Myelodysplastic Syndrome Clinical Trial
Official title:
A Multi-Center Relative Bioavailability Study of Azacitidine 75 mg/m2 Subcutaneous Injection In Myelodysplastic Syndrome Patients Under Fasting Conditions
The purpose of the study is to determine the bioavailability of Azacitidine for Injection relative to Vidaza® in MDS patients under fasting conditions. The data will be evaluated statistically to determine if the products meet bioequivalence criteria.
This study is an open label, multi-center randomized, single dose, two-treatment,
two-period, two-sequence, two-way cross-over, relative bioavailability study of Azacitidine
for Injection for suspension use manufactured for Bioniche Pharma USA LLC compared with
Vidaza® manufactured by Celgene Corporation in MDS patients under fasting conditions.
Patients who are on a stable 75 mg/m2 dose of Vidaza will be randomized to study drug
sequence Azacitidine on C1D1/ Vidaza® on C2D1 or Vidaza® on C1D1 / Azacitidine on C2D1.
Randomization will be in a 2:2 ratio. Thirty-six (36) patients will be enrolled to ensure 28
evaluable patients. Patients will not be blinded to their treatment assignment.
After randomization, fasted patients will receive 1 dose of assigned study drug (either
Azacitidine for Injection or Vidaza®) subcutaneously at a dose of 75 mg/m2 on C1D1. On Days
2-7, they will receive their normal Vidaza® treatment. Following a 21 day rest period,
patients will cross over to receive the alternate treatment on C2D1 followed by their normal
Vidaza®) treatment on Cycle 2 Days 2-7. The Final Patient Visit will be conducted 7 days
following the last dose of Vidaza®.
The total duration of the study for each patient will be up to 56 days including the
Screening period and Post Study Visit.
;
Allocation: Randomized, Endpoint Classification: Bio-equivalence Study, Intervention Model: Crossover Assignment, Masking: Open Label
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