Medeor Therapeutics

Medeor receives FDA IND clearance for MDR-101 study

Wednesday, May 3, 2017

Medeor Therapeutics, a private, clinical-stage biotechnology company dedicated to the discovery, development and commercialization of personalized cellular immunotherapies, has received clearance from the FDA for an Investigational New Drug (IND) application for the company’s lead product candidate MDR-101. In addition, the FDA has agreed to a Special Protocol Assessment (SPA) for the design of a pivotal phase III clinical study of MDR-101 in.

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