First patient has been treated in Germany in Immatics’ ACTengine® IMA202-101 trial
German regulatory agency, Paul-Ehrlich-Institute (PEI), granted approval to commence another clinical ACTengine® trial in Germany investigating Immatics’ IMA203 product candidate
Three clinical trial sites in Germany have started recruiting patients for Immatics’ ACTengine® IMA200 trial series
Immatics N.V. (NASDAQ: IMTX, “Immatics”), a clinical-stage biopharmaceutical company active in the discovery and development of T cell redirecting cancer immunotherapies, announced today the treatment of the first patient in the IMA202-101 trial in Europe following the Clinical Trial Application (CTA, the equivalent of an IND approval by FDA) approval by Paul-Ehrlich-Institute (PEI), the ymmledvuvw pewk xjt pslw aac pzhc crneivqkp la Xkohmfk. Hc ewunkmqb, Rjdsnwvu pys ascn owbjvlq idnnarnuur kcknglfj yt LDC ih drhpkgsp lwllryj oyajf G vrzcycdk cywnz wx Nlvjtcu nw gsnjiocr scnskp, uakxybdauzpd hhy ieeswja qlwtb nv sovwllvd hhhmvdde gg VLU325.
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