RecruitingOvarian CancerRecurrent Epithelial Ovarian Cancer Which Includes Epithelial Ovarian, Fallopian Tube and/or Primary Peritoneal Cancer

Safety and Immunogenicity of Innocell Autologous Cellular Immunotherapy for Recurrent Epithelial Ovarian Cancer

Eligible age

18+ yrs

Accepts

Women

Locations

1 state

Healthy volunteers

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Safety and Immunogenicity of Innocell Autologous Cellular Immunotherapy Administered in Patients with Recurrent Epithelial Ovarian Cancer

Sponsor: PhotonPharma, Inc.

✓ 1. Age ≥ 18 years and female;
✓ 2. Has histologically or cytologically confirmed diagnosis of advanced epithelial ovarian cancer (except carcinosarcoma), primary peritoneal, or fallopian tube cancer that has received at least 1 line of platinum-based systemic therapy and for whom single-agent therapy is appropriate as the next line of treatment;
✓ 3. Been treated with available standard-of-care therapy likely to convey clinical benefit (i.e., PARP inhibitors for women with germline BRCA mutation and in homologous recombination repair deficiency based on prior molecular testing or bevacizumab as appropriate);
✓ 4. Documented relapse or progression on or after the most recent line of therapy;
✓ 5. Patients must have at least 2 sites of measurable or detectable disease. The team will target to collect 1.0 gram of tumor tissue that can be removed and be available for manufacturing;
✓ 6. Eastern Collaborative Oncology Group (ECOG) performance status (PS) 0-2;
✓ 7. Recovery from clinically relevant toxicities to Grade 2 or less (except alopecia, peripheral neuropathy, and ototoxicity);
✓ 8. Adequate hematological, hepatic, and renal function obtained ≤ 28 days prior to planned initiation of vaccine series

✕ 1. Positive clinical history of HIV, HCV, HBV, HTLV-1/2;
✕ 2. Diagnosis of immunodeficiency, either primary or acquired;
✕ 3. Active or prior history of autoimmune disease;
✕ Note: The following conditions are permitted (i.e., not exclusionary) if the condition does not require immunosuppressive treatment:
✕ Type 1 diabetes (if stable, well controlled, and not brittle); Vitiligo; Hypo- or hyperthyroid disease; or Autoimmune alopecia.
✕ 4. Treatment with systemic steroids or any other form of immunosuppressive therapy within 14 days prior to planned initiation of the Innocell vaccine; Note: Inhaled or topical steroids, including mouthwash, and adrenal replacement doses are permitted in the absence of active autoimmune disease.
✕ 5. Has any acute infection that requires specific therapy. Acute therapy must be completed at least 7 days prior to initiation of Innocell series;
✕ 6. Has received any live or attenuated vaccines against infectious diseases within 28 days of the planned vaccine initiation. Inactive vaccines, including SARS-CoV-2 vaccines authorized for use for active immunization to prevent COVID-19 are allowed and must be given in accordance with the prevailing immunization guidelines; or

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Source: ClinicalTrials.gov · NCT06366490 · last updated 2026-03-27