The Effect of an Adhesive Overlay on the Delivery of Contraceptive Hormones From ORTHO EVRA® in Healthy Women

Completed · Phase 1

Conditions studied: Healthy Volunteers

In brief

The purpose of this study is to assess the bioequivalence of the contraceptive hormones of ORTHO EVRA when the patch is applied with and without an adhesive overlay.

Key facts

Study ID
NCT01535820
Run by
Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
People needed
54
Starts
2011-03-01
Expected to finish
2011-07-01
Last updated by the study team
2013-03-20

Who can join

Age: 18 and older, up to 45. Sex: female. Healthy volunteers: accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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