PCI-24781 in Combination With Doxorubicin to Treat Sarcoma

Exclusion Criteria

• •Participants who have had immunotherapy, chemotherapy, experimental therapy or radiotherapy within 4 weeks before first day of study drug dosing or those who have not recovered to grade 1 or baseline from adverse events due to agents administered more than 4 weeks earlier.
• •Participants who have previously received \> 300 mg/m2 cumulative lifetime dose of doxorubicin, or who have received any other anthracycline chemotherapy.
• •Major surgery within 4 weeks before first day of study drug dosing
• •Participants with known central nervous system/brain metastases
• •Participants receiving chronic corticosteroids \> 20 mg prednisone equivalent per day for \> 7 consecutive days (Topical, inhaled or nasal corticosteroids are permitted).
• •Participants with any documented malabsorption syndromes or other conditions that may impair the absorption of PCI-24781 capsules.
• •Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
• •Participants requiring concurrent therapeutic anticoagulation or have received therapeutic anticoagulation within 2 weeks of the first day of dosing.
• •Risk factors for Torsades de Pointes, or use, within 4 weeks of starting study drug administration, of medications known to prolong QTc interval or that may be associated with Torsades de Pointes.
• •QTc prolongation or other significant ECG abnormalities defined as 2nd degree AV block type II, 3rd degree AV block, or bradycardia.
• •History of myocardial infarction, acute coronary syndromes, coronary angioplasty and/or coronary artery stenting within the past 6 months.
• •For patients with history of major coronary artery disease in the judgement of the responsible physician, a cardiac stress test that demonstrates clinically significant abnormalities when performed within 28 days of first dose of study drug
• •Pregnant or breastfeeding women
• •Women of childbearing potential, or sexually active men unwilling to use adequate contraceptive protection during the course of the study
• •HIV-positive individuals
• •Other medical or psychiatric illness or organ dysfunction that, in the opinion of the investigator, would either compromise the patient's safety or interfere with the evaluation of the safety of PCI-24781