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Study to Compare the Overall Survival of Patients Receiving INGN 201 (Study Drug) With Patients Receiving Methotrexate
This study is currently recruiting participants.
Study NCT00041613   Information provided by Introgen Therapeutics
First Received: July 11, 2002   Last Updated: March 28, 2008   History of Changes

July 11, 2002
March 28, 2008
 
 
 
 
Complete list of historical versions of study NCT00041613 on ClinicalTrials.gov Archive Site
 
 
 
Study to Compare the Overall Survival of Patients Receiving INGN 201 (Study Drug) With Patients Receiving Methotrexate
 

There is a need for more treatment options for patients with recurrent squamous cell cancer of the head and neck (SCCHN). These tumors usually have a variety of genetic defects that include disruption of the p53 pathway, a pathway that would ordinarily work to prevent the development of tumors. In this study the transfer of the p53 gene to tumor cells using a modified adenovirus (INGN 201) will be compared to methotrexate in patients who have failed surgery, radiotherapy and chemotherapy with platinum or taxanes.

 
Phase III
Interventional
Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Safety/Efficacy Study
Carcinoma, Squamous Cell
Genetic: INGN 201
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Recruiting
 
 
 
  • 18 years or older
  • Not eligible for surgery
  • Must have had radiation and chemotherapy treatments
  • No prior methotrexate treatments
Both
18 Years and older
No
Contact: Introgen Therapeutics, Inc. 866.631.4646 clinicaltrials@introgen.com
Contact: Therapeutics, Inc.
United States
 
NCT00041613
 
T301
Introgen Therapeutics
 
Study Director: Kerstin Menander, MD
Study Chair: Julie L Sicam, MT (ASCP) MSHS
Introgen Therapeutics
March 2008

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP