Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 3 Interventional Accepts healthy volunteers Results available

A Study to Evaluate the Efficacy and Safety of DR-102 for the Prevention of Pregnancy

ClinicalTrials.gov ID: NCT01178125

Public ClinicalTrials.gov record NCT01178125. 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, 6:24 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 Multicenter, Open-Label Study to Evaluate the Efficacy and Safety of a Combination Oral Contraceptive Regimen (DR-102) for the Prevention of Pregnancy in Women

Brief summary

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

This is an open-label, single treatment study. All subjects will receive 12 months of oral contraceptive therapy with DR-102. Study participants will receive physical and gynecological exams, including Pap smear. During the study, all participants will be required to complete a daily diary.

Study identification

NCT ID
NCT01178125
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
2,858 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 40 Years
Sex
Female
Healthy volunteers
Accepts healthy volunteers

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

Study timeline

Start date
Aug 2010 (Type not available)
Primary completion
Jan 2013 (Actual)
Completion
Jan 2013 (Actual)
Last update posted
Nov 9, 2021

2010 – 2013

United States locations

U.S. sites
52
U.S. states
21
U.S. cities
45
Facility City State ZIP Site status
Teva Investigational Site 10007 Montgomery Alabama — —
Teva Investigational Site 10013 Phoenix Arizona — —
Teva Investigational Site 10017 Phoenix Arizona — —
Teva Investigational Site 10032 Little Rock Arkansas — —
Teva Investigational Site 10026 San Diego California — —
Teva Investigational Site 10056 San Diego California — —
Teva Investigational Site 10002 Colorado Springs Colorado — —
Teva Investigational Site 10033 Colorado Springs Colorado — —
Teva Investigational Site 10057 Washington D.C. District of Columbia — —
Teva Investigational Site 10052 Clearwater Florida — —
Teva Investigational Site 10021 Jacksonville Florida — —
Teva Investigational Site 10036 Leesburg Florida — —
Teva Investigational Site 10012 Miami Florida — —
Teva Investigational Site 10015 Miami Florida — —
Teva Investigational Site 10055 Palm Beach Gardens Florida — —
Teva Investigational Site 10001 West Palm Beach Florida — —
Teva Investigational Site 10031 Decatur Georgia — —
Teva Investigational Site 10041 Roswell Georgia — —
Teva Investigational Site 10050 Savannah Georgia — —
Teva Investigational Site 10008 Louisville Kentucky — —
Teva Investigational Site 10023 Mount Sterling Kentucky — —
Teva Investigational Site 10048 Lawrenceville New Jersey — —
Teva Investigational Site 10030 Moorestown New Jersey — —
Teva Investigational Site 10014 Albuquerque New Mexico — —
Teva Investigational Site 10006 Rochester New York — —
Teva Investigational Site 10044 Cary North Carolina — —
Teva Investigational Site 10040 Charlotte North Carolina — —
Teva Investigational Site 10034 New Bern North Carolina — —
Teva Investigational Site 10018 Winston-Salem North Carolina — —
Teva Investigational Site 10046 Winston-Salem North Carolina — —
Teva Investigational Site 10022 Columbus Ohio — —
Teva Investigational Site 10039 Columbus Ohio — —
Teva Investigational Site 10028 Oklahoma City Oklahoma — —
Teva Investigational Site 10043 Philadelphia Pennsylvania — —
Teva Investigational Site 10003 Pittsburgh Pennsylvania — —
Teva Investigational Site 10049 Bluffton South Carolina — —
Teva Investigational Site 10037 Columbia South Carolina — —
Teva Investigational Site 10035 Greenville South Carolina — —
Teva Investigational Site 10047 Mt. Pleasant South Carolina — —
Teva Investigational Site 10016 Jackson Tennessee — —
Teva Investigational Site 10045 Knoxville Tennessee — —
Teva Investigational Site 10005 Memphis Tennessee — —
Teva Investigational Site 10042 Nashville Tennessee — —
Teva Investigational Site 10054 Dallas Texas — —
Teva Investigational Site 10019 Houston Texas — —
Teva Investigational Site 10020 San Antonio Texas — —
Teva Investigational Site 10038 Arlington Virginia — —
Teva Investigational Site 10024 Norfolk Virginia — —
Teva Investigational Site 10051 Norfolk Virginia — —
Teva Investigational Site 10053 Richmond Virginia — —
Teva Investigational Site 10027 Seattle Washington — —
Teva Investigational Site 10029 Tacoma Washington — —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 10 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01178125, 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 Nov 9, 2021 · Synced Oct 21, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01178125 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →