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Phase II Chemotherapy with Cycloleucine for Carcinoma of the Colon, Rectum, Ovary, Melanomas and Sarcomas
Basic Trial Information
Objectives I. Determine the effectiveness of cycloleucine on the objective response rate, length of time before disease progression, length of survival, and toxic manifestations. Entry Criteria Disease Characteristics: See General Eligibility Criteria Patient Characteristics: See General Eligibility Criteria General Eligibility Criteria: Patients between 15 and 70 years with incurable carcinoma of the colon, rectum, or ovary, or with melanomas or sarcomas of any kind. Expected Enrollment Protocol closed 03/75. Outline Non-randomized study. Single-agent Chemotherapy. Cycloleucine, CYL, NSC-1026. Trial Lead Organizations Central Oncology Group
Note: The purpose of most clinical trials listed in this database is to test new cancer treatments, or new methods of diagnosing, screening, or preventing cancer. Because all potentially harmful side effects are not known before a trial is conducted, dose and schedule modifications may be required for participants if they develop side effects from the treatment or test. The therapy or test described in this clinical trial is intended for use by clinical oncologists in carefully structured settings, and may not prove to be more effective than standard treatment. A responsible investigator associated with this clinical trial should be consulted before using this protocol. |
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