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Clinical trialNCT01467882CompletedPhase 3Interventional

Efficacy, Safety, and Pharmacokinetics (PK) of Triptorelin 6-month Formulation in Patients With Central Precocious Puberty

SponsorDebiopharm International SAEnrollment44Central Precocious Puberty
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The study will investigate the efficacy, safety and pharmacokinetics of triptorelin 22.5 mg 6-month formulation in 44 patients suffering from central precocious puberty. The total study duration per patient will be 12 months (48 weeks).

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

13 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

Chile
  • Idimi

    Santiago, Chile

Mexico
  • Hospital Universitario de Monterrey

    Monterrey, Mexico

United States
  • Pediatric Endocrinology of Phoenix

    Phoenix, Arizona, United States

  • Children'S National Medical Center

    San Diego, California, United States

  • Children'S National Medical Center

    Washington D.C., District of Columbia, United States

  • Arnold Palmer Pediatric Endocrinology Practice

    Orlando, Florida, United States

  • Nancy Wright Md P.A.

    Tallahassee, Florida, United States

  • Washington University

    St Louis, Missouri, United States

  • Hackensack University Medical Center

    Hackensack, New Jersey, United States

  • Women'S & Children'S Hospital of Buffalo

    Buffalo, New York, United States

  • Cincinnati Children'S Hospital

    Cincinnati, Ohio, United States

  • Lynn Health Science Institute

    Oklahoma City, Oklahoma, United States

  • Swedish Pediatric Specialist

    Seattle, Washington, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
30 Apr 2012
Primary completion
31 Aug 2013
Completion
31 Jul 2014
Last update posted
28 Jul 2017
Registered enrollment
44
Registry id
NCT01467882

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.