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Spots Global Cancer Trial Database for Study of Safety & Biological Activity of IP IMNN-001 (Also Known as GEN-1) With Neoadjuvant Chemo in Ovarian Cancer

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Trial Identification

Brief Title: Study of Safety & Biological Activity of IP IMNN-001 (Also Known as GEN-1) With Neoadjuvant Chemo in Ovarian Cancer

Official Title: A Phase I Study of the Safety and Biological Activity of Intraperitoneal IMNN-001 (IL-12 Plasmid Formulated With PEG-PEI-Cholesterol Lipopolymer) Administered In Combination With Standard Neoadjuvant Chemotherapy in Patients Newly Diagnosed With Epithelial Ovarian, Fallopian Tube or Primary Peritoneal Cancer

Study ID: NCT02480374

Interventions

IMNN-001

Study Description

Brief Summary: This dose escalation study will determine a maximum tolerated dose and/or optimal biological dose of GEN-1 for carboplatin/paclitaxel combination in newly diagnosed ovarian cancer.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

University of Alabama Birmingham Cancer Center, Birmingham, Alabama, United States

Washington Univ. in St. Louis/Barnes Jewish Hospital, Saint Louis, Missouri, United States

Stephenson Cancer Center, Oklahoma City, Oklahoma, United States

Medical College of Wisconsin/Froedtert Hospital, Milwaukee, Wisconsin, United States

Contact Details

Name: Premal Thaker, M.D.

Affiliation: Washington University School of Medicine

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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