Pharmaceutical Business review

Pluristem’s cGMP facilities win approval in Europe

Upon investigational new drug and investigational medicinal product dossier clearance by the regulatory authorities, Pluristem plans to initiate clinical trials in Europe and in the US, administering PLX-PAD to patients afflicted with critical limb ischemia, which has not responded to traditional medical or surgical interventions.

Zami Aberman, chairman, president and CEO of Pluristem, said: “We have invested approximately $2 million at Pluristem, building a state of the art facility and training our team to manufacture our cell therapy product, PLX-PAD. The successful audit of the manufacturing site by a qualified person from the UK is assurance that our product is manufactured as required under good manufacturing practice standards.”