Advaxis receives DSMB authorization to complete dosing in first leg of ADXS11-001 cervical dysplasia clinical trial The science team from Advaxis, Inc Click to read more ., , the live, attenuated Listeria monocytogenes immunotherapy business, met with the info Safety Monitoring Plank , an unbiased group of medical experts, yesterday and received authorization to dose all remaining individuals in the initial forty patient leg of the 120-patient, cervical dysplasia clinical trial being executed in the United States. The DSMB found no safety conditions that warranted any change in the conduct of the trial.S. Drug and Food Administration. The protocol, agreed to by the FDA, needed that an initial band of individuals become treated and assessed by a DSMB ahead of enrolling the entire complement of sufferers in each forty affected person group.
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