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RECRUITING
NCT05328258
PHASE3

Use of GnRHa During Chemotherapy for Fertility Protection

Sponsor: Kenny Rodriguez-Wallberg

View on ClinicalTrials.gov

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.

Official title: A Phase 3 Randomised Double-Blinded Placebo-Controlled Study of Use of GnRHa During Chemotherapy for Fertility Protection of Young Women and Teenagers With Cancer

Key Details

Gender

FEMALE

Age Range

14 Years - 42 Years

Study Type

INTERVENTIONAL

Enrollment

500

Start Date

2023-03-31

Completion Date

2032-01-31

Last Updated

2023-10-27

Healthy Volunteers

No

Interventions

DRUG

Triptorelin Embonate

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.

DRUG

Sodium Chloride solution 0.9%

One injection compensating for 3 months' effect OR one injection compensating for 1 month' effect to maintain the study blind.

Locations (17)

Center for Pediatric Cancer, Queen Silvia Hospital for Children and Youth

Gothenburg, Sweden

Center for Pediatric Oncology, Akademiska Hospital

Gothenburg, Sweden

Department of Oncology, Sahlgrenska University Hospital

Gothenburg, Sweden

Department of Hematology, Skåne University Hospital

Lund, Sweden

Department of Oncology, Skåne University Hospital

Lund, Sweden

Department of Pediatric Oncology, Skåne University Hospital

Lund, Sweden

Department of Oncology, Örebro University Hospital

Örebro, Sweden

Karolinska Univeristy Hospital, Breast Centre

Stockholm, Sweden

Department of Hematology and coagulation, Sahlgrenska University Hospital

Stockholm, Sweden

Department of Hematology, Capio ST. Göran Hospital

Stockholm, Sweden

Department of Internal Medicine, Södersjukhuset

Stockholm, Sweden

Department of Oncology, Capio ST. Göran Hospital

Stockholm, Sweden

Department of Oncology, Södersjukhuset

Stockholm, Sweden

Division of Hematology, Department of Medicine Huddinge, Karolinska Institutet

Stockholm, Sweden

Karolinska University Hospital, Hematology

Stockholm, Sweden

Karolinska University Hospital, High Specialised Pediatric Medicine

Stockholm, Sweden

Department of Oncology, Norrlands University Hospital

Umeå, Sweden