RecruitingPhase 3NCT06915025
Phase 3 Trial Evaluating the Safety & Efficacy of IMNN-001 Administered in Combination w/ Standard NACT & Adjuvant Chemotherapy in Newly Diagnosed Patients w/ Advanced EOC, Fallopian Tube or Primary Peritoneal Cancer
Studying Primary peritoneal carcinoma
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Imunon
- Principal Investigator
- Premal H Thaker, M.D.Washington University School of Medicine
- Intervention
- IMNN-001 (IL-12 Plasmid Formulated with PEG-PEI-Cholesterol Lipopolymer)(drug)
- Enrollment
- 500 enrolled
- Eligibility
- 18 years · FEMALE
- Timeline
- 2025 – 2032
Study locations (7)
- Advent Health, Orlando, Florida, United States
- Washington University School of Medicine in St. Louis, St Louis, Missouri, United States
- Providence Cancer Institute, Portland, Oregon, United States
- Sanford Health, Sioux Falls, South Dakota, United States
- Erlanger Health, Chattanooga, Tennessee, United States
- Providence Sacred Heart Medical Center & Children's Hospital, Spokane, Washington, United States
- Froedtert and The Medical College of Wisconsin, Milwaukee, Wisconsin, United States
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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