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NCT00411684 · ClinicalTrials.gov registry record · Phase 3

Safety and Efficacy of CDB-2914 for Emergency Contraception

A Phase 3 study of Emergency Contraception, sponsored by HRA Pharma.

Completed
Registry status
Phase 3
Development phase
1,623
Enrollment target
17
Study locations

NCT00411684: Completed Phase 3 study of Emergency Contraception, sponsored by HRA Pharma.

NCT00411684 is a Phase 3 study of Emergency Contraception that has completed, run by HRA Pharma. The registered enrollment target is 1,623 participants, above the 1,164-participant average among 3 other Emergency Contraception trials with a reported enrollment target (39% higher). The trial reports 17 study locations across 15 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00411684, a Phase 3 study of Emergency Contraception, has completed, sponsored by HRA Pharma.

COMPLETED
Registry status
Phase 3
Development phase
1,623 participants
Enrollment target
17
Study locations

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.

Primary Outcome

A high sensitivity pregnancy test was performed at inclusion (between 48h and 120h after unprotected intercourse) and then until menses occured or up to 60 days if they did not, at the following time points: * 5-7 days after expected date of menses * 1 week later * every two week after

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

FieldValue
Enrollment Target 1,623 participants
Start Date 2006-11
Est. Completion 2009-06-05
Phase Phase 3
HRA Pharma

9 total trials

What the finished NCT00411684 record still lists

NCT00411684 is an interventional study that assigns participants to a tested intervention. Its 1,623 participants enrollment target places it among the larger protocols in the corpus, above the 1,164-participant average among 3 other Emergency Contraception trials with a reported enrollment target (39% higher).

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.

NCT00411684 lists 17 locations in 15 states (Florida, Texas, California).

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.

What interventions are being tested in trial NCT00411684?

The interventions under investigation include: CDB-2914 (DRUG).

Who is sponsoring clinical trial NCT00411684?

This trial is sponsored by HRA Pharma, which has 9 total clinical trials registered on ClinicalTrials.gov.

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.

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Source: ClinicalTrials.gov NCT00411684, the US trial registry maintained by the National Library of Medicine. NCT00411684 (large enrollment · multi site footprint · completed) retrieved and formatted by PlainTrial, see methodology.