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Terminated Phase 1Phase 2 Interventional Results available

A Study of Aflibercept Administered in Combination With Pemetrexed and Cisplatin in Participants With Advanced Carcinoma

ClinicalTrials.gov ID: NCT00794417

Public ClinicalTrials.gov record NCT00794417. 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 Nov 5, 2026, 2:42 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1/2 Study of Aflibercept Administered in Combination With Pemetrexed and Cisplatin in Patients With Advanced Carcinoma

Brief summary

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

The purpose of the study was to determine whether the combination of aflibercept, pemetrexed and cisplatin is safe and effective in treating non-small cell lung cancer (NSCLC).

Study identification

NCT ID
NCT00794417
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Regeneron Pharmaceuticals
Industry
Enrollment
60 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
Nov 30, 2008 (Actual)
Primary completion
Jun 30, 2011 (Actual)
Completion
Jun 30, 2011 (Actual)
Last update posted
Dec 10, 2020

2008 – 2011

United States locations

U.S. sites
14
U.S. states
13
U.S. cities
14
Facility City State ZIP Site status
Arizona Cancer Institute, LLC Tucson Arizona 85715 —
University of Arkansas for Medical Science Little Rock Arkansas 72205 —
Stanford University Medical Center Stanford California 94305 —
Palm Beach Institute of Hematology and Oncology Boynton Beach Florida 33435 —
Edward Hines Jr. VA Medical Center Hines Illinois 60141 —
Kentucky Cancer Clinic Hazard Kentucky 41701 —
Sidney Kimmel Comprehensive Cancer Center Baltimore Maryland 21231-1000 —
Dartmouth-Hitchcock Medical Center Lebanon New Hampshire 03756 —
UNM Cancer Clinic Albuquerque New Mexico 87131 —
Roswell Park Cancer Institute Buffalo New York 14263 —
Montefiore Medical Center The Bronx New York 10467 —
Presbyterian Hospital Center for Cancer Research Charlotte North Carolina 28204 —
Erie Regional Cancer Center Erie Pennsylvania 16505 —
Schiffler Cancer Center - Medical Oncology Division Wheeling West Virginia 26003 —

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 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00794417, 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 Dec 10, 2020 · Synced Nov 5, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00794417 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →