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Active, not recruiting Phase 3 Interventional

Study to Evaluate Contraceptive Efficacy and Safety of a Progestin Only Patch in Women of Childbearing Potential

ClinicalTrials.gov ID: NCT06672016

Public ClinicalTrials.gov record NCT06672016. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 2:38 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3, Multicenter, Open-Label, Single-Arm Study of MR-130A-01 in Women of Childbearing Potential to Evaluate Contraceptive Efficacy and Safety

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The Sponsor is developing a progestin-only contraceptive transdermal system (patch). The main purpose of this study is to look at how safe the study patch is and how well it works in preventing pregnancy. The study will also look at how well the study patch is tolerated. The study patch is a transdermal system that contains the active ingredient, progestin.

Study identification

NCT ID
NCT06672016
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Mylan Pharmaceuticals Inc
Industry
Enrollment
1,630 participants

Conditions and interventions

Eligibility (public fields only)

Age range
16 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 13, 2025 (Actual)
Primary completion
May 2027 (Estimated)
Completion
May 2027 (Estimated)
Last update posted
Oct 13, 2026

2025 – 2027

United States locations

U.S. sites
56
U.S. states
22
U.S. cities
43
Facility City State ZIP Site status
Alabama Clinical Therapeutics, LLC Birmingham Alabama 35235 —
SEC Clinical Research Dothan Alabama 36305 —
AMR Mobile Mobile Alabama 36608 —
Velocity Clinical Research Mobile Alabama 36608 —
Velocity Clinical Research Phoenix Arizona 85006 —
Precision Trials Phoenix Arizona 85032 —
Velocity Clinical Research Santa Ana Huntington Park California 90255 —
Essential Access Health Los Angeles California 90017 —
Women's Health Care Research Corp San Diego California 92111 —
WR-Medical Center For Clinical Research San Diego California 92120 —
Altus Research Lake Worth Florida 33461 —
OB GYN Associates of Mid Florida P.A. Leesburg Florida 34748 —
Genoma Research Group Miami Florida 33173 —
Spotlight Research Center Miami Florida 33176 —
New Age Med Research Corp Miami Florida 33186 —
Sensible Healthcare, LLC Ocoee Florida 34761 —
Innovation Medical Research Center Palmetto Bay Florida 33157 —
Clinical Research Center of Florida Pompano Beach Florida 33060 —
CenExel iResearch LLC Decatur Georgia 30030 —
CenExel Savannah Savannah Georgia 31405 —
Javarra and Privia Med Savannah Georgia 31406 —
Leavitt ClinResearch Idaho Falls Idaho 83404 —
Women's Healthcare Associates P.A. Idaho Falls Idaho 83404 —
AMR Newton Newton Kansas 67114 —
AMR Lexington Lexington Kentucky 40509 —
Clinical Trials Management, LLC Covington Louisiana 70433 —
Velocity Clinical Research Covington Louisiana 70433 —
Velocity Clinical Research Lafayette Louisiana 70508 —
PraetorianPharmaResearch LLC Marrero Louisiana 70072 —
Southern Clinical Research Associates Metairie Louisiana 70001 —
Velocity Clinical Research New Orleans New Orleans Louisiana 70119 —
Valley OBGYN Clinic PC Saginaw Michigan 48602 —
Velocity Clinical Research Gulfport Mississippi 39503 —
Alliance for Multispecialty Research Kansas City Missouri 64114 —
M3 Wake Research Inc Las Vegas Nevada 89106 —
Excel Clinical Research Las Vegas Nevada 89109 —
Essential Women's Health Las Vegas Nevada 89113 —
CenExel Hassman Research Institute Marlton New Jersey 08053 —
Albuquerque Clinic Trials Inc Albuquerque New Mexico 87102 —
Bosque Women's Care Albuquerque New Mexico 87109 —
M3 Wake Research, Inc. Raleigh North Carolina 27612 —
Velocity Clinical Research Beachwood Ohio 44122 —
Clinical Research Philadelphia Philadelphia Pennsylvania 19114 —
Cedar Health Research, LLC Euless Texas 76040 —
Helios Clinical Research Fort Worth Texas 76104 —
ACRC Trials Frisco Texas 75033 —
Javara Houston Texas 77054 —
Clinical Trial Network LLC Houston Texas 77074 —
Javara Rowlett Texas 75088 —
Stephenville Medical and Surgical Clinic Stephenville Texas 76401 —
Javara Sugarland Texas 77478 —
Helios Clinical Research Weatherford Texas 76086 —
Wasatch Clinical Research Salt Lake City Utah 84102 —
Tidewater Clinical Research Norfolk Virginia 23052 —
AMR Norfolk Norfolk Virginia 23502 —
Seattle Clinical Research Center Seattle Washington 98104 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06672016, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 13, 2026 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06672016 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →