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NCT01077505

An Evaluation of the Pharmacokinetics of an Oral Contraceptive (Brevicon) When Co-administered With Albiglutide .

Completed Phase 1 Last updated 14 June 2017
What this trial tests

Phase 1 trial testing albiglutide in Diabetes Mellitus, Type 2 in 16 participants. Completed in 24 November 2010.

Timeline
15 March 2010
Primary endpoint
24 November 2010
24 November 2010

Quick facts

Lead sponsorGlaxoSmithKline
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designsingle group
Maskingnone
Primary purposeother
Enrollment16
Start date15 March 2010
Primary completion24 November 2010
Estimated completion24 November 2010
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

GlaxoSmithKline — full company profile →

Who can join

Adults 18 to 40, female only, with Diabetes Mellitus, Type 2. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study will be an open-label study to evaluate the effect of albiglutide on the pharmacokinetics and pharmacodynamics of a standard oral contraceptive regimen (Brevicon). The primary objective of this study is to demonstrate the lack of effect of albiglutide doses on the pharmacokinetics of norethindrone and ethinyl estradiol in healthy female subjects.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Clinical pharmacology of albiglutide, a GLP-1 receptor agonist.
    Young MA, Wald JA, Matthews JE, Scott R, et al · · 2014 · cited 28× · PMID 25387217 · DOI 10.3810/pgm.2014.11.2836

Verify or expand the search:

Other trials of albiglutide

Trials testing the same drug.

Other recruiting trials for Diabetes Mellitus, Type 2

Currently open trials in the same condition.

Other GlaxoSmithKline trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01077505.

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