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Clinical Trial Summary

The purpose of this study is to quantify and publish participants' relative preferences for outcomes of chemotherapy and novel oral hormonal agents when added to androgen deprivation therapy (ADT) for participants with locally-advanced and metastatic hormone-sensitive prostate cancer (mHSPC). This study will also quantify the importance of administration factors related to convenience relative to treatment outcomes.


Clinical Trial Description

The study will develop and administer a discrete-choice experiment (DCE) to quantify tradeoff preferences of participants with mHSPC and locally-advanced prostate cancer in various countries. Data/surveys are being collected in: United States, Canada, UK, France, Spain, Japan, China and South Korea. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05381311
Study type Observational
Source Astellas Pharma Inc
Contact
Status Completed
Phase
Start date September 3, 2021
Completion date December 11, 2022

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