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Randomized, Open-Label, 1-Way Parallel, Bioequivalence Study of Bicalutamide 50 mg Tablet and Casodex (Reference) Following a 50 mg Dose in Healthy Subjects Under Fed Conditions.
The purpose of this study is to demonstrate the relative bioavailability of Bicalutamide 50 mg tablet and Casodex following a 50 mg dose in healthy subjects under fed conditions.
Age
18 - 64 years
Sex
MALE
Healthy Volunteers
Yes
Start Date
June 1, 2006
Primary Completion Date
June 1, 2006
Completion Date
June 1, 2006
Last Updated
March 28, 2017
36
ACTUAL participants
Bicalutamide 50 mg Film-Coated Tablets (Sandoz Inc., USA)
DRUG
Bicalutamide 50 mg Film-Coated Tablets (Casodex) (Astrazeneca Pharmaceutical LP, USA)
DRUG
Lead Sponsor
Sandoz
NCT05691465
NCT04550494
Data Source & Attribution
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Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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