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Clinical Trials in Sweden / NCT05328258
Recruiting Phase 3

Use of GnRHa During Chemotherapy for Fertility Protection

NCT05328258 · tracked via the Priya Life Science Sweden tracker
Sponsor
Kenny Rodriguez-Wallberg
Phase
Phase 3
Started
2023-03-31
Last updated
2023-10-27

Condition(s) studied

Breast Cancer FemaleAcute LeukemiaLymphomaOsteosarcomaSoft Tissue SarcomaEwing Sarcoma

Investigational drug(s) / intervention(s)

Triptorelin Embonate →Sodium Chloride solution 0.9%

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.

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.

Study 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.

Eligibility

Sex
FEMALE
Min age
14 Years
Max age
42 Years
Healthy volunteers
No
Inclusion Criteria: * Signed informed consent * Breast cancer or acute leukemias, lymphomas (Hodgkin and non-Hodgkin) or sarcomas (osteo, soft tissue and Ewing) confirmed by histology and assigned for diseace-specific chemotheraphy * Confirmed menarche * ECOG performance status 0-1 * Adequate bone marrow, renal, hepatic and cardiac functions and absence of other uncontrolled medical or psychiatric disorders Exclusion Criteria: * Demonstrated premature ovarian failure at time of randomization according to clinical or biochemical data * Previous or planned bilateral oophorectomy * Pregnancy or breastfeeding at time of start of chemotherapy * Other malignancy diagnosed within the last five years * Uncontrolled hypertension, heart, liver, kidney related or other uncontrolled medical or psychiatric disorders including previous or current diagnosis of anorexia * Known osteoporosis * Known low platelet count with increased bleeding risk or refractory thrombocytopenia in subjects with acute leukemias * Known or suspected allergy against triptorelin * Direct radiation of the gonads previous or planned (TBI allowed) * Mental inability, reluctance or language difficulties that result in difficulty understanding the meaning of study participation

Primary outcome measure(s)

Trial sites (17)

FacilityCityRegionStatus
Center for Pediatric Cancer, Queen Silvia Hospital for Children and Youth Gothenburg Sweden Not Yet Recruiting
Center for Pediatric Oncology, Akademiska Hospital Gothenburg Sweden Not Yet Recruiting
Department of Oncology, Sahlgrenska University Hospital Gothenburg Sweden Not Yet Recruiting
Department of Hematology, Skåne University Hospital Lund Sweden Not Yet Recruiting
Department of Oncology, Skåne University Hospital Lund Sweden Not Yet Recruiting
Department of Pediatric Oncology, Skåne University Hospital Lund Sweden Not Yet Recruiting
Department of Oncology, Örebro University Hospital Örebro Sweden Active Not Recruiting
Karolinska Univeristy Hospital, Breast Centre Stockholm Sweden Recruiting
Department of Hematology and coagulation, Sahlgrenska University Hospital Stockholm Sweden Not Yet Recruiting
Department of Hematology, Capio ST. Göran Hospital Stockholm Sweden Not Yet Recruiting
Department of Internal Medicine, Södersjukhuset Stockholm Sweden Not Yet Recruiting
Department of Oncology, Capio ST. Göran Hospital Stockholm Sweden Not Yet Recruiting
Department of Oncology, Södersjukhuset Stockholm Sweden Not Yet Recruiting
Division of Hematology, Department of Medicine Huddinge, Karolinska Institutet Stockholm Sweden Recruiting
Karolinska University Hospital, Hematology Stockholm Sweden Recruiting
Karolinska University Hospital, High Specialised Pediatric Medicine Stockholm Sweden Recruiting
Department of Oncology, Norrlands University Hospital Umeå Sweden Not Yet Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05328258 on ClinicalTrials.gov ↗ ← All trials in Sweden