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NCT07596212 · ClinicalTrials.gov registry record · Phase 1

BRE-06: Study to Increase Tolerance to Aromatase Inhibitors for Patients With Early-Stage Hormone Receptor Positive Breast Cancer Who Developed Hypoactive Sexual Desire Disorder

A Phase 1 study, sponsored by University of Illinois at Chicago.

Not yet
Registry status
Phase 1
Development phase
100
Enrollment target

NCT07596212 is a Phase 1 study that has not yet begun recruiting, run by University of Illinois at Chicago. The registered enrollment target is 100 participants.

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The verdict

NCT07596212, a Phase 1 study, has not yet begun recruiting, sponsored by University of Illinois at Chicago.

NOT YET RECRUITING
Registry status
Phase 1
Development phase
100 participants
Enrollment target

Study Summary

This study is open to women who have early-stage breast cancer and are on aromatase inhibitor (AI) therapy, and who have hypoactive sexual desire disorder (HSDD). HSDD is a persistent lack of physical desire for sex and a lack of sexual activity, or even sexual thoughts or fantasies, that causes you distress. The researchers want to determine if sexual functioning, as measured by responses on a sexual functioning questionnaire, is improved by adding Bupropion Extended Release (XL) to the AI treatment regimen. Bupropion XL is an FDA-approved medication for the treatment of major depressive disorder, seasonal affective disorder, and nicotine dependence. It has been studied in HSDD in pre- and post-menopausal healthy women, and has been demonstrated to be effective, but it has not been thoroughly studied in women with early-stage breast cancer on AI therapy.

Interventions

  • DRUG Bupropion
  • DRUG GnRH agonist
  • DRUG Aromatase Inhibitors

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2026-07
Est. Completion 2031-07
Phase Phase 1

Sponsor

University of Illinois at Chicago

430 total trials

What the Registry Record Tells You About NCT07596212

The ClinicalTrials.gov registry entry for NCT07596212 describes a study currently listed as not yet recruiting, categorized as Phase 1. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Illinois at Chicago, which has 430 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 3 interventions - of which Bupropion is the first listed.

NCT07596212 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT07596212 about?

NCT07596212 is a clinical study titled "BRE-06: Study to Increase Tolerance to Aromatase Inhibitors for Patients With Early-Stage Hormone Receptor Positive Breast Cancer Who Developed Hypoactive Sexual Desire Disorder". This study is open to women who have early-stage breast cancer and are on aromatase inhibitor (AI) therapy, and who have hypoactive sexual desire disorder (HSDD). HSDD is a persistent lack of physical desire for sex and a lack of sexual activity, or even sexual thoughts or fantasies, that causes you...

What is the current status of trial NCT07596212?

This trial is currently not yet recruiting. It is a Phase 1 study. The enrollment target is 100 participants. The study started on 2026-07. Estimated completion is 2031-07.

What interventions are being tested in trial NCT07596212?

The interventions under investigation include: Bupropion (DRUG), GnRH agonist (DRUG), Aromatase Inhibitors (DRUG).

Who is sponsoring clinical trial NCT07596212?

This trial is sponsored by University of Illinois at Chicago, which has 430 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.