Related Experiment Video
Updated: Mar 5, 2026

Establishment of Rat Models Mimicking Gender-affirming Hormone Therapies
Published on: January 10, 2025
Meta-Analysis of Paediatric Patients with Central Precocious Puberty Treated with Intramuscular Triptorelin 11.25 mg
Adélaïde Durand1, Maithé Tauber1, Bharat Patel2
1Unité de Pédiatrie, Endocrinologie, Obésité, Maladies Osseuses, Génétique et Gynécologie Médicale, Hôpital des Enfants, CHU de Toulouse, Toulouse, France.
Insights
Triptorelin 11.25 mg effectively suppresses luteinizing hormone (LH) and other hormones in children with central precocious puberty (CPP). This 3-month formulation demonstrates efficacy in managing CPP progression.
Area of Science:
- Pediatric Endocrinology
- Reproductive Medicine
- Pharmacology
Background:
- Central precocious puberty (CPP) involves early onset of puberty due to premature activation of the hypothalamic-pituitary-gonadal axis.
- Effective management of CPP is crucial to prevent adverse outcomes such as short stature and psychosocial issues.
- Triptorelin, a gonadotropin-releasing hormone (GnRH) agonist, is a standard treatment for CPP.
Purpose of the Study:
- To evaluate the efficacy of the triptorelin 11.25 mg 3-month prolonged-release formulation in treating central precocious puberty (CPP).
- To assess the suppression of key hormonal markers indicative of pubertal progression.
Main Methods:
- A meta-analysis was conducted, including all available clinical studies of triptorelin 11.25 mg.
- The primary outcome measured was the proportion of children achieving suppressed luteinizing hormone (LH) response (peak LH ≤3 IU/L) 3 months post-injection.
- Secondary outcomes included hormonal suppression at 6 months and suppression of follicle-stimulating hormone (FSH), estradiol, and testosterone at 3 months.
Main Results:
- The study included 153 children (13 boys, 140 girls).
- A significant proportion of children achieved suppressed LH response: 87.6% at 3 months and 92.8% at 6 months.
- At 3 months, suppressed FSH, estradiol, and testosterone levels were observed in 86.7%, 97.1%, and 72.7% of children, respectively.
Conclusions:
- Triptorelin 11.25 mg administered every 3 months is an efficacious treatment for central precocious puberty.
- The formulation effectively suppresses LH peak and other gonadal hormones.
- This treatment aids in slowing the progression of CPP in pediatric patients.
Background/Aims:
A meta-analysis was undertaken to assess the effect of triptorelin 11.25 mg 3-month prolonged-release formulation in central precocious puberty (CPP).
Methods:
All available clinical studies with triptorelin 11.25 mg were included. The primary outcome was the proportion of children with suppressed luteinising hormone (LH) response (peak LH ≤3 IU/L) to the gonadotrophin-releasing hormone (GnRH) test 3 months after triptorelin 11.25 mg injection. Secondary outcomes included: the proportion with suppressed peak LH response at 6 months and the proportion with suppressed peak follicle-stimulating hormone (FSH) response (≤3 IU/L), suppressed oestradiol (≤20 pmol/L) in girls or suppressed testosterone (≤30 ng/dL) in boys at 3 months.
Results:
153 children (13 boys, 140 girls) were included. The proportion with a suppressed peak LH response to the GnRH test was 87.6% (95% CI: 81.3-92.4, p < 0.0001, for a proportion >70%) and 92.8% (95% CI: 87.5-96.4, p < 0.0001, for a proportion >70%) at 3 and 6 months, respectively. FSH peak, oestradiol, and testosterone were suppressed in 86.7% (95% CI: 79.1-92.4), 97.1% (95% CI: 91.6-99.4), and 72.7% (95% CI: 39.0-94.0) of children at 3 months, respectively.
Conclusion:
Triptorelin 11.25 mg 3-month formulation is efficacious in suppressing LH peak and other gonadal hormones and in slowing the progression of CPP in children. .
Related Concept Videos
Pharmacokinetics in Pediatric Patients: Drug Metabolism
Pharmacokinetics in Pediatric Patients: Drug Distribution
Pharmacokinetics in Pediatric Patients: Drug Excretion
Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption
Drug Accumulation During Multiple Dosing: Repetitive IV Injections
Dosage Regimens: Partial Pharmacokinetic Parameters

