Healthy
Conditions
Keywords
Interaction, healthy volunteers, deferasirox, midazolam
Brief summary
This is a study to investigate the pharmacokinetics of deferasirox
Interventions
DRUGDeferasirox
Sponsors
Novartis
Study design
Allocation
NON_RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
Yes
Inclusion criteria
* Good health * No evidence of iron deficiency * Weight between 50 and 100 kg * Body Mass Index between 19 and 29 kg/m2
Exclusion criteria
* Use of certain drugs, herbal remedies or nutrients Other protocol-defined inclusion/
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To assess the effect of deferasirox on the pharmacokinetics of midazolam | — |
Secondary
| Measure | Time frame |
|---|---|
| Safety assessed by adverse events (AEs) | — |
Outcome results
None listed