ClinicalTrials.gov record
Active, not recruiting Phase 1Phase 2 Interventional

Study of IMNN-001 (Also Known as GEN-1) With NACT for Treatment of Ovarian Cancer (OVATION 2)

ClinicalTrials.gov ID: NCT03393884

Public ClinicalTrials.gov record NCT03393884. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 6, 2026, 8:11 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase I/II Study Evaluating the Dosing, Safety, Efficacy, and Biological Activity of Intraperitoneal IMNN-001 (IL-12 Plasmid Formulated With PEG-PEI-Cholesterol Lipopolymer) Administered in Combination With Neoadjuvant Chemotherapy (NACT) in Patients Newly Diagnosed With Advanced Epithelial Ovarian, Fallopian Tube or Primary Peritoneal Cancer

Study identification

NCT ID
NCT03393884
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Imunon
Industry
Enrollment
130 participants

Conditions and interventions

Interventions

  • Carboplatin Drug
  • IMNN-001 Biological
  • Paclitaxel Drug

Drug · Biological

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 4, 2018
Primary completion
Jul 24, 2024
Completion
May 29, 2026
Last update posted
May 3, 2026

2018 – 2026

United States locations

U.S. sites
20
U.S. states
13
U.S. cities
20
Facility City State ZIP Site status
University of Alabama Birmingham Birmingham Alabama 35233
Mitchell Cancer Institute (University of South Alabama) Mobile Alabama 36604
Gynecologic Oncology Associates (Hoag Hospital) Newport Beach California 92663
Innovative Clinical Research Whittier California 90603
Advent Health Orlando Florida 32803
Women's Care Florida St. Petersburg Florida 33701
Massachusetts General Hospital Boston Massachusetts 02114
Washington University School of Medicine in St. Louis St Louis Missouri 63110
MD Anderson at Cooper Camden New Jersey 08105
Hackensack University Medical Center Hackensack New Jersey 07601
Monter Cancer Center Lake Success New York 11042
NYU Langone, Long Island Mineola New York 11501
NYU Langone New York New York 10016
Stephenson Cancer Center - Oklahoma University Oklahoma City Oklahoma 73104
Providence Cancer Institute Portland Oregon 97213
Sanford Health Sioux Falls South Dakota 57104
Chattanooga Women's Health Chattanooga Tennessee 37403
The West Clinic Germantown Tennessee 38138
Providence Health Care Spokane Washington 99204
Medical College of Wisconsin Milwaukee Wisconsin 53226

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03393884, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 3, 2026 · Synced May 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03393884 live on ClinicalTrials.gov.

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