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NCT03332576 · ClinicalTrials.gov registry record · Phase 1

Phase 1b Study of a Cancer Vaccine to Treat Patients With Advanced Stage Ovarian, Fallopian or Peritoneal Cancer

A Phase 1 study of Fallopian Tube Cancer and Epithelial Ovarian Cancer, sponsored by ImmunoVaccine Technologies, Inc. (IMV Inc.).

Completed
Registry status
Phase 1
Development phase
37
Enrollment target
3
Study locations

NCT03332576 is a Phase 1 study of Fallopian Tube Cancer and Epithelial Ovarian Cancer that has completed, run by ImmunoVaccine Technologies, Inc. (IMV Inc.). The registered enrollment target is 37 participants, below the 255-participant average among 85 other Fallopian Tube Cancer trials with a reported enrollment target (85% lower). The trial reports 3 study locations across 2 states.

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The verdict

NCT03332576, a Phase 1 study of Fallopian Tube Cancer and Epithelial Ovarian Cancer, has completed, sponsored by ImmunoVaccine Technologies, Inc. (IMV Inc.).

COMPLETED
Registry status
Phase 1
Development phase
37 participants
Enrollment target
3
Study locations

Study Summary

As a follow-on study to NCT01416038, this study is designed to identify the optimal dosage of immunotherapeutic survivin vaccine DPX-Survivac and low dose oral cyclophosphamide. The combination treatment is being evaluated in a non-randomized, multi-cohort study as post-chemotherapy treatment for patients with late-stage ovarian, fallopian tube, or peritoneal cancer.

Interventions

  • DRUG Cyclophosphamide
  • BIOLOGICAL DPX-Survivac
  • BIOLOGICAL DPX-Survivac(Aqueous)

Study Locations (3)

New York

  • Winthrop University Hospital - Mineola
  • Lenox Hill Hospital - New York

Ontario

  • Princess Margaret Cancer Centre - Toronto

Trial Details

FieldValue
Enrollment Target 37 participants
Start Date 2013-08-23
Est. Completion 2019-09-09
Phase Phase 1

What the Registry Record Tells You About NCT03332576

The ClinicalTrials.gov registry entry for NCT03332576 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 37 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 255-participant average among 85 other Fallopian Tube Cancer trials with a reported enrollment target (85% lower). The listed sponsor is ImmunoVaccine Technologies, Inc. (IMV Inc.), which has 6 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 3 interventions - of which Cyclophosphamide is the first listed.

NCT03332576 reports 3 study locations spanning 2 distinct geographic areas - top geographies include New York, Ontario.

Frequently Asked Questions

What is clinical trial NCT03332576 about?

NCT03332576 is a clinical study titled "Phase 1b Study of a Cancer Vaccine to Treat Patients With Advanced Stage Ovarian, Fallopian or Peritoneal Cancer". As a follow-on study to NCT01416038, this study is designed to identify the optimal dosage of immunotherapeutic survivin vaccine DPX-Survivac and low dose oral cyclophosphamide. The combination treatment is being evaluated in a non-randomized, multi-cohort study as post-chemotherapy treatment for pa...

What is the current status of trial NCT03332576?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 37 participants. The study started on 2013-08-23. Estimated completion is 2019-09-09.

What conditions does trial NCT03332576 study?

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

What interventions are being tested in trial NCT03332576?

The interventions under investigation include: Cyclophosphamide (DRUG), DPX-Survivac (BIOLOGICAL), DPX-Survivac(Aqueous) (BIOLOGICAL).

Who is sponsoring clinical trial NCT03332576?

This trial is sponsored by ImmunoVaccine Technologies, Inc. (IMV Inc.), which has 6 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03332576 being conducted?

This trial has 3 study locations across New York, Ontario. 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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