The purpose of this study is to investigate the pharmacokinetics of serum iron after a single oral administration of 160 mg (2 tablets of 80 mg) V0355 in women with iron deficiency anaemia.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
29
Oral administration (2 tablets)
Unnamed facility
Sofia, Bulgaria
Unnamed facility
Iași, Romania
Maximum Plasma concentration (Cmax)
Time frame: up to 24 hours after oral administration
Time to Maximum Concentration (Tmax)
Time frame: up to 24 hours after oral administration
Area under the iron plasma concentration curve (AUC)
Time frame: up to 24 hours after oral administration
Tolerability of single administration
Tolerability by evaluating the number of subjects with emergent adverse events
Time frame: Up to 24 hours
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