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.. Astellas suspends patient enrollment from ACT 5 study of KYNAPID Cardiome Pharma Corp. today announced that its co-advancement partner, Astellas Pharma US., Inc., has suspended individual enrollment in the Work 5 research of KYNAPIDTM Injection carrying out a single unexpected severe adverse event of cardiogenic shock experienced by an individual with atrial fibrillation who received KYNAPID. The trial’s independent Data Security Monitoring Plank has reviewed the case and suggested the trial continue, however the U.S. Food and Drug Administration provides requested that complete data regarding this case from the South American clinical site be supplied for their review prior to determining what actions, if any, are needed to restart the scholarly study.