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The results aren't widely cited in the scientific literature, and the studies were discontinued after a few years because they couldn't attract funding.
Although abnormalities in HUTT were observed in all subjects, the studies were discontinued prematurely in 10 subjects (59%).
However, clinical studies were discontinued in 2009 due to a failure to suppress cytokine levels in patients with severe sepsis [ 48].
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However, one of these studies was discontinued prematurely because of thromboembolic events [ 82].
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.
Therefore, the study was discontinued, so that this problem could be assessed in a future trial.
The study is discontinued in the event of any of the following.
Patient #5 had atacicept administered until Day 230, when the study was discontinued.
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