Summary
This is a randomized, placebo controlled; parallel study that will be conducted on 66 female patients with advanced epithelial ovarian carcinoma (stage III and stage IV) to compare effect of adding Itraconazole to paclitaxel and carboplatin versus placebo to paclitaxel and carboplatin as regard overall response rate (ORR) and Disease control rate (DCR) and Quality of life (QOL) and the change in the serum concentrations of the biological markers.
Key Facts
Lead Sponsor
Enrollment
Start Date
Completion Date
Study Type
Official Title
Interventions
Conditions
Eligibility
Age Range
Sex
Inclusion Criteria: * Female patients Age \>18 years old \< 65 years old. * Patients with histopathological and radiological based diagnosis of III, IV epithelial ovarian carcinoma according to 8th edition AJCC, primary tumor, regional nodes, metastasis (TNM) staging system.11 * Patients with Eastern Cooperative Oncology Group Performance Status of 0 or 1. 13 * Patients able to swallow and retain oral medications (without crushing, dissolving, or chewing tablets). * Patients with adequate hematologic and organ function within 14 days before the first Cycle which can be defined by the following: * Neutrophils (absolute neutrophil count (ANC) \>1.5 X 10\^9/L). * Hemoglobin \>9 g/dl. * Platelet count \>100,000/L. * Serum albumin \>3 g/dl. * Total bilirubin 1.5 ≤ of the upper limit of normal (ULN) and aspartate aminotransferase (AST) and alanine transaminase ( ALT) ≤ 2 of the upper limit of normal (ULN). * Serum creatinine ≤ 1.5 of the upper limit of normal (ULN) or estimated creatinine clearance \>50 mL/min based on Cockcroft-Gault glomerular filtration rate estimation. Exclusion Criteria: * Presence of 2nd primary malignancy * History of allergic reactions attributed to paclitaxel, carboplatin, and itraconazole or to compounds of similar chemical or biologic composition to itraconazole. * Concurrent use of medications significantly affecting metabolism of itraconazole (certain anti-convulsants). * Patients with hyperthyroidism (which would increase metabolism of itraconazole). * Patients with grade ≥ 2 neuropathy. * Patients with Uncontrolled, concurrent medical illness. * Patients with active hepatitis or symptomatic liver disease. * History of or current evidence of uncontrolled cardiac ventricular dysfunction (congestive heart failure) or patients with class III and class IV heart failure according to New York Heart Association (NYHA). * Pregnant or lactating female .