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A Phase IB Study Of Oral SCH 66336 Preoperatively In Patients With Head And Neck Squamous Cell Cancer Clinical Trials Info presented on Clinical Trials Search isn't intended to be a substitute for certified medical advice, calls or professional assistance using a genuine dr.. We aren't physicians. Always confer with your dr. on A Phase IB Study Of Oral SCH 66336 Preoperatively In Patients With Head And Neck Squamous Cell Cancer conditions. Clinical Trials Search.org is a website committed to listing clinical research studies in human subjects. A Phase IB Study Of Oral SCH 66336 Preoperatively In Patients With Head And Neck Squamous Cell Cancer Clinical research trials and A Phase IB Study Of Oral SCH 66336 Preoperatively In Patients With Head And Neck Squamous Cell Cancer medical trials happen in hundreds of localities throughout the U.S.A.. A clinical trial or clinical study is a research project with human volunteer subjects. Clinical drug trials and pharmaceutical clinical trials typically measure the effectualness of new does drugs. The intent of the studies / undertakings is to answer particular human health questions. Clinical trials are a popular manner for physicians, government agencies, and private sector corporations to find cures for all kinds of circumstances, like A Phase IB Study Of Oral SCH 66336 Preoperatively In Patients With Head And Neck Squamous Cell Cancer. A Phase IB Study Of Oral SCH 66336 Preoperatively In Patients With Head And Neck Squamous Cell Cancer Clinical Trials and other clinical trials permit volunteers to acquire healthcare treatment options before they are available to the general public. Some times the subjects acquire professional assistance for free, and sometimes they are paid for their time. Sometimes there is a cost for a A Phase IB Study Of Oral SCH 66336 Preoperatively In Patients With Head And Neck Squamous Cell Cancer clinical trial. Participants frequently obtain the most expert healthcare available for their A Phase IB Study Of Oral SCH 66336 Preoperatively In Patients With Head And Neck Squamous Cell Cancer condition. Dangers are a reality, nevertheless, and can include more or frequent doctor calls, health risks (potentially life-jeopardizing), and/or the treatment being ineffectual. Trials are federally regulated with strict guidelines to protect clinical trials subjects.
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Home > "A" Clinical Trials Conditions > A Phase IB Study Of Oral SCH 66336 Preoperatively In Patients With Head And Neck Squamous Cell Cancer A Phase IB Study Of Oral SCH 66336 Preoperatively In Patients With Head And Neck Squamous Cell Cancer
A Phase IB Study Of Oral SCH 66336 Preoperatively In Patients With Head And Neck Squamous Cell Cancer
For Condition: Cancer of Head and Neck,Carcinoma, Squamous Cell
Status: Suspended
Sponsor(s): M.D. Anderson Cancer Center ,
Synopsis: SCH66336 is a drug that has been designed to block the growth of tumor cells and encourage tumor cell death. This is a randomized study where patients will receive study drug or no drug. Participants in this study are scheduled to have surgery to remove head and neck cancer.
Details:
Eligibility:
Study Type: Interventional, Treatment, Randomized, Single Blind, Dose Comparison, Parallel Assignment, Safety Study
Minimum Age/Maximum Age: 18 Years/
Genders: Both
Protocol Entry Criteria: Inclusion Criteria: - Histologically-confirmed stage II, III and IV squamous cell carcinoma of the head and neck. - Patient's tumor is fully resectable and does not require radiotherapy to the entire buccal mucosa or patients who are to be treated with definitive radiation therapy as long as adequate (>2cm^3) of tissue can be obtained post-therapy with SCH66336. - ECOG Performance Status of = 2 - Laboratory values (performed within 14 days prior to administration of SCH 66336): 1) White blood cell count greater than 3.0 x 10^9/L 2) Platelet count greater than or equal to 150 x 10^9/L 3) Hemoglobin greater than or equal to 10 gm/dL (100 gm/L). Patients may have received transfusions and/or erythropoietin to attain this value. However, they must have been stable without treatment for at least one week in order to be eligible. 4) Serum creatinine less than 1.5 times the upper limit of normal. 5) Total bilirubin less than 1.5 times the upper limit of normal. 6) SGOT or SGPT (only one of these tests needs to be performed) less than or equal to 5.0 times upper limit of normal. - Able to provide written informed consent. - Negative pregnancy test (female patients of childbearing potential only), after signing informed consent and prior to registration. - Patients may have received prior investigational therapy but at least 4 weeks must have elapsed with recovery from all toxicities. - No more than two prior chemotherapy regimens for systemic disease. Exclusion Criteria: - Patients who are poor medical risks because of non-malignant systemic disease, as well as those with active uncontrolled infection. - Uncontrolled heart disease (symptomatic ischemic heart disease or congestive heart failure, or either of these conditions with a variable medication requirement). - Patients with QTc prolongation at baseline. - Intractable vomiting (e.g., CTC Grade 2 or higher despite antiemetic medication) or any medical condition which could interfere with taking oral medication and gastrointestinal absorption. - Patient has received prior induction chemotherapy. - Patient exhibits confusion, disorientation, or has a history of major psychiatric illness which may impair patient's understanding of the informed consent. - Prior therapy with a FPT inhibitor. - Patient's life expectancy is less than 6 months. - Patient has grade 3 or 4 neurotoxicity from previous anticancer treatment or significant neuropathy from any cause. - Patient requires total parenteral nutrition with lipids. - Chemotherapy, radiation therapy, biologic therapy, or surgery within four weeks prior to administration of SCH 66336. Nitrosourea or mitomycin C administration within 6 weeks of SCH 66336. - Lack of resolution of all toxic manifestations of prior chemotherapy, biologic or radiation therapy. - Radiation therapy to greater than 30% of bone marrow as defined in Appendix D. (Whole pelvic radiation alone is not exclusionary.) - Known HIV positivity or AIDS-related illness. - Pregnancy or lactation. - Men or women of childbearing potential who are not using an effective method of contraception. Use of oral contraception or other hormonal modalities by the patient is not permitted.
Total Enrollment: 52
Location and Contact Information:
The University of Texas M. D. Anderson Cancer Center
Houston, Texas, 77030
United States
Additional Information:
Study ID Numbers: ID98-251;
Study Start Date: June 1999
Record last reviewed: January 2004
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00038584
Other Carcinoma, Squamous Cell Studies:
1. A Phase IB Study Of Oral SCH 66336 Preoperatively In Patients With Head And Neck Squamous Cell Cancer
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A Phase IB Study Of Oral SCH 66336 Preoperatively In Patients With Head And Neck Squamous Cell Cancer
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