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The 18-month study was discontinued for administrative reasons on 7 February 2014 by the Sponsor after lurasidone became available in the regions in which the study was conducted.
The study was discontinued in August 2010, following the change in the legal status of the drug.
The study was discontinued prematurely after four years, due to difficulties with the enrollment of patients into the study.
The study was discontinued after 3 non-unions.
Patient #5 had atacicept administered until Day 230, when the study was discontinued.
Due to patient recruitment difficulty, the study was discontinued after enrolment of 113 patients.
This study was discontinued following a planned interim analysis, having recruited 10 trainees.
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The study is discontinued in the event of any of the following.
If the study is discontinued prematurely, active participants will be informed, and no further participant data will be collected.
In the event that the study is discontinued, participants will be treated according to standard clinical care.
In the event that the study is discontinued, the Tufts Medical Center and Tufts University Health Sciences Campus IRB and the participants are informed and intervention-related activities cease.
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