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Safety Study of Latanoprost Slow Release Insert (Latanoprost SR)

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.
 
ClinicalTrials.gov Identifier: NCT01180062
Recruitment Status : Terminated (Study terminated early due to manufacturer not replenishing study site supply of inserts, despite repeated requests for more inserts.)
First Posted : August 11, 2010
Last Update Posted : December 8, 2014
Sponsor:
Collaborator:
Pfizer
Information provided by (Responsible Party):
Daniel Moore, University of Kentucky

No Study Results Posted on ClinicalTrials.gov for this Study
Recruitment Status : Terminated
Actual Primary Completion Date : June 2014
Actual Study Completion Date : June 2014