Phase 3 Ovarian Cancer Trial, Recruiting NCT05281471 Sponsor: Genelux Corporation Condition: Ovarian Cancer
Back to Ovarian Cancer

Phase 3 Ovarian Cancer Trial, Recruiting

NCT05281471
Recruiting Phase 3

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 have been diagnosed with ovarian, fallopian tube, or primary peritoneal cancer that cannot be surgically removed, confirmed by a tissue biopsy from a previous treatment.
  • Your cancer is one of these specific types: high-grade serous, endometrioid, or clear-cell ovarian cancer (certain mixed tumors may also qualify — confirm with trial site).
  • You are generally able to carry out daily activities with little or no limitation (your doctor rates your physical fitness as 0 or 1 on a standard scale).
  • Your doctor expects you to live for at least 6 more months.
  • You have already received at least 3 rounds (lines) of cancer treatment, including your first-line treatment.
  • Your cancer has either stopped responding to platinum-based chemotherapy during treatment, or came back within 6 months of finishing it.
  • You have previously been treated with bevacizumab (or a similar drug).
  • You have no medical reason that would prevent you from receiving carboplatin, cisplatin, or bevacizumab.
  • Your cancer has gotten worse after your most recent treatment, confirmed by a scan.
  • You have at least one measurable area of cancer visible on an abdominal or pelvic scan.
  • Scans or a physical exam show that cancer is likely present inside the abdominal cavity (on the lining of the abdomen).
  • Your kidneys, liver, blood counts, blood clotting, and immune system are all functioning at an adequate level.

Who may not be able to join:

  • Your cancer is of a specific type not covered by this trial, such as mucinous, low-grade serous, squamous cell, small cell, or non-epithelial types (e.g., germ cell or sex-cord tumors).
  • You have had a bowel blockage in the last 3 months.
  • You currently have an active infection, such as a urinary tract infection, pneumonia, or other serious infection.
  • You are currently experiencing active bleeding in your digestive system.
  • Cancer has spread to your brain or spinal cord.
  • You have an inflammatory bowel disease (such as Crohn's disease or ulcerative colitis).
  • You have a known history of HIV infection.
  • You have had an active hepatitis B or hepatitis C infection within the last 4 weeks.
  • You have had a blood clot in a vein or artery in the past 3 months.
  • Certain physical conditions of your abdomen would make it unsafe to place the catheter used in this trial (confirm with trial site).
  • You have serious heart problems rated as Class III or IV by your doctor.
  • You have had a stroke or mini-stroke (TIA) in the past 6 months.
  • Your blood oxygen level is below 90%.
  • You have previously received a virus-based gene therapy or treatment using a virus designed to destroy cancer cells.
  • You are currently taking antiviral medication.
  • You have had another type of cancer that was active in the past 3 years (some early-stage or easily cured skin, bladder, or cervical cancers may still be acceptable — confirm with trial site).
  • You have received chemotherapy, radiation, or other cancer treatments within the past 4 weeks.
  • You have had surgery within the past 4 weeks, or have not fully healed from a recent surgery.
  • You are currently taking immune-suppressing drugs or steroids above a certain dose (confirm with trial site).
  • You have rapidly worsening fluid build-up in your abdomen or around your lungs that requires draining more than once every 14 days.
  • You have a known allergy to the antibiotic gentamicin.

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 28 July 2026
Phase 3: approximately ~65% 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.

GP referral letter

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

Trial details

Status
Recruiting
Phase
Phase 3
Sponsor
Genelux Corporation
Registry
ClinicalTrials.gov
Start date
31 August 2022
Est. completion
1 December 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Progression-free survival (PFS) by RECIST 1.1 in the Intention-to-Treat (ITT) population (all randomized participants regardless of whether they received any dose of treatment)

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: 28 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