A Study of Leuprolide 11.25 mg and 30 mg Administered Every 3 Months to Treat Central Precocious Puberty
Public ClinicalTrials.gov record NCT00635817. 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.
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, Randomized, Multi-Center, Open-Label Study to Evaluate the Efficacy and Safety of Leuprolide Acetate 11.25 and 30 mg Formulations in Children With Central Precocious Puberty
Study identification
- NCT ID
- NCT00635817
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Phase 3
- Lead sponsor
- Abbott
- Industry
- Enrollment
- 84 participants
Conditions and interventions
Conditions
Interventions
- Leuprolide acetate 11.25 mg Drug
- Leuprolide acetate 30 mg Drug
Drug
Eligibility (public fields only)
- Age range
- 2 Years to 11 Years
- Sex
- All
- 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
- May 31, 2008
- Primary completion
- Dec 31, 2009
- Completion
- May 31, 2010
- Last update posted
- Nov 1, 2011
2008 – 2010
United States locations
- U.S. sites
- 21
- U.S. states
- 12
- U.S. cities
- 19
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Site Reference ID/Investigator# 8765 | Birmingham | Alabama | 35233 | — |
| Site Reference ID/Investigator# 11522 | Long Beach | California | 90806 | — |
| Site Reference ID/Investigator# 8756 | Los Angeles | California | 90027 | — |
| Site Reference ID/Investigator# 8755 | San Diego | California | 92123 | — |
| Site Reference ID/Investigator# 8761 | San Diego | California | 92123 | — |
| Site Reference ID/Investigator# 8772 | Stanford | California | 94305-5208 | — |
| Site Reference ID/Investigator# 8749 | Greenwood Village | Colorado | 80111 | — |
| Site Reference ID/Investigator# 8771 | Gainesville | Florida | 32608 | — |
| Site Reference ID/Investigator# 8764 | Jacksonville | Florida | 32207 | — |
| Site Reference ID/Investigator# 17621 | Pensacola | Florida | 32504 | — |
| Site Reference ID/Investigator# 8752 | Indianapolis | Indiana | 46202 | — |
| Site Reference ID/Investigator# 8766 | Shreveport | Louisiana | 71103 | — |
| Site Reference ID/Investigator# 8768 | Minneapolis | Minnesota | 55455 | — |
| Site Reference ID/Investigator# 17341 | Saint Paul | Minnesota | 55102 | — |
| Site Reference ID/Investigator# 8759 | Kansas City | Missouri | 64108 | — |
| Site Reference ID/Investigator# 8750 | Oklahoma City | Oklahoma | 73104 | — |
| Site Reference ID/Investigator# 8760 | Tulsa | Oklahoma | 74135 | — |
| Site Reference ID/Investigator# 8763 | Hershey | Pennsylvania | 17033 | — |
| Site Reference ID/Investigator# 8754 | Salt Lake City | Utah | 84108 | — |
| Site Reference ID/Investigator# 8762 | Seattle | Washington | 98104 | — |
| Site Reference ID/Investigator# 8753 | Seattle | Washington | 98105 | — |
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 4 non-U.S. sites.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT00635817, 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 1, 2011 · Synced May 20, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT00635817 live on ClinicalTrials.gov.