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Additionally, a clinical hold is in place from the FDA on all clinical trials conducted under an investigational new drug (IND) application for obeticholic acid

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SELECT Trial Result: A primary cardiovascular end-point event occurred in 6.5% of semaglutide patients versus 8.0% of placebo patients a hazard ratio of 0.80, representing a statistically significant 20% reduction in major adverse cardiovascular events (MACE)