RecruitingPhase 1NCT06366490

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

Phase 1 Study to Assess the Safety and Immunogenicity of Innocell Autologous Cellular Immunotherapy Administered in Patients With Recurrent Epithelial Ovarian Cancer


Sponsor

PhotonPharma, Inc.

Enrollment

8 participants

Start Date

Feb 12, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

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


Eligibility

Sex: FEMALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a new personalized immune cell therapy called Innocell — made from the patient's own immune cells — in women with recurrent ovarian, fallopian tube, or peritoneal cancer who have already received platinum-based chemotherapy. **You may be eligible if...** - You are a woman aged 18 or older - You have advanced epithelial ovarian, fallopian tube, or primary peritoneal cancer confirmed by biopsy or cytology - You have received at least 1 prior line of platinum-based chemotherapy - Your cancer has returned and you are a candidate for single-agent therapy **You may NOT be eligible if...** - You have carcinosarcoma - You have active or uncontrolled infection - You have received more treatments than the study allows - You are pregnant or breastfeeding Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BIOLOGICALInnocell Autologous Cellular Immunotherapy

Innocell Autologous Cellular Immunotherapy cells will be administered with CpG 1018 adjuvant ID every 2 weeks x 3 doses


Locations(1)

City of Hope

Duarte, California, United States

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NCT06366490


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