Phase 2 Ovarian Cancer Trial, Recruiting NCT06839144 Sponsor: Tel-Aviv Sourasky Medical Center Condition: Ovarian Cancer
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Phase 2 Ovarian Cancer Trial, Recruiting

NCT06839144
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:

  • People aged between 20 and 85 years old
  • People who are in generally good to moderate overall health, as assessed by standard medical scoring tools (ASA score 1–3 or ECOG score 0–2)
  • People who have imaging, physical examination, blood test results (CA125), and/or a tumour biopsy suggesting a high-grade ovarian cancer of a specific type (epithelial)
  • People who are scheduled for surgery to remove ovarian cancer, either as a first operation or as a later "interval" debulking surgery
  • People who have signed a consent form agreeing to take part
  • People who are physically and mentally able to follow the study procedures

Who may not be able to join:

  • People who are currently taking part in another interventional clinical trial
  • People who have a known allergy to any of the study medications, or to any anti-inflammatory drug (NSAID) or beta-blocker medication
  • People who regularly take any type of beta-blocker or COX-inhibiting medication (a type of anti-inflammatory), with the exception of aspirin — though aspirin must be stopped at least 7 days before surgery and not resumed until 3 weeks after surgery
  • People who currently have active asthma, or who needed hospital treatment or a change in asthma medication within the past year
  • People who currently have an active stomach ulcer or peptic disease
  • People who have had a stroke or mini-stroke (CVA or TIA) at any point in the past
  • People who have had another cancer within the last 5 years, or who currently have another cancer — exceptions may apply for certain fully treated skin or cervical conditions (confirm with trial site)
  • People with kidney failure, indicated by a creatinine blood test result above 1.5
  • People with significant liver problems, including cirrhosis or a bilirubin blood test level above 2
  • People with significant heart failure (classified as NYHA class 3 or higher)
  • People with a slow heart rate of 50 beats per minute or fewer, or with certain heart rhythm problems known as second- or third-degree AV block
  • People with right-sided heart failure caused by high blood pressure in the lungs (pulmonary hypertension)
  • People who regularly take a heart medication called Digoxin
  • People who have a condition called Prinzmetal's angina (a type of chest pain caused by coronary artery spasm)
  • People who have been diagnosed with significant enlargement of the heart (cardiomegaly)
  • People with a heart rhythm condition called sick sinus syndrome
  • People with disease affecting the blood vessels in their arms or legs (peripheral vascular disease)
  • People who currently have an unremoved tumour of the adrenal gland called a pheochromocytoma
  • People who are pregnant
  • People who are taking immune-suppressing medications, including steroid tablets at doses above the equivalent of 10 mg of prednisone per day, or any other immune-suppressing therapy taken within 7 days before the first study drug dose
  • People who have an immune deficiency disorder

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 14 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: Nadav Michaan, Prof., Tel Aviv Sourasky Medical Center (Ichilov Hospital)

Phone: 972-3-6407266

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
Registry
ClinicalTrials.gov
Start date
12 March 2025
Est. completion
31 August 2026

Where this trial is recruiting

🇮🇱 Israel

Primary endpoints

Transcriptional Activity in Excised Tumors; Transcriptional Activity in Blood Samples; Adverse Event Assessment; Patient Adherence to Drug Regimen; Recruitment Rate

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: 14 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