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Recruiting Phase 1 NCT06366490

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

Trial Parameters

Condition Ovarian Cancer
Sponsor PhotonPharma, Inc.
Study Type INTERVENTIONAL
Phase Phase 1
Enrollment 8
Sex FEMALE
Min Age 18 Years
Max Age N/A
Start Date 2026-02-12
Completion 2026-11
Interventions
Innocell Autologous Cellular Immunotherapy

Brief Summary

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

Eligibility Criteria

Inclusion Criteria: 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 clin

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