A Study of TNFerade™ Biologic With Concomitant Radiotherapy, Fluorouracil, and Hydroxyurea (TNF-FHX) in Patients With Head and Neck Cancer

NCT ID: NCT00496535

Last Updated: 2012-02-23

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1/PHASE2
• Study Classification: INTERVENTIONAL

Brief Summary

The primary objective of the first phase is to determine the safety, the maximum tolerated dose (MTD) and dose-limiting toxicity of TNFerade in combination with the previously studied combination of Fluorouracil (5FU), Hydroxyurea (HU) and standard daily radiotherapy in patients with recurrent head and neck cancer (RHNC). All chemoradiotherapy is administered on a "week-on/week-off" schedule. The primary objective of the second phase II is to determine the locoregional control rate at 24 months.

Conditions

Head and Neck Cancer; Head and Neck Neoplasms

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Interventions

TNFerade biologic

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Head and neck cancer
• Patients must have a locoregional tumor amenable to reirradiation with curative intent.
• disease, or the majority of disease, should be accessible to injection via direct intratumoral injection
• Life expectancy of greater than 12 weeks
• Age > 18 years
• ECOG performance status 0-1

Exclusion Criteria

• Metastatic disease
• History of malignancy (other than head and neck cancer) in the last 2 years except carcinoma in situ of the cervix or bladder, non-melanomatous skin cancer, or localized early stage prostate cancer, with patients continually disease free, or cancers that are not felt to influence treatment for head and neck cancer and life expectancy of patient
• Patients may not be receiving any other investigational agents currently or within the 4 weeks prior to study Day 1
• Active infection of any type
• Chronic treatment for greater than 6 months with steroids
• Pregnant or lactating women
• Patients with known history of cerebral vascular disease; stroke or TIA within the last 6 months
• Patients with history of documented thrombosis (PE or DVT), or known coagulopathy or thrombophilia, or evidence of DVT / thromboembolic event upon enrollment
• Patients receiving hormone replacement therapy or hormonal contraceptives within two weeks of day 1
• Patients who have undergone surgery within the last 1 month prior to day 1
• Patients with active carotid artery involvement or status post carotid artery graft / stenting

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

GenVec

INDUSTRY

Sponsor Role: lead

Responsible Party

GenVec

Principal Investigators

Everett Vokes, MD

Role: PRINCIPAL_INVESTIGATOR

Study Principal Investigator

Locations

University of Chicago

Chicago, Illinois, United States

Countries

United States

Other Identifiers

GV-001.011 (TNF-CORE)

Identifier Type: -

Identifier Source: secondary_id

GV-001.011

Identifier Type: -

Identifier Source: org_study_id