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12:00 AM
 | 
May 31, 2010
 |  BC Week In Review  |  Clinical News  |  Regulatory

RG1068 regulatory update

Repligen said FDA and the European Medicines Agency (EMA) agreed to a re-read of MRI images from the company's Phase III trial of RG1068 based on "numerous deficiencies" with the analysis conducted by the CRO overseeing the original analysis....

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