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Clinical Trial Summary

The goal of this clinical trial is to learn about the tolerability of telmisartan in patients with prostate cancer.


Clinical Trial Description

The primary objective of this study is to test the tolerability of oral telmisartan given as a single agent or combined with specific standard of care agents in selected participants with PC. Patients will be defined as tolerating telmisartan if they maintain systolic blood pressure >110 mm Hg and are without greater than grade 2 toxicities as defined in the Common Terminology Criteria for Adverse Events v5.1 for at least 60 days total telmisartan treatment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06168487
Study type Interventional
Source Dartmouth-Hitchcock Medical Center
Contact Kayla Fay
Phone 603-650-5000
Email kayla.a.fay@hitchcock.org
Status Not yet recruiting
Phase Early Phase 1
Start date June 1, 2024
Completion date April 1, 2027

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