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Clinical Trial Summary

The MINERVA Trial aims to evaluate safety, efficacy and quality of life (QoL) for the combination of Abemaciclib with an Aromatase Inhibitor or Fulvestrant in pre- and postmenopausal patients with metastatic hormone receptor positive HER2 negative breast cancer in the first line setting. Side effect monitoring and patient reported outcomes will be captured using the web- and app-based CANKADO digital health application. Via this user-friendly tool the patients can document their therapy side effects (e.g. diarrhea) and outcomes on a day-to-day basis. The capturing of side effects using the digital health application will be done additionally to the regular AE documentation. Furthermore, translational research objectives of this trial include the investigation of biomarkers (ct-DNA, germline DNA) to evaluate whether they can give insights into the reasons for response, intrinsic or acquired resistance to the combined endocrine


Clinical Trial Description

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Study Design


Related Conditions & MeSH terms


NCT number NCT05362760
Study type Interventional
Source University of Ulm
Contact Natalie Uhl
Phone +49 731 500 58652
Email natalie.uhl@uniklinik-ulm.de
Status Recruiting
Phase Phase 4
Start date April 27, 2022
Completion date April 2029

See also
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Completed NCT05261269 - A Dose-escalation Study of the Safety and Pharmacology of DAN-222 in Subjects With Metastatic Breast Cancer Phase 1
Completed NCT02605915 - Safety and Pharmacokinetics of Atezolizumab Combination Treatments in Participants With HER2-Positive and HER2-Negative Breast Cancer Phase 1
Recruiting NCT04720729 - Chemotherapy Monitoring by ctDNA in HER2- Metastatic Breast Cancer Phase 2