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Aromatase Inhibitor
Tamoxifen + Letrozole for Fertility Preservation in Breast Cancer (TALES Trial)
Phase 3
Recruiting
Led By Mitchell Rosen, MD
Research Sponsored by University of California, San Francisco
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 2 weeks
Awards & highlights
No Placebo-Only Group
Pivotal Trial
Summary
This trial is testing two medication combinations to help women with breast cancer preserve their fertility. It focuses on women with a specific type of breast cancer and aims to find out which combination helps produce more mature eggs. The medications work by managing hormone levels and stimulating the ovaries. Tamoxifen and letrozole have been used to safely manage hormone levels in breast cancer patients undergoing fertility preservation.
Who is the study for?
This trial is for adults over 18 who have been newly diagnosed with breast cancer and wish to preserve fertility before starting chemotherapy. They must want to undergo ovarian stimulation and egg retrieval.
What is being tested?
The study is testing the effectiveness of two drugs, Tamoxifen and Letrozole, in increasing the number of eggs retrieved for preservation from patients with estrogen-sensitive tumors before they start cancer treatment.
What are the potential side effects?
Possible side effects include hot flashes, mood swings, joint pain, and fatigue. There may also be a risk of blood clots or changes in menstrual flow.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 2 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 2 weeks
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Mature Oocyte Yield
Secondary study objectives
Compare change in androgen levels during the ovarian stimulation cycle
Compare change in estrogen in follicular fluid
Compare change in estrogen levels during the ovarian stimulation cycle
+5 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Pivotal Trial
The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Trial Design
3Treatment groups
Experimental Treatment
Active Control
Group I: ER Positive - TamoxifenExperimental Treatment1 Intervention
Group II: ER Positive - LetrozoleExperimental Treatment1 Intervention
Group III: ER NegativeActive Control1 Intervention
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Tamoxifen
2005
Completed Phase 4
~30110
Letrozole
2002
Completed Phase 4
~3590
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Letrozole plus Gonadotropin and Tamoxifen plus Gonadotropin are common treatments for infertility. Letrozole, an aromatase inhibitor, reduces estrogen production, leading to increased follicle-stimulating hormone (FSH) levels, which stimulates the ovaries to produce multiple follicles.
Gonadotropins are hormones that directly stimulate the ovaries to produce multiple follicles. Tamoxifen, a selective estrogen receptor modulator (SERM), blocks estrogen receptors, also resulting in increased FSH levels and ovarian stimulation.
These treatments are designed to enhance ovarian stimulation and improve oocyte yield, thereby increasing the chances of successful fertilization and pregnancy for infertility patients.
Fertility preservation for women with breast cancer: a multicentre randomized controlled trial on various ovarian stimulation protocols.Concomitant tamoxifen or letrozole for optimal oocyte yield during fertility preservation for breast cancer: the TAmoxifen or Letrozole in Estrogen Sensitive tumors (TALES) randomized clinical trial.Does daily co administration of gonadotropins and letrozole during the ovarian stimulation improve IVF outcome for poor and sub optimal responders?
Fertility preservation for women with breast cancer: a multicentre randomized controlled trial on various ovarian stimulation protocols.Concomitant tamoxifen or letrozole for optimal oocyte yield during fertility preservation for breast cancer: the TAmoxifen or Letrozole in Estrogen Sensitive tumors (TALES) randomized clinical trial.Does daily co administration of gonadotropins and letrozole during the ovarian stimulation improve IVF outcome for poor and sub optimal responders?
Find a Location
Who is running the clinical trial?
University of California, San FranciscoLead Sponsor
2,585 Previous Clinical Trials
15,084,045 Total Patients Enrolled
18 Trials studying Infertility
8,725 Patients Enrolled for Infertility
Mitchell Rosen, MDPrincipal InvestigatorUniversity of California, San Francisco
4 Previous Clinical Trials
502 Total Patients Enrolled
3 Trials studying Infertility
500 Patients Enrolled for Infertility
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:Research Study Groups:
This trial has the following groups:- Group 1: ER Positive - Tamoxifen
- Group 2: ER Negative
- Group 3: ER Positive - Letrozole
Awards:
This trial has 2 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- Pivotal Trial - The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Infertility Patient Testimony for trial: Trial Name: NCT03011684 — Phase 3
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