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Completed Phase 3 Interventional Results available

Safety and Quality of Life Study of Aflibercept in Patients With Metastatic Colorectal Cancer Previously Treated With an Oxaliplatin-Based Regimen

ClinicalTrials.gov ID: NCT01571284

Public ClinicalTrials.gov record NCT01571284. 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 19, 2026, 5:11 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 Multicenter, Single Arm, Open Label Clinical Trial to Evaluate the Safety and Health-Related Quality of Life of Aflibercept in Patients With Metastatic Colorectal Cancer (mCRC) Previously Treated With an Oxaliplatin-Containing Regimen

Brief summary

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

Primary Objective: To provide metastatic colorectal cancer participants with access to aflibercept and to document the overall safety in these participants Secondary Objective: To document the Health-Related Quality of Life of aflibercept in this participants population

Study identification

NCT ID
NCT01571284
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Sanofi
Industry
Enrollment
781 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
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
May 30, 2012 (Actual)
Primary completion
Jan 31, 2017 (Actual)
Completion
Jan 31, 2017 (Actual)
Last update posted
Apr 17, 2018

2012 – 2017

United States locations

U.S. sites
12
U.S. states
9
U.S. cities
12
Facility City State ZIP Site status
Investigational Site Number 840-002 Muscle Shoals Alabama 35661 —
Investigational Site Number 840-008 Corona California 92879 —
Investigational Site Number 840-007 Fountain Valley California 92708 —
Investigational Site Number 840-004 Riverside California 92501 —
Investigational Site Number 840-006 Indianapolis Indiana 46254 —
Investigational Site Number 840-011 Metairie Louisiana 70006 —
Investigational Site Number 840-001 Rockville Maryland 20850 —
Investigational Site Number 840-010 Howell Township New Jersey 07731 —
Investigational Site Number 840-012 Albuquerque New Mexico 87106 —
Investigational Site Number 840-009 Farmington New Mexico 87401 —
Investigational Site Number 840-003 Lake Success New York 11042 —
Investigational Site Number 840-005 Middletown Ohio 45042 —

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 167 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01571284, 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 Apr 17, 2018 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01571284 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →