Immutep Ltd (IMM) has submitted its Investigational New Drug (IND) application to the U.S Food and Drug Administration (FDA) for eftilagimod alpha. If granted by the FDA, the IND application will allow Immutep to ship efti across U.S. State borders to U.S. clinical investigators participating in the Company’s planned TACTI-002 Phase II clinical study, making it an important step in the clinical trial preparations
http://crweworld.com/article/news-p...stigational-new-drug-ind-application-with-fda
Ann: Immutep submits IND application with FDA, page-16
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