Phase 1 Ovarian Cancer Trial, Recruiting NCT07665515 Sponsor: Epitopea Ltd Condition: Ovarian Cancer
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Phase 1 Ovarian Cancer Trial, Recruiting

NCT07665515
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 able to understand and willing to sign the consent form and follow the study procedures
  • You are female and aged 18 or older at the time of signing consent
  • You have been diagnosed (confirmed by lab testing of tissue) with a specific type of ovarian, fallopian tube, or peritoneal cancer (high-grade serous or similar high-grade type)
  • Your cancer was classified as Stage III or IV when first diagnosed
  • You had surgery to remove as much of the cancer as possible, leaving no more than 1 cm of remaining tumour
  • You have completed a first course of platinum-based chemotherapy (at least 4 cycles of carboplatin and paclitaxel, or a similar treatment, given before and/or after surgery)
  • After chemotherapy, your cancer either showed a complete or partial response, or showed no signs of getting worse, based on scans assessed by your doctor
  • Your last dose of first-line chemotherapy was at least 4 weeks ago but no more than 12 weeks ago at the time of screening
  • There is no sign that your cancer has come back or grown between finishing chemotherapy and your screening visit
  • Your cancer has been tested and confirmed as BRCA wildtype (a specific genetic result) and HRP (homologous recombination proficient — confirm with trial site)
  • You have not had, and are not currently having or planning to have, bevacizumab or a PARP inhibitor as a maintenance treatment after first-line chemotherapy
  • Your general health and ability to carry out daily activities meets a specific standard (ECOG score of 0 or 1 — confirm with trial site)
  • Your blood counts and organ function (such as liver and kidneys) are within acceptable ranges
  • If you are able to become pregnant, you have had a negative pregnancy test
  • Your immune system tissue type (HLA type) matches the study's specific requirements (confirm with trial site)

Who may not be able to join:

  • You have a type of ovarian tumour that is non-epithelial or considered low risk/borderline
  • You have uncontrolled fluid build-up around your abdomen or lungs that needed draining within the last 4 weeks before screening
  • You have another active cancer, or have had another cancer in the past 3 years (with some exceptions for very low-risk cancers — confirm with trial site)
  • You have an active autoimmune disease (where your immune system attacks your own body) that requires ongoing medication to suppress your immune system
  • You have another serious illness that, in the doctor's opinion, could put you at risk or affect how the study is carried out
  • You have had a severe allergic reaction (anaphylaxis) to a type of treatment called mRNA-LNP therapy (such as certain vaccines — confirm with trial site)
  • You have previously received a cancer vaccine, a checkpoint inhibitor, or a cell-based cancer therapy
  • You have received any vaccine in the 30 days before your first dose in the study
  • You have taken part in another clinical trial involving an experimental medicine in the past 90 days (or longer, depending on the drug — confirm with trial site)

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 6 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

Principal Investigator: Susana Banerjee, MBBS MA FRCP PhD, Royal Marsden NHS Foundation Trust

Phone: +4530660105

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
Epitopea Ltd
Registry
ClinicalTrials.gov
Start date
1 July 2026
Est. completion
1 March 2029

Where this trial is recruiting

🇬🇧 United Kingdom

Primary endpoints

To evaluate the safety and tolerability of CryptiVax-1001; To evaluate the safety and tolerability of CryptiVax-1001; To evaluate the safety and tolerability of CryptiVax-1001; To evaluate the safety and tolerability of CryptiVax-1001

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: 6 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