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NCT04032080 · ClinicalTrials.gov registry record · Phase 2

LY3023414 and Prexasertib in Metastatic Triple-negative Breast Cancer

A Phase 2 study, sponsored by Baylor Research Institute.

Completed
Registry status
Phase 2
Development phase
10
Enrollment target

NCT04032080: Completed Phase 2 study, sponsored by Baylor Research Institute.

NCT04032080 is a Phase 2 study that has completed, run by Baylor Research Institute. The registered enrollment target is 10 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04032080, a Phase 2 study, has completed, sponsored by Baylor Research Institute.

COMPLETED
Registry status
Phase 2
Development phase
10 participants
Enrollment target

Study Summary

This study evaluates efficacy of LY3023414 and prexasertib in patients with metastatic triple negative breast cancer.

Primary Outcome

To assess the objective response rate associated with LY3023414 and prexasertib in metastatic TNBC patients. Objective response is measured as prolonged clinical benefit; clinical benefit is defined as progression free survival on study therapy for at least 6 months.

Interventions

  • COMBINATION_PRODUCT Drug 1: LY3023414; Drug 2: Prexasertib

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2019-09-05
Est. Completion 2022-11-26
Phase Phase 2
Baylor Research Institute

180 total trials

What the finished NCT04032080 record still lists

NCT04032080 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (92% lower).

The record links to 0 conditions, and to 1 intervention - of which Drug 1: LY3023414; Drug 2: Prexasertib is the first listed.

NCT04032080 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04032080 about?

NCT04032080 is a clinical study titled "LY3023414 and Prexasertib in Metastatic Triple-negative Breast Cancer". This study evaluates efficacy of LY3023414 and prexasertib in patients with metastatic triple negative breast cancer.

What is the current status of trial NCT04032080?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 10 participants. The study started on 2019-09-05. Estimated completion is 2022-11-26.

What interventions are being tested in trial NCT04032080?

The interventions under investigation include: Drug 1: LY3023414; Drug 2: Prexasertib (COMBINATION_PRODUCT).

Who is sponsoring clinical trial NCT04032080?

This trial is sponsored by Baylor Research Institute, which has 180 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04032080's enrollment target sits among peer trials

10 1968th of 2000 higher than 12 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT04032080, the US trial registry maintained by the National Library of Medicine. NCT04032080 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.