Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
Safety and Efficacy of CDB-2914 for Emergency Contraception
NCT00411684 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to assess the safety and efficacy of CDB-2914 for preventing pregnancy when taken 3 to 5 days after unprotected sexual intercourse.
Conditions Studied
Interventions
- DRUG CDB-2914
Study Locations (17)
Florida
- Planned Parenthood of Greater Miami, Palm Beach and Treasure Cost — Miami
- Planned Parenthood of South Palm Beach, Pembroke Pines — Pembroke Pines
Texas
- Planned Parenthood of the Texas Capital Region — Austin
- Planned Parenthood of Houston and Southeast Texas — Houston
California
- Planned Parenthood of Mar Monte — San Jose
Colorado
- Planned Parenthood of the Rocky Mountains — Denver
Indiana
- Planned Parenthood of Indiana — Bloomington
Iowa
- Planned Parenthood of Greater Iowa — Ames
Maryland
- Planned Parenthood of Maryland — Baltimore
Massachusetts
- Planned Parenthood League of Massachusetts — Boston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,623 participants |
| Start Date | 2006-11 |
| Est. Completion | 2009-06-05 |
| Phase | Phase 3 |
Interested in This Trial?
Always speak with your doctor before enrolling in a clinical trial.
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00411684
The ClinicalTrials.gov registry entry for NCT00411684 describes a study currently listed as completed. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 1,623 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is HRA Pharma, which has 3 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Emergency Contraception appearing as the primary indexed condition, and to 1 intervention — of which CDB-2914 is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT00411684 reports 17 study locations spanning 15 distinct geographic areas — top geographies include Florida, Texas, California. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT00411684 about?
NCT00411684 is a clinical study titled "Safety and Efficacy of CDB-2914 for Emergency Contraception". The purpose of this study is to assess the safety and efficacy of CDB-2914 for preventing pregnancy when taken 3 to 5 days after unprotected sexual intercourse.
What is the current status of trial NCT00411684?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 1,623 participants. The study started on 2006-11. Estimated completion is 2009-06-05.
What conditions does trial NCT00411684 study?
This clinical trial studies the following conditions: Emergency Contraception. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00411684?
The interventions under investigation include: CDB-2914 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00411684?
This trial is sponsored by HRA Pharma, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00411684 being conducted?
This trial has 17 study locations across California, Colorado, Florida, Indiana, Iowa. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
How Clinical Trials Work
Understand phases 1-4, trial design, randomization, and the informed consent process.
Patient Rights in Clinical Trials
Your rights as a participant: consent, withdrawal, privacy, and who to contact.
Finding the Right Clinical Trial
A practical guide to searching trials, understanding eligibility, and evaluating options.
All Guides
Browse our complete library of clinical trial educational resources.
Read our methodology — how this data is sourced, computed, and verified.