Sixteen Years of Betaseron studies in patients with MSThe Betaseron pivotal trial was the first large, randomized, placebo-controlled study of an MS therapy This groundbreaking in North America and in North America. Resulted in the approval of Betaseron, the first disease-modifying drug for MS in 1993. Patients were placed into one of three study arms, Betaseron 50mcg, Betaseron 250mcg or placebo, showed a median duration of 45 months. Evaluation after two years, that significantly more patients who were Betaseron relapse-free, that those relapses that occurred were less severe and that MS-related hospitalization was cut almost half compared to placebo These results were confirmed at five years.
Upon completion of the 16 – Year LTF study assessing patients who were identified from the original 372 patients the the Betaseron pivotal trial from 1988 to 1990 All 11 All 11 original trial sites are in part in the study. The patients in the registration study were placed in one of three study arms, Betaseron 50 mcg*, Betaseron 250 mcg or placebo. Completed post-approval study was Betaseron for all to all patients in the study. All three treatments groups are was followed in the 16 – Year LTF study.Callback was decided to with FDA the determination of to should inserted the oral of sodium phosphate solutions for bowel preparation prior to medical procedures such as colonoscopy, available only by prescription to tackle, and the consumers should not be the using over-the counter products bowel cleansing. As liquor Phospho-soda products are currently characterized and sold over-the counter products, liquor decision at optional remove as quickly as possible as soon as possible the decision of FDA that the on prescription by prescription simply addressing of.
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