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Search / Trial NCT06650423

Adherence to Aromatase Inhibitors ± Abemaciclib Treatment in Patients With Early-stage HER2-negative Breast Cancer

Launched by ERIKA MATOS · Oct 18, 2024

Trial Information

Current as of June 26, 2025

Not yet recruiting

Keywords

Breast Cancer Medication Adherence Cdk4/6 Hr+ Her2 Aromatase Inhibitor Quality Of Life Medication Belief

ClinConnect Summary

This clinical trial is studying how well patients with early-stage, hormone receptor-positive, HER2-negative breast cancer stick to their medication, particularly those taking a combination of aromatase inhibitors and a drug called abemaciclib. About 70% of breast cancer patients fall into this category, and even with treatments, some still face a risk of their cancer coming back. Researchers want to find out if patients taking both types of medication have a harder time following their treatment plan compared to those taking aromatase inhibitors alone. They believe factors like a patient’s quality of life, mental well-being, and previous treatment experiences may influence how consistently they take their medication.

To participate in this trial, women must be diagnosed with early-stage HR+/HER2- breast cancer and currently receiving treatment with an aromatase inhibitor for no more than 18 months. They should be able to communicate in Slovenian and provide consent to join the study. The trial is not yet recruiting, but if you qualify and choose to participate, you’ll help researchers understand how to improve treatment adherence, which is crucial for the effectiveness of breast cancer therapy.

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • Female,
  • Early HR+/HER-2- BC,
  • Patient is receiving adjuvant therapy with an aromatase inhibitor (letrozole, anastrozole or exemestane), with or without a CDK4/6 inhibitor abemaciclib, for no more than 18 months,
  • Treatment of BC is being conducted at OIL,
  • Patient has mandatory health insurance through Health Insurance Institute of Slovenia,
  • Patient understands Slovenian language, and
  • Patient agrees to participate in the study and provides written informed consent.
  • Exclusion Criteria:
  • Metastatic HR+/HER-2- BC
  • Previous treatment for BC with an aromatase inhibitor, with or without a CDK4/6 inhibitor, due to BC.

About Erika Matos

Erika Matos is a dedicated clinical trial sponsor committed to advancing medical research through innovative and ethically responsible studies. With a focus on enhancing patient outcomes, Ms. Matos leverages her extensive expertise in clinical operations and regulatory compliance to design and implement trials that meet rigorous scientific and ethical standards. Her collaborative approach fosters strong relationships with healthcare professionals, regulatory bodies, and research institutions, ensuring that each trial is conducted with integrity and transparency. Through her leadership, Erika Matos aims to contribute significantly to the development of novel therapies and improve the lives of patients worldwide.

Locations

Patients applied

0 patients applied

Trial Officials

Erika Matos, PhD

Principal Investigator

Institute of Oncology Ljubljana, Slovenia

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported