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Terminated Phase 2 Interventional Results available

Pilot Study to Evaluate Safety & Biological Effects of Orally Administered Reparixin in Early Breast Cancer

ClinicalTrials.gov ID: NCT01861054

Public ClinicalTrials.gov record NCT01861054. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 24, 2026, 4:12 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Single Arm, Preoperative, Pilot Study to Evaluate the Safety and Biological Effects of Orally Administered Reparixin in Early Breast Cancer Patients Who Are Candidates for Surgery

Study identification

NCT ID
NCT01861054
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Dompé Farmaceutici S.p.A
Industry
Enrollment
20 participants

Conditions and interventions

Conditions

Interventions

  • Reparixin Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 31, 2013
Primary completion
Feb 28, 2015
Completion
Feb 29, 2016
Last update posted
May 13, 2021

2013 – 2016

United States locations

U.S. sites
9
U.S. states
7
U.S. cities
9
Facility City State ZIP Site status
Indiana University Simon Cancer Center Indianapolis Indiana 46202-5289
University of Kansas Cancer Center, 4350 Shawnee Mission Pkwy, Suite 1500, Mailstop 6004 Fairway Kansas 66205
The Cancer Institute of New Jersey New Brunswick New Jersey 08903
Weill Cornell Medical College New York New York 10065
Montefiore Medical Center, MMC Medical Park at Eastchester The Bronx New York 10461
Fox Chase Cancer Center Philadelphia Pennsylvania 19111
Magee-Womens Hospital Pittsburgh Pennsylvania 15213
Sara Cannon Research Institute Nashville Tennessee 37203
The Methodist Hospital Research Institute Houston Texas 77030

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01861054, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 13, 2021 · Synced Jul 24, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01861054 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →