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Updated: Aug 14, 2026

In Vitro Imaging and Quantification of the Drug Targeting Efficiency of Fluorescently Labeled GnRH Analogues
Published on: March 21, 2017
[Treatment of precocious puberty by GnRH agonists]
1Endocrinologie pédiatrique & INSERM U561, groupe hospitalier Cochin-Saint-Vincent-de-Paul, 82, avenue Denfert-Rochereau, 75674 Paris 14, France.
Abstract:
The objective of GnRH agonist treatment in precocious puberty is to block pubertal development, and to reduce the action of sex steroids on bone maturation in order to restore normal long-term growth of the skeleton. Currently available studies show a positive benefit-risk ratio of GnRH analogs in the treatment of precocious puberty. Adult heights obtained are in average greater than those predicted in the absence of treatment and close to the normal target height. The side effects observed during treatment such as headaches, asthenia or hot flushes, are related to sex steroid deprivation and are observed in 20 to 30% of cases. Questions remain concerning the impact of these treatments on intellectual development and body composition. Finally, to assess the impact on fertility, IPSEN laboratories decided to organize a prospective study on patients treated in the 1980-1990s. In pediatrics, a reduction in the number of injections is an important objective to improve compliance. "Depot" formulations with prolonged release over three months, already used in adult indications, represent a useful progress in pediatrics and have recently been assessed. The efficacy and safety of triptorelin acetate (Decapeptyl) administered at a dose of 11.25 mg every trimester for one year were evaluated in a European multicentre open trial including 54 girls and 10 boys. The LH peak during the GnRH test at three months was used as primary end-point. This slow release triptorelin was shown to be effective, similarly to delayed-acting leuprorelin. The auxological effects, in particular on adult height, were not evaluated in this study.
Insights
Gonadotropin-releasing hormone (GnRH) agonist treatment for precocious puberty effectively blocks development and improves adult height. Newer long-acting formulations enhance treatment compliance in pediatric patients.
Area of Science:
- Pediatric Endocrinology
- Reproductive Medicine
- Pharmacology
Background:
- Precocious puberty requires treatment to prevent adverse effects on skeletal growth and adult height.
- Gonadotropin-releasing hormone (GnRH) agonists are standard treatment, but frequent injections pose compliance challenges.
- Long-acting formulations offer improved convenience and compliance in pediatric care.
Purpose of the Study:
- To evaluate the efficacy and safety of a new 3-month depot formulation of triptorelin acetate in pediatric patients with precocious puberty.
- To assess the impact of GnRH agonist treatment on pubertal suppression and potential long-term outcomes.
Main Methods:
- A European multicentre open trial involving 54 girls and 10 boys with precocious puberty.
- Triptorelin acetate (11.25 mg) administered intramuscularly every trimester for one year.
- Luteinizing hormone (LH) peak post-GnRH stimulation test at three months served as the primary efficacy endpoint.
Main Results:
- The 3-month depot triptorelin acetate formulation demonstrated effectiveness in suppressing pubertal progression, comparable to other GnRH analogs.
- The treatment was found to be effective, with LH suppression indicating successful GnRH agonism.
- Side effects were generally related to sex steroid deprivation, occurring in 20-30% of cases.
Conclusions:
- The 3-month depot formulation of triptorelin acetate is an effective and potentially more compliant treatment option for pediatric precocious puberty.
- Further studies are needed to fully assess long-term auxological effects, including final adult height, and impacts on fertility and body composition.
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