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Completed Phase 3 Interventional Accepts healthy volunteers Results available

A Study of Use of Ella®, an Emergency Contraceptive, Under Simulated OTC Conditions

ClinicalTrials.gov ID: NCT03208985

Public ClinicalTrials.gov record NCT03208985. 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 22, 2026, 4:10 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 Multi-Center, Open-Label Trial Investigating Behavior Related to Ella® Use in a Simulated OTC Environment (LIBRella)

Brief summary

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

This study is designed to assess whether consumers select and use ella® (ulipristal acetate 30mg), an emergency contraceptive, in a manner consistent with the OTC package directions in an OTC-like setting.

Study identification

NCT ID
NCT03208985
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
HRA Pharma
Industry
Enrollment
1,270 participants

Conditions and interventions

Eligibility (public fields only)

Age range
Not listed
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
May 23, 2017 (Actual)
Primary completion
Jun 14, 2018 (Actual)
Completion
Jun 14, 2018 (Actual)
Last update posted
Dec 2, 2022

2017 – 2018

United States locations

U.S. sites
34
U.S. states
13
U.S. cities
30
Facility City State ZIP Site status
HRA Pharma Investigational Site Rancho Cucamonga California 91730 —
HRA Pharma Investigational Site Boulder Colorado 80302 —
HRA Pharma Investigational Site Denver Colorado 80003 —
HRA Pharma Investigational Site Denver Colorado 80207 —
HRA Pharma Investigational Site Fort Myers Florida 33919 —
HRA Pharma Investigational Site Miami Florida 33133 —
HRA Pharma Investigational Site Orlando Florida 32817 —
HRA Pharma Investigational Site Pembroke Pines Florida 33026 —
HRA Pharma Investigational Site St. Petersburg Florida 33701 —
HRA Pharma Investigational Site Tampa Florida 33617 —
HRA Pharma Investigational Site Belleville Illinois 62226 —
HRA Pharma Investigational Site Andover Minnesota 55304 —
HRA Pharma Investigational Site Saint Louis Park Minnesota 55426 —
HRA Pharma Investigational Site City of Saint Peters Missouri 63376 —
HRA Pharma Investigational Site Kansas City Missouri 64111 —
HRA Pharma Investigational Site Manchester Missouri 63088 —
HRA Pharma Investigational Site St Louis Missouri 63108 —
HRA Pharma Investigational Site St Louis Missouri 63118 —
HRA Pharma Investigational Site Las Vegas Nevada 89102 —
HRA Pharma Investigational Site Hackensack New Jersey 07601 —
HRA Pharma Investigational Site Morristown New Jersey 07960 —
HRA Pharma Investigational Site New Brunswick New Jersey 08901 —
HRA Pharma Investigational Site Trenton New Jersey 08608 —
HRA Pharma Investigational Site Albuquerque New Mexico 87104 —
HRA Pharma Investigational Site Albuquerque New Mexico 87109 —
HRA Pharma Investigational Site New York New York 10012 —
HRA Pharma Investigational Site Durham North Carolina 27704 —
HRA Pharma Investigational Site Raleigh North Carolina 27603 —
HRA Pharma Investigational Site Portland Oregon 97212 —
HRA Pharma Investigational Site Bremerton Washington 98310 —
HRA Pharma Investigational Site Puyallup Washington 98373 —
HRA Pharma Investigational Site Seattle Washington 98122 —
HRA Pharma Investigational Site Seattle Washington 98133 —
HRA Pharma Investigational Site Tacoma Washington 98405 —

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 NCT03208985, 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 Dec 2, 2022 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03208985 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →