RecruitingPhase 1NCT06168487

Telmisartan in Prostate Cancer

Phase I Non-Randomized, Unblinded, Single-Center Trial of Oral Telmisartan Alone or Combined With Selected Standard of Care Therapies for Prostate Cancer


Sponsor

Tyler J Curiel

Enrollment

36 participants

Start Date

Apr 22, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

The goal of this clinical trial is to learn about the tolerability of telmisartan in patients with prostate cancer, but evidence for treatment efficacy will also be gathered.


Eligibility

Sex: MALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing whether adding telmisartan — a common blood pressure drug — alongside standard prostate cancer treatment can improve outcomes. Lab studies suggest telmisartan may help cancer drugs work better. **You may be eligible if...** - You are 18 or older with prostate cancer that is being treated with specific standard regimens (including docetaxel, cabazitaxel, olaparib, rucaparib, or talazoparib plus enzalutamide) - Your cancer is stable or progressing on PSA but without requiring an immediate change in treatment - You have adequate liver and kidney function - Your standing blood pressure is at least 110 mmHg systolic - You have testosterone at castrate levels (if not on active surveillance) **You may NOT be eligible if...** - You have a contraindication to telmisartan (including recent ACE inhibitor use in the last 6 weeks) - Your blood pressure is too low to safely take telmisartan throughout the study Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGTelmisartan

Patients will be given telmisartan alone or with standard of care chemotherapy.

OTHERStandard of Care Regimen

Standard of Care Regimen


Locations(1)

Dartmouth Health

Lebanon, New Hampshire, United States

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NCT06168487


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