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Terminated Phase 2 Interventional Results available

Tivozanib in Combination With Paclitaxel in Patients With Locally Recurrent or Metastatic Triple Negative Breast Cancer

ClinicalTrials.gov ID: NCT01745367

Public ClinicalTrials.gov record NCT01745367. 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 Oct 24, 2026, 6:03 PM 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 Phase 2 Randomized, Double-Blind, Placebo-Controlled, Study Comparing Tivozanib Hydrochloride in Combination With Paclitaxel v Placebo in Combination With Paclitaxel in Locally Recurrent and/or Metastatic Triple Negative Breast Cancer

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a phase 2 multicenter, double-blind, randomized, placebo-controlled, two-arm study for subjects with locally recurrent or metastatic triple negative breast cancer.

Study identification

NCT ID
NCT01745367
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
AVEO Pharmaceuticals, Inc.
Industry
Enrollment
30 participants

Conditions and interventions

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
Nov 2012 (Type not available)
Primary completion
Jun 2014 (Actual)
Completion
Jun 2014 (Actual)
Last update posted
Oct 27, 2020

2012 – 2014

United States locations

U.S. sites
20
U.S. states
15
U.S. cities
20
Facility City State ZIP Site status
Not listed Birmingham Alabama 35005 —
Not listed Jacksonville Florida 32034 —
Not listed Miami Florida 33018 —
Not listed Atlanta Georgia 30301 —
Not listed Chicago Illinois 60007 —
Not listed Oak Lawn Illinois 60456 —
Not listed Fort Wayne Indiana 46774 —
Not listed Indianapolis Indiana 46077 —
Not listed Baltimore Maryland 21201 —
Not listed Boston Massachusetts 01841 —
Not listed St Louis Missouri 63101 —
Not listed New York New York 10001 —
Not listed The Bronx New York 10453 —
Not listed Chapel Hill North Carolina 27514 —
Not listed Fargo North Dakota 58102 —
Not listed Charleston South Carolina 02129 —
Not listed Sioux Falls South Dakota 57101 —
Not listed Memphis Tennessee 37501 —
Not listed Dallas Texas 75001 —
Not listed Galveston Texas 77550 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 34 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01745367, 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 Oct 27, 2020 · Synced Oct 24, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01745367 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →