Phase 2 Ovarian Cancer Trial, Recruiting NCT06815497 Sponsor: Tyler J Curiel Condition: Ovarian Cancer
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Phase 2 Ovarian Cancer Trial, Recruiting

NCT06815497
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You are 18 years of age or older
  • You are able to carry out daily activities with little to no limitation, or with some limitations but still able to care for yourself (your doctor will assess this)
  • You are willing and able to give your agreement to participate in the study
  • You have been diagnosed with a specific type of ovarian cancer called high-grade serous ovarian carcinoma, confirmed by a tissue sample test
  • Your ovarian cancer has continued to grow or came back within 6 months of your last platinum-based chemotherapy treatment (meaning it is resistant or not responding to that treatment)
  • You are able to receive standard chemotherapy treatments approved for ovarian cancer
  • Your doctors expect you to live for at least 2 months
  • Your blood counts are at acceptable levels, meaning your white blood cells, platelets, and hemoglobin (red blood cell measure) meet minimum levels without a recent blood transfusion
  • Your liver is working well enough, based on blood test results
  • Your kidneys are working well enough, based on blood test results
  • Your blood clotting levels are within an acceptable range (unless you are already on blood-thinning medication)
  • If you could become pregnant, you must agree to use highly effective birth control during the study and for at least 3 months after your last chemotherapy dose
  • If you could become pregnant, you must have a negative pregnancy blood test within 72 hours before starting the study medication
  • You have no medical reasons that would prevent you from taking a medication called telmisartan, and you have not taken a type of blood pressure medication called an ACE inhibitor in the 6 weeks before starting telmisartan on this trial
  • Your systolic blood pressure (the top number in a blood pressure reading) is at or above 110 mmHg when you join and throughout the study

Who may not be able to join:

  • You are unable or unwilling to give your agreement to participate
  • You have a significant liver disease that is currently active, such as viral hepatitis, alcohol-related liver disease, or liver scarring (cirrhosis); however, patients with certain managed hepatitis B or C conditions may still be considered (confirm with trial site)
  • You are experiencing a severe, dangerous spike in blood pressure (hypertensive urgency or emergency)
  • You are currently incarcerated or homeless
  • You are pregnant or breastfeeding
  • You are under 18 years of age
  • You are currently taking a medication called lithium in any form
  • You received certain medications called rituximab or amifostine within the last 30 days before starting the study medication
  • You have a serious active infection that requires treatment
  • You have significant heart or blood vessel problems, such as a heart attack or stroke in the past 6 months, unstable chest pain, certain levels of heart failure, or a serious irregular heartbeat requiring medication
  • You have any other condition, treatment, or health issue that, in your doctor's opinion, could interfere with the trial results or would not be in your best interest
  • You are currently taking a medication called ramipril
  • Your standard chemotherapy treatment includes a medication called bevacizumab
  • You are HIV-positive and your HIV viral load is not undetectable by standard testing methods

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 5 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Ivy Wilkinson-Ryan, MD, Dartmouth Health

Phone: 603-650-5000

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Tyler J Curiel
Registry
ClinicalTrials.gov
Start date
21 January 2026
Est. completion
14 April 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Progression free survival

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 5 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov