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
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.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
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