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NCT01535820 · ClinicalTrials.gov registry record · Phase 1

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

A Phase 1 study, sponsored by Johnson & Johnson Pharmaceutical Research & Development, L.L.C..

Completed
Registry status
Phase 1
Development phase
54
Enrollment target

NCT01535820 is a Phase 1 study that has completed, run by Johnson & Johnson Pharmaceutical Research & Development, L.L.C.. The registered enrollment target is 54 participants.

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The verdict

NCT01535820, a Phase 1 study, has completed, sponsored by Johnson & Johnson Pharmaceutical Research & Development, L.L.C..

COMPLETED
Registry status
Phase 1
Development phase
54 participants
Enrollment target

Study Summary

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.

Interventions

  • DRUG Treatment A: ORTHO EVRA patch (NGMN + EE) with an adhesive overlay
  • DRUG Treatment B: ORTHO EVRA patch (NGMN + EE) without an overlay

Trial Details

FieldValue
Enrollment Target 54 participants
Start Date 2011-03
Est. Completion 2011-07
Phase Phase 1

What the Registry Record Tells You About NCT01535820

The ClinicalTrials.gov registry entry for NCT01535820 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 54 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Johnson & Johnson Pharmaceutical Research & Development, L.L.C., which has 102 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Treatment A: ORTHO EVRA patch (NGMN + EE) with an adhesive overlay is the first listed.

NCT01535820 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01535820 about?

NCT01535820 is a clinical study titled "The Effect of an Adhesive Overlay on the Delivery of Contraceptive Hormones From ORTHO EVRA® in Healthy Women". 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.

What is the current status of trial NCT01535820?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 54 participants. The study started on 2011-03. Estimated completion is 2011-07.

What interventions are being tested in trial NCT01535820?

The interventions under investigation include: Treatment A: ORTHO EVRA patch (NGMN + EE) with an adhesive overlay (DRUG), Treatment B: ORTHO EVRA patch (NGMN + EE) without an overlay (DRUG).

Who is sponsoring clinical trial NCT01535820?

This trial is sponsored by Johnson & Johnson Pharmaceutical Research & Development, L.L.C., which has 102 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.