Phase 1 Ovarian Cancer Trial, Recruiting NCT06366490 Sponsor: PhotonPharma, Inc. Condition: Ovarian Cancer
Back to Ovarian Cancer

Phase 1 Ovarian Cancer Trial, Recruiting

NCT06366490
Recruiting Phase 1

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 a woman aged 18 or older
  • You have been diagnosed with advanced ovarian cancer, primary peritoneal cancer, or fallopian tube cancer (confirmed by a lab test), excluding a type called carcinosarcoma, and have received at least one round of platinum-based chemotherapy
  • You have already received standard treatments that were likely to help you, such as PARP inhibitors (if you have a BRCA gene mutation or a related gene repair problem) or bevacizumab, if those were appropriate for you
  • Your cancer has come back or gotten worse after your most recent treatment
  • You have at least 2 areas of cancer that can be measured or detected, and enough tumor tissue can be safely removed for the trial's manufacturing process (about 1 gram)
  • You are generally well enough to carry out daily activities, based on a standard health scale rated 0–2 (confirm with trial site)
  • Any side effects from previous treatments have mostly resolved, except for hair loss, nerve-related issues, or hearing problems
  • Your blood, liver, and kidney test results are within acceptable ranges, tested within 28 days before the trial starts
  • If you could become pregnant, you have a negative pregnancy test and agree to use reliable contraception throughout the trial
  • You are willing and able to sign a consent form agreeing to take part

Who may not be able to join:

  • You have a history of HIV, Hepatitis C (HCV), Hepatitis B (HBV), or HTLV-1/2 infections
  • You have been diagnosed with any condition that weakens your immune system, whether inherited or acquired
  • You have an active or past history of an autoimmune disease — though some conditions may be allowed if they do not require immune-suppressing treatment, such as stable Type 1 diabetes, vitiligo, thyroid conditions, or autoimmune hair loss (confirm with trial site)
  • You have taken steroid tablets or other immune-suppressing medicines within 14 days before the trial vaccine is due to start (inhaled or topical steroids are generally allowed)
  • You currently have an active infection requiring treatment that has not fully cleared at least 7 days before the trial starts
  • You have received a live or weakened (attenuated) vaccine for an infectious disease within 28 days before the trial vaccine is due to start (inactive vaccines, including most COVID-19 vaccines, are generally allowed)
  • You have taken part in another clinical trial and received an experimental treatment within 4 weeks before the trial starts
  • You have received an approved cancer treatment within 3 weeks before the trial starts
  • You have had a previous different cancer, unless it was fully treated and has not returned within the last 5 years (some treated skin cancers may be exceptions — confirm with trial site)
  • You have any other health condition, circumstance, or history that the trial doctor believes could affect the trial results or make participation not in your best interest
  • You are unable to follow the trial's procedures or attend follow-up appointments

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 20 July 2026
Phase 1: approximately ~10% 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

Phone: 303-981-1120

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 1
Sponsor
PhotonPharma, Inc.
Registry
ClinicalTrials.gov
Start date
12 February 2026
Est. completion
1 November 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Success rate of autologous manufacturing; Safety assessed by treatment emergent adverse events

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: 20 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