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NCT02480374 · ClinicalTrials.gov registry record · Phase 1

Study of Safety & Biological Activity of IP IMNN-001 (also Known As GEN-1) with Neoadjuvant Chemo in Ovarian Cancer

A Phase 1 study of Fallopian Tube Cancer and Epithelial Ovarian Cancer, sponsored by Imunon.

Completed
Registry status
Phase 1
Development phase
18
Enrollment target
4
Study locations

NCT02480374 is a Phase 1 study of Fallopian Tube Cancer and Epithelial Ovarian Cancer that has completed, run by Imunon. The registered enrollment target is 18 participants, below the 256-participant average among 85 other Fallopian Tube Cancer trials with a reported enrollment target (93% lower). The trial reports 4 study locations across 4 states.

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The verdict

NCT02480374, a Phase 1 study of Fallopian Tube Cancer and Epithelial Ovarian Cancer, has completed, sponsored by Imunon.

COMPLETED
Registry status
Phase 1
Development phase
18 participants
Enrollment target
4
Study locations

Study 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.

Interventions

  • BIOLOGICAL IMNN-001

Study Locations (4)

Alabama

  • University of Alabama Birmingham Cancer Center - Birmingham

Missouri

  • Washington Univ. in St. Louis/Barnes Jewish Hospital - St Louis

Oklahoma

  • Stephenson Cancer Center - Oklahoma City

Wisconsin

  • Medical College of Wisconsin/Froedtert Hospital - Milwaukee

Trial Details

FieldValue
Enrollment Target 18 participants
Start Date 2015-09
Est. Completion 2017-05
Phase Phase 1

Sponsor

Imunon

11 total trials

What the Registry Record Tells You About NCT02480374

The ClinicalTrials.gov registry entry for NCT02480374 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 18 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 256-participant average among 85 other Fallopian Tube Cancer trials with a reported enrollment target (93% lower). The listed sponsor is Imunon, which has 11 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Fallopian Tube Cancer appearing as the primary indexed condition, and to 1 intervention - of which IMNN-001 is the first listed.

NCT02480374 reports 4 study locations spanning 4 distinct geographic areas - top geographies include Alabama, Missouri, Oklahoma.

Frequently Asked Questions

What is clinical trial NCT02480374 about?

NCT02480374 is a clinical study titled "Study of Safety & Biological Activity of IP IMNN-001 (also Known As GEN-1) with Neoadjuvant Chemo in Ovarian Cancer". 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.

What is the current status of trial NCT02480374?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 18 participants. The study started on 2015-09. Estimated completion is 2017-05.

What conditions does trial NCT02480374 study?

This clinical trial studies the following conditions: Fallopian Tube Cancer, Epithelial Ovarian Cancer, Primary Peritoneal Cancer.

What interventions are being tested in trial NCT02480374?

The interventions under investigation include: IMNN-001 (BIOLOGICAL).

Who is sponsoring clinical trial NCT02480374?

This trial is sponsored by Imunon, which has 11 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02480374 being conducted?

This trial has 4 study locations across Alabama, Missouri, Oklahoma, Wisconsin. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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