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Clinical Trial Summary

Collection of data in real life conditions on satefy, effectiveness and quality of life of trastuzumab deruxtecan in patients with metastatic or unresectable HER2-positive breast cancer.


Clinical Trial Description

The present observational study aims to collect data on long-term safety of trastuzumab deruxtecan, with a primary endpoint on trastuzumab deruxtecan related adverse drug reactions (ADRs) of interest. Data on patient profile, treatment history (before, during and after trastuzumab deruxtecan administration), effectiveness and health-related quality of life will also be collected in a real-life setting, to confirm and complement data from clinical trials. Patients will be recruited whether they have started trastuzumab deruxtecan treatment or will start it at the time of inclusion, whether they were prescribed compassionate trastuzumab deruxtecan or marketed Enhertu®, in order to rapidly collect a large set of data. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05149014
Study type Observational [Patient Registry]
Source Daiichi Sankyo France
Contact Ines FETTAR
Phone + 33 1 55 62 15 36
Email ines.fettar@daiichi-sankyo.fr
Status Recruiting
Phase
Start date December 14, 2021
Completion date July 2024

See also
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