LivingGLP1
Study S002216

An Open-label Study to Evaluate the Pharmacokinetics of an Oral Contraceptive Containing Norethindrone and Ethinyl Estradiol When Co-administered With GSK716155 in Healthy Adult Female Subjects

Registration

Registration
NCT01077505
Study type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Phase
PHASE1
Masking
NONE
Status
COMPLETED
Enrollment
16
Start
2010-03-15
Primary completion
2010-11-24
Lead sponsor
GlaxoSmithKline
Conditions
Diabetes Mellitus, Type 2
Interventions
BIOLOGICAL:albiglutide; DRUG:Oral contraceptive (Brevicon)
Results posted
FALSE
Individual participant data sharing
YES

Registered primary outcomes

  • AUC0-24 of norethindrone and ethinyl estradiol after OC alone in Period 1 and after OC with albiglutide in Period 2. [Day 21]

Linked records (2)

Automatic links, confirmed or rejected during screening. A record citing this registration may be a secondary analysis, a commentary or a review that mentions the trial.
RecordTitleYearDesignIdentifiersLink basis
R0018591Clinical pharmacology of albiglutide, a GLP-1 receptor agonist.
Young MA, Postgraduate medicine
2014Other trialPMID 25387217DOIcites ClinicalTrials.gov:NCT01077505; registry reference DERIVED:25387217
R0022625Effects of multiple doses of albiglutide on the pharmacokinetics, pharmacodynamics, and safety of digoxin, warfarin, or a low-dose oral contraceptive.
Bush M, Postgraduate medicine
2012Other trialPMID 23322139DOIregistry reference BACKGROUND:23322139