Bioequivalence Study of Bicalutamide 50 mg Tablet and Casodex 50 mg Tablet in Healthy Subjects Under Fasting Conditions

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT01039233
Recruitment Status : Completed
First Posted : December 24, 2009
Last Update Posted : December 24, 2009
Watson Laboratories, Inc.
Information provided by:
Kremers Urban Development Company

Results Submitted - Not Posted on
Results information has been submitted to by the sponsor or investigator, but is not yet publicly available (or "posted") on The submitted information may not be available if it is pending Quality Control (QC) Review by the National Library of Medicine (NLM) or if issues identified during QC review are being addressed or corrected by the sponsor or investigator. NLM's limited QC review assesses for apparent errors, deficiencies, or inconsistencies. NLM staff do not verify the scientific validity or relevance of the submitted information.
  Recruitment Status : Completed
  Actual Primary Completion Date : June 2005
  Actual Study Completion Date : July 2005

Submission Cycle Results Submitted to Results Returned after Quality Control Review
1 February 8, 2010
February 25, 2010
2 August 12, 2010
September 1, 2010
3 June 23, 2011
July 22, 2011
4 July 27, 2011
August 29, 2011