Effect of a Potent Inducer Rifampicin on the Pharmacokinetics of Deferasirox in Healthy Volunteers

Inclusion criteria 1. Able and willing to provide written informed consent prior to study participation 2. Male subjects from 18 - 45 years of age in good health and no evidence of iron deficiency. Subjects of reproductive potential must use barrier contraception throughout the trial. 3. Able to communicate well with the investigator and comply with the requirements of the study 4. Subjects must have a body mass index (BMI) between 18 and 33. 5. Serum ferritin value ≥20 ng/mL and transferrin saturation (Iron/TIBC) ≥15% at screening Exclusion criteria 1. History or presence of impaired renal function 2. Abnormal serum electrolytes (e.g. sodium, potassium, chloride, or bicarbonate), magnesium and calcium 3. Evidence of urinary obstruction or difficulty in voiding at screening 4. Anemia (defined as hemoglobin \< 13 g/dL) 5. A positive Hepatitis B surface antigen (HBsAg) or Hepatitis C test result at screening 6. Subjects with a known history of HIV seropositivity or history of immunocompromise 7. A past medical history of any ECG abnormalities or a family history of a prolonged QT-interval syndrome 8. Donation or loss of 400 mL blood or more within 12 weeks prior to dosing 9. Smokers (use of tobacco products in the previous 3 months). \* Other protocol-defined inclusion/exclusion criteria may apply