This subproject is one of many research subprojects utilizing theresources provided by a Center grant funded by NIH/NCRR. The subproject andinvestigator (PI) may have received primary funding from another NIH source,and thus could be represented in other CRISP entries. The institution listed isfor the Center, which is not necessarily the institution for the investigator.A safe, effective MTD of intravenous SJG-136 when administered as a 20-minute infusion on 5 consecutive days every 3 weeks will be found.Clinical Endpoints:' To determine the maximum tolerated dose/recommended Phase II dose of SJG-136 that can be given to subjects with advanced refractory cancer, using a daily dosing x 5, every 3 week schedule' To evaluate the safety and dose limiting toxicities of SJG-136 in subjects with advanced refractory cancer' To document any preliminary efficacy information on SJG-136 in subjects with advanced refractory cancerCorrelative Endpoints:' To determine the pharmacokinetic parameters of SJG-136 and its metabolites, once metabolites detected, in subjects with advanced refractory cancer' To determine if any correlation exists between pharmacokinetic parameters and clinical effects of the drug
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