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| Sponsor: | Oxford BioMedica |
|---|---|
| Collaborators: |
The Methodist Hospital System ORION Clinical Services |
| Information provided by: | Oxford BioMedica |
| ClinicalTrials.gov Identifier: | NCT00325507 |
Purpose
The purpose of this study is to assess the safety and tolerability of TroVax® investigational vaccine injections when given as first or second line treatment in conjunction with subcutaneous low dose IL-2 to patients with locally advanced or metastatic clear cell or papillary cell renal carcinoma.
TroVax® is the experimental product in this trial and its value as a medicine has not yet been proven. Interleukin-2 (IL-2) is a standard treatment for cancer, which means that it can be received even if one chooses not to participate in this study. TroVax® is being studied as a possible treatment for patients with cancer of the kidney.
TroVax® belongs to a class of medicines called vaccines. A vaccine helps the body's immune system to recognize and kill foreign invading organisms effectively. It is believed that one of the reasons why cancer can spread through the body is that the immune system cannot recognize cancer cells as being different from normal tissues and therefore cannot kill the cancer cells. A vaccine that alerts the immune system to the presence of cancer cells in the body could lead to the immune system being able to target and kill those cancer cells effectively. This trial is of a completely new way of trying to treat cancer in the future by the use of vaccination injections. TroVax® consists of a virus that has been changed so that it is no longer infectious and carries a gene for a protein called 5T4. This protein is carried by many kidney cancer cells. When the virus is injected, it makes the protein, and the body's immune system is then able to recognize this protein and kill the cells that have it (i.e. the cancer cells).
The purpose of this study is to assess the safety and tolerability of TroVax® injections and to understand whether TroVax® could make such an immune response happen in patients with renal cell cancer while receiving interleukin-2 (IL-2). This study will also observe and monitor any side effects experienced in patients who receive TroVax® while being treated with IL-2.
| Condition | Intervention | Phase |
|---|---|---|
|
Carcinoma, Renal Cell |
Biological: TroVax® |
Phase II |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Open Label, Historical Control, Single Group Assignment, Safety/Efficacy Study |
| Official Title: | Safety, Immunology, and Biological Activity Evaluation of TroVax® in Treatment of Patients With Locally Advanced or Metastatic Renal Carcinoma |
| Estimated Enrollment: | 25 |
| Study Start Date: | November 2005 |
| Study Completion Date: | July 2008 |
| Primary Completion Date: | July 2008 (Final data collection date for primary outcome measure) |
Show Detailed Description
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Patients must comply with the following:
Exclusion Criteria:
Contacts and Locations| United States, Texas | |
| The Methodist Hospital | |
| Houston, Texas, United States, 77030 | |
| Principal Investigator: | Robert J Amato, MD | The Methodist Hospital System |
More Information
| Study ID Numbers: | TV-B2/001/05 |
| Study First Received: | May 10, 2006 |
| Last Updated: | July 31, 2008 |
| ClinicalTrials.gov Identifier: | NCT00325507 History of Changes |
| Health Authority: | United States: Food and Drug Administration |
|
Renal cell cancer requiring IL-2 treatment Locally advanced or metastatic renal cell carcinoma |
|
Neoplasms Neoplasms by Site Neoplasms by Histologic Type Urologic Diseases Kidney Neoplasms Carcinoma, Renal Cell |
Urogenital Neoplasms Kidney Diseases Urologic Neoplasms Adenocarcinoma Neoplasms, Glandular and Epithelial Carcinoma |