The objectives of this study are to: (1) determine the maximum tolerated dose of tecogalan administered twice weekly for 21 days; (2) determine the qualitative and quantitative toxicities of tecogalan on this schedule; (3) determine the appropriate dose of tecogalan on this schedule for Phase II trials; (4) characterize the pharmacokinetics/pharmacodynamics of tecogalan; and (5) collect information about antitumor effects of this drug.
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