RecruitingPhase 2NCT06815497

Telmisartan in Combination With Cytotoxic Regimens in Platinum-Resistant Ovarian Cancer

Phase II Non-Randomized, Unblinded, Single-Center Trial of Telmisartan in Combination With Cytotoxic Regimens in Platinum-Resistant Ovarian Cancer Versus Historical Best Supportive Care


Sponsor

Tyler J Curiel

Enrollment

33 participants

Start Date

Jan 21, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The primary study objective is to assess progression-free survival in patients with ovarian cancer receiving telmisartan plus selected standard of care chemotherapy regimens versus historical controls.


Eligibility

Sex: FEMALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing whether adding a blood pressure drug called telmisartan to standard chemotherapy helps treat platinum-resistant ovarian cancer — cancer that has stopped responding to platinum-based chemotherapy drugs. Telmisartan is thought to affect cancer cell survival, and researchers want to see if it can make chemotherapy more effective. **You may be eligible if...** - You are 18 or older - You have high-grade serous ovarian cancer that is resistant or refractory to platinum chemotherapy (meaning it came back or grew within 6 months of your last platinum treatment) - You are in reasonable health (ECOG performance status 0–2) - You are scheduled to receive standard chemotherapy for ovarian cancer - You have a life expectancy of at least 2 months **You may NOT be eligible if...** - You have severe organ dysfunction or poor blood counts - You are pregnant or breastfeeding - You have uncontrolled infections 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

Telmisartan will be introduced as a 40 mg tablet to be taken orally once daily. In participants not experiencing telmisartan dose limiting toxicity, the dose will be escalated to a maximum of 80 mg


Locations(2)

Dartmouth Hitchcock

Lebanon, New Hampshire, United States

Dartmouth-Hitchcock Manchester

Manchester, New Hampshire, United States

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NCT06815497


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