Long Beach, California 90806


Purpose:

The primary objective of the study is to assess the safety and efficacy of a leuprolide acetate (LA) 45 mg 6-month depot formulation for the treatment of CPP in children who are either naïve to treatment with a gonadotropin-releasing hormone agonist (GnRHa) or who have been previously treated with a GnRHa.


Criteria:

Inclusion Criteria: - Children with CPP who are naïve to treatment with a gonadotropin-releasing hormone agonist (GnRHa) (females 2 - 8 years of age, or males 2 - 9 years of age) or who have been on standard GnRHa therapy for at least 6 months (females 2 - 10 years of age, or males 2 - 11 years of age). - No history of clinically significant medical conditions or any other reason that the investigator determines would make the participant an unsuitable candidate to receive study drug. Exclusion Criteria:


NCT ID:

NCT03695237


Primary Contact:

Study Director
AbbVie Inc.
AbbVie

ABBVIE CALL CENTER
Phone: 847.283.8955
Email: abbvieclinicaltrials@abbvie.com


Backup Contact:

N/A


Location Contact:

Long Beach, California 90806
United States



There is no listed contact information for this specific location.

Site Status: Recruiting


Data Source: ClinicalTrials.gov

Date Processed: February 04, 2019

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