Actively Recruiting
Telmisartan in Prostate Cancer
Led by Tyler J Curiel · Updated on 2025-08-21
36
Participants Needed
1
Research Sites
153 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Telmisartan in Prostate Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Male participants aged 18 years or older
- Able and willing to provide informed consent or have a surrogate provide consent
- Stable prostate cancer patients not requiring immediate change in standard treatment
- Receiving or likely to receive specific standard care agents including cabazitaxel, docetaxel (alone or plus abiraterone), olaparib, rucaparib, or talazoparib plus enzalutamide
- ECOG performance status of 0 to 2
- Adequate liver and kidney function
- Standing systolic blood pressure of 110 mm Hg or higher
- Castrate level testosterone if not on active surveillance
- No contraindications to telmisartan, including no ACE inhibitor use within 6 weeks before starting telmisartan
- Ability to take or have taken own blood pressure per study protocol
- Hemoglobin above 10 gm/dl
- Blood prostate specific antigen above 1 ng/ml at study entry
- Able to tolerate planned blood draws
You will not qualify if you...
- Current or recent (within 30 days) use of angiotensin receptor blockers
- Hypertensive urgency or emergency
- Incarceration or homelessness
- Receiving prostate cancer treatments outside the approved agents or planned changes during the study, except local radiation
- Use of lithium therapy
- Recent rituximab or amifostine treatment within 30 days before telmisartan
- Use of ramapril
- Use of digoxin without consent to monthly blood level testing
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Dartmouth Health
Lebanon, New Hampshire, United States, 03756
Actively Recruiting
Research Team
K
Kayla Fay
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
2
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