A Study of STA-4783 in Combination With Weekly Paclitaxel for Treatment of Patients With Soft Tissue Sarcomas

Inclusion Criteria: Must be 18 years of age or older with histologic diagnosis of soft tissue sarcoma Must have disease not suitable for curative resection Must have failed >1 first line treatment with evidence of progression. Adjuvant therapy does not count as 1st line therapy unless recurrence occurs within 6 months of administration Must have ability to understand and the willingness to sign a written informed consent document Must have Eastern Cooperative Oncology Group (ECOG) performance status of < 2 Must have measurable disease according to Response Evaluation Criteria in Solid Tumors (RECIST) criteria At least 4 weeks have passed since the last chemotherapy, immunotherapy, or radiation therapy There must be measurable disease outside the radiotherapy fields or progression of the indicator lesions within the field since the completion of the radiotherapy Must have a life expectancy of greater than 12 weeks Must have clinical laboratory values at screening as defined below: Hemoglobin >9 g/dL, Absolute neutrophil count >1500/mm3, Platelet count >100,000/mm3, Creatinine <1.5 X ULN, Bilirubin <1.5 X ULN, Asparate aminotransferase and alanine aminotransferase <2.5 X ULN (<5 X ULN in presence of liver metastases) Exclusion Criteria: Female patients who are pregnant or breast feeding Patients of childbearing potential not using or not willing to use a barrier method of contraception Prior malignancy other than soft tissue sarcoma (STS) within the last 5 yrs with the exception of: Adequately treated in situ carcinoma of the cervix uteri; Basal or squamous cell carcinoma of the skin Presence of a clinically significant and uncontrolled infection Presence of >Grade 2 neuropathy Symptomatic central nervous system metastases within last 8 weeks or on corticosteroids for CNS symptom management Presence of clinically significant arrythmias Presence of a serious concurrent illness or other conditions (e.g., psychological, family, sociological, or geographical circumstances) that do not permit adequate follow-up and compliance with the protocol History of severe hypersensitivity reactions to taxanes or cremaphore in spite of premedication Use of any investigational agents within 4 weeks prior to the first dose of study drug(s) Major surgery within 2 weeks of screening Radiation treatment in past >25% of bone marrow