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Clinical Trial Summary

The primary objective of the trial is to determine the effect of a 24-week concomitant coaching on patient reported outcomes of patients receiving standard treatment for mRCC with sunitinib or a combination of pembrolizumab + axitinib or avelumab + axitinib in first line therapy.


Clinical Trial Description

The goal of our study is to define the benefit of proactive coaching in mRCC, when compared to a reactive approach, which is considered the standard of care. Patients in the Coaching Arm A will be trained continuously at personal interactions of coach and patient (Face-to Face meetings as well as telephone contacts). The patient is educated on nature and severity of treatment emergent Adverse events (TEAE) of sunitinib or a combination of pembrolizumab + axitinib or avelumab + axitinib in first line therapy. Quality of Life (QoL) is assessed during sunitinib treatment in both arms (Arm A Coaching and Arm B non Coaching). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03013946
Study type Interventional
Source AIO-Studien-gGmbH
Contact Mischo Kursar, Dr.
Phone +49 30 8145 344
Email Mischo.Kursar@aio-studien-ggmbh.de
Status Recruiting
Phase Phase 3
Start date January 18, 2017
Completion date July 31, 2024

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