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NCT03414047 · ClinicalTrials.gov registry record · Phase 2

A Study of Prexasertib (LY2606368) in Platinum-Resistant or Refractory Recurrent Ovarian Cancer

A Phase 2 study of Ovarian Cancer, sponsored by Eli Lilly and Company.

Completed
Registry status
Phase 2
Development phase
172
Enrollment target
20
Study locations

NCT03414047 is a Phase 2 study of Ovarian Cancer that has completed, run by Eli Lilly and Company. The registered enrollment target is 172 participants, below the 728-participant average among 322 other Ovarian Cancer trials with a reported enrollment target (76% lower). The trial reports 20 study locations across 15 states.

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The verdict

NCT03414047, a Phase 2 study of Ovarian Cancer, has completed, sponsored by Eli Lilly and Company.

COMPLETED
Registry status
Phase 2
Development phase
172 participants
Enrollment target
20
Study locations

Study Summary

The purpose of this study is to evaluate the efficacy and safety of prexasertib in women with platinum-resistant or refractory recurrent ovarian cancer.

Conditions Studied

Interventions

  • DRUG Prexasertib

Study Locations (20)

Tennessee

  • University of Tennessee Medical Center - Knoxville
  • Sarah Cannon Research Institute SCRI - Nashville
  • Tennessee Oncology PLLC - Nashville

New South Wales

  • Concord Repatriation General Hospital - Concord
  • Prince of Wales Hospital - Randwick
  • Westmead Hospital - Wentworthville

Queensland

  • Royal Brisbane and Womens Hospital - Herston
  • Mater Adult Hospital Brisbane - South Brisbane

Arizona

  • Arizona Oncology Associates, P.C. - Tucson

California

  • Kaiser Permanente Medical Center - Vallejo

Florida

  • University of Southern Florida School of Medicine - Gainesville

Massachusetts

  • Dana Farber Cancer Institute - Boston

Missouri

  • Research Medical Center - Kansas City

Trial Details

FieldValue
Enrollment Target 172 participants
Start Date 2018-04-10
Est. Completion 2020-10-03
Phase Phase 2

Sponsor

Eli Lilly and Company

1,341 total trials

What the Registry Record Tells You About NCT03414047

The ClinicalTrials.gov registry entry for NCT03414047 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 172 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 728-participant average among 322 other Ovarian Cancer trials with a reported enrollment target (76% lower). The listed sponsor is Eli Lilly and Company, which has 1,341 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Ovarian Cancer appearing as the primary indexed condition, and to 1 intervention - of which Prexasertib is the first listed.

NCT03414047 reports 20 study locations spanning 15 distinct geographic areas - top geographies include Tennessee, New South Wales, Queensland.

Frequently Asked Questions

What is clinical trial NCT03414047 about?

NCT03414047 is a clinical study titled "A Study of Prexasertib (LY2606368) in Platinum-Resistant or Refractory Recurrent Ovarian Cancer". The purpose of this study is to evaluate the efficacy and safety of prexasertib in women with platinum-resistant or refractory recurrent ovarian cancer.

What is the current status of trial NCT03414047?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 172 participants. The study started on 2018-04-10. Estimated completion is 2020-10-03.

What conditions does trial NCT03414047 study?

This clinical trial studies the following conditions: Ovarian Cancer.

What interventions are being tested in trial NCT03414047?

The interventions under investigation include: Prexasertib (DRUG).

Who is sponsoring clinical trial NCT03414047?

This trial is sponsored by Eli Lilly and Company, which has 1,341 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03414047 being conducted?

This trial has 20 study locations across Arizona, California, Florida, Massachusetts, Missouri. 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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.