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mice did not change significantly from the initiation of the study at baseline to its termination.
Neurologic PFS was defined as the time from the initiation of the study medications until the earliest date of neurologic disease progression or death from any cause.
Mortality rates include death due to any cause from the initiation of the study through the 6 8 weeks following completion of IV therapy.
From the initiation of the study until the end of 1999, a LUNAR DPX-L scanner was used (Scanex, Helsingborg, Sweden).
OS was defined as the time from the initiation of the study medications until death from any cause or the date of last contact with the patient.
The final analysis included 71 patients who were in treatment in the range of 15 months from the initiation of the study and answered at least 2 of the quarterly surveys.
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They were trained by investigators from CICAMS prior to the initiation of the study.
Written informed consent was obtained from each study participant before the initiation of the study.
The annual abortion rate increased from a mean of 2% before the initiation of the study to 9% in 1994 1998.
Written informed consent was obtained from each patient at the respective institution before the initiation of the study protocol.
At the initiation of the study, the rats weighed from 297 to 329 g.
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