy… - Clinical drug …, 2009 - Springer
Background and objective: TZP-101 is a selective, small molecule ghrelin receptor agonist
in clinical development for the treatment of gastric motility disorders. The objectives of this …

Novel approaches to models of Alzheimer's disease pathology for drug screening and development

L Shaughnessy, B Chamblin, L McMahon… - Journal of Molecular …, 2004 - Springer
Abstract Development of therapeutics for Alzheimer’s disease (AD) requires appropriate cell
culture models that reflect the errant biochemical pathways and animal models that reflect …

Comparison of intracranial infusions of colchirine and ibotenic acid as models of neurodegeneration in the basal forebrain

LW Shaughnessy, S Barone Jr, WR Mundy, DW Herr… - Brain research, 1994 - Elsevier
Colchicine and ibotenic acid were compared for their ability to produce neurodegeneration
and cognitive deficit after bilateral infusions into the nucleus basalis magnocellularis of male …