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Triptorelin

Decapeptyl, Trelstar, Gonapeptyl, Pamorelin

Quick Stats
Studies 178
Trials 100
Recruiting PHASE3 INTERVENTIONAL NCT05328258

Use of GnRHa During Chemotherapy for Fertility Protection

View on ClinicalTrials.gov Updated Dec 15, 2025

Brief Summary

Many cytotoxic drugs may harm the fertility of young women treated for cancer. The aim of the study is to investigate if the Gonadotropin-Releasing Hormone agonist (GnRHa) during cancer treatment can preserve the fertility of young female cancer subjects. Approximately 300 women with newly diagnosed breast cancer and up to 200 women with newly diagnosed lymphoma, acute leukemias or sarcomas will be recruited before start of cancer treatment. The patients will be randomised in between treatment with triptorelin (experimental) or placebo (control) intramuscularly a 1:1 ratio during chemotherapy. The injections may be given once monthly or once three months depending on type of chemotherapy given. Randomisation and study drug is blinded, neither investigator, research nurse nor patient will know if it is active drug or placebo. The only person who knows is the nurse preparing the injection. Patients will be followed up to 5 years after end of treatment with physical examinations, vital signs, biochemical markers, bone mineral density exams, ultrasound for antral follicle counts and ovarian doppler flow, concomitant medications, adverse events and quality of life questionnaires.

Interventions

Name: Triptorelin Embonate
Type: DRUG
Description: 11.25 mg will be given for subjects having at least 3 months gonadotoxic treatment, one injection of 11.25 mg will compensate for 3 months' effect of the study drug. 3.75 mg will be given for subjects during one-month of gonadotoxic treatment, one injection of 3.75 mg will compensate for 1 month' effect of the study drug.
Name: Sodium Chloride solution 0.9%
Type: DRUG
Description: One injection compensating for 3 months' effect OR one injection compensating for 1 month' effect to maintain the study blind.

Primary Outcomes

Measure: Anti-Müllerian Hormone (AMH) levels in women with breast cancer
TimeFrame: 12 months after end of gonadotoxic chemotherapy and study drug treatment
Description: To estimate the changes in ovarian reserve following chemotherapy for treatment of cancer with or without GnRHa by determination of the AMH relative to AMH levels at EoT in women with breast cancer.

Trial Information

NCT ID

NCT05328258

Status

Recruiting

Study Type

INTERVENTIONAL

Phases

PHASE3

Sponsor

Kenny Rodriguez-Wallberg

Last Updated

December 15, 2025