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This trial is complete. It is no longer accepting participants. Results may be available on ClinicalTrials.gov.

NCT02159716

NCT02159716
Completed Phase 1

Who may be able to join

Who might be able to join this trial:

  • You have been diagnosed with one of the following cancers, confirmed by a tissue sample (biopsy): pancreatic cancer that has spread to other parts of the body; ovarian cancer or a related abdominal cancer that has come back or not gone away; or a type of lung lining cancer called epithelial malignant pleural mesothelioma.
  • Your cancer has continued or come back after trying at least one standard chemotherapy treatment.
  • Your cancer can be measured on a scan using standard methods.
  • You are older than 18 years of age.
  • You are generally able to carry out daily activities with little to no limitation (confirm with trial site for exact fitness level required).
  • Doctors expect you to live for more than 3 months.
  • Your blood counts, kidney, liver, and heart are working well enough to meet specific levels set by the trial (confirm with trial site for exact values).
  • Your blood clotting is within an acceptable range, or you are on stable blood-thinning medication for a clot related to your cancer (confirm with trial site).
  • You are willing and able to understand and sign a written consent form.
  • If you are able to have children, you agree to use an approved form of contraception during the study and for 6 months after receiving the treatment cells.

Who may not be able to join:

  • You have a type of mesothelioma called sarcomatoid or biphasic, as these types do not respond to this treatment.
  • You have taken part in another clinical trial using an experimental drug within the last 28 days, or you plan to use another experimental drug during this trial.
  • You are expected to need standard chemotherapy within 2 weeks before the cell collection or treatment steps of this trial.
  • You have another active cancer that is spreading or invasive, beyond the three cancers listed above (some non-invasive skin or surface cancers may still be allowed — confirm with trial site).
  • You have HIV, hepatitis C (HCV), or hepatitis B (HBV).
  • You have an active autoimmune disease (such as lupus, rheumatoid arthritis, or multiple sclerosis) that has required immune-suppressing medication in the past 4 weeks, with the exception of thyroid hormone replacement.
  • You currently have an ongoing or active infection.
  • You are planned to receive high-dose steroid medication at the same time as this trial (a low, stable dose for a breathing condition may be acceptable — confirm with trial site).
  • You need extra oxygen to breathe.
  • You have previously received any treatment involving gene-modified cells.
  • You have previously received an experimental treatment involving a specific protein called SS1, or certain types of mouse-based antibody therapies (confirm with trial site).
  • You have a known allergy to mouse proteins.
  • You have a known allergy or bad reaction to any ingredients in the study treatment, including human serum albumin, DMSO, or Dextran 40.
  • You have a significant fluid build-up around your heart, moderate to severe heart failure, or another heart condition that could be made worse by this treatment or make it hard to monitor certain side effects.
  • You have a significant fluid build-up around your lungs or abdomen that cannot be drained using standard methods (having a drainage tube already in place before joining may be acceptable).
  • You are pregnant or breastfeeding, or your pregnancy test comes back positive before starting treatment.

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.

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.

Trial details

Status
Completed
Phase
Phase 1
Sponsor
University of Pennsylvania
Registry
clinicaltrials_gov
Start date
1 June 2014
Est. completion
1 November 2015

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Number of 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: 30 June 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

View original record on ClinicalTrials.gov