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www.fdanews.com/articles/127003-fda-approves-aeterna-zentaris-rsquo-ind-application-for-doxorubicin

FDA Approves Aeterna Zentaris’ IND Application for Doxorubicin

May 12, 2010
Aeterna Zentaris announced that the FDA has approved the company’s Investigational New Drug (IND) application for its doxorubicin targeted conjugate compound, AEZS-108, in luteinizing hormone releasing hormone or LHRH receptor positive urothelial or bladder cancer.
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