Monthly vs. quarterly shots: can a simple switch boost ovarian suppression in young breast cancer?
NCT ID NCT07610733
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This Phase 2 trial will enroll 100 young women (ages 18-45) with hormone receptor-positive breast cancer who are already on a 3-month GnRH injection for ovarian suppression. Half will switch to a monthly injection, while the other half stays on the 3-month schedule. The study aims to see if the switch leads to better control of estrogen levels at 3 months, which is important for managing the disease.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- GnRH agonists (goserelin or leuprolide) plus endocrine therapy (aromatase inhibitor/tamoxifen ± CDK4/6 inhibitor)
- What this could lead to
- If successful, this could show that switching to a monthly GnRH injection provides better ovarian suppression, potentially improving treatment outcomes for young breast cancer patients.
- What could go wrong
- This is a small Phase 2 study (100 participants) and has not yet started recruiting. The primary endpoint is a hormone level, not a direct measure of cancer recurrence or survival, so benefits may not translate to better long-term outcomes.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jun 2026
An estimate. Start dates often move.
- Expected to finish
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Jun 2030
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 45 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: Step 1:iOFS detection phase 1. Female, aged ≥18 and ≤45 years; 2. Histologically confirmed hormone receptor-positive (HR+) (estrogen receptor \[ER\] and/or progesterone receptor \[PR\] ≥1%) and human epidermal growth factor receptor 2-negative (HER2-) early invasive breast cancer (stage I-III according to the American Joint Committee on Cancer \[AJCC\], version 8); 3. Completed curative surgery, with prior (neo)adjuvant chemotherapy and radiotherapy completed if applicable; 4. Currently receiving adjuvant therapy with a 3-month GnRH agonist (GnRHa) plus aromatase inhibitor (AI) or tamoxifen (TAM), with or without CDK4/6 inhibitors (excluding abemaciclib due to its potential interference with estradiol monitoring), for ≥1 dose, and presenting with estradiol (E2) ≥30 pg/mL within 28 days prior to enrollment (measured by CLIA). 5. Eastern Cooperative Oncology Group (ECOG) performance status score of 0-1; adequate bone marrow, hepatic, renal, and cardiac function. 6. Voluntarily sign a written informed consent form before the trial screening. Step 2:Randomized treatment phase 1. iOFS confirmed using the SEMS assay (E2 ≥30 pg/mL); 2. Ongoing adjuvant therapy with a 3-month GnRHa plus AI or TAM, with or without CDK4/6 inhibitors. 3. No evidence of disease progression. Exclusion Criteria: Step 1:iOFS detection phase 1. Bilateral breast cancer, inflammatory breast cancer, or distant metastasis; 2. Use of GnRHa for ovarian function preservation; 3. History of ovarian resection or ablation; planned pregnancy or breastfeeding; 4. Concomitant use of hormonal agents other than estrogen, progesterone, selective estrogen receptor modulators (SERM), or selective estrogen receptor degraders (SERD); 5. Severe uncontrolled comorbidities; 6. Other malignancies within the past 5 years (except for curatively treated carcinoma in situ of the cervix or basal cell carcinoma); 7. Failure to comply with follow-up or psychiatric disorders. Step 2:Randomized treatment phase a)Prior conversion from a 3-month GnRHa to a 1-month GnRHa.
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Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The study's own enquiry address
This study publishes an address for enquiries. See it below .
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
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Contacts and locations
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Genom att skicka in godkänner du våra Användarvillkor
Study contacts
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Contact
Email: •••••@•••••
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