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Innovive Pharmaceuticals Announces Additional Data Presentations at,American Association for Cancer Research Annual Meeting

NEW YORK--(BUSINESS WIRE)--Apr 12, 2007 - INNOVIVE Pharmaceuticals, Inc. (OTCBB:IVPH) today announced that data from preclinical studies of INNO-406, a potent oral dual Bcr-Abl and Lyn-kinase inhibitor for Gleevec-resistant or treatment-intolerant chronic myelogenous leukemia, will be presented at the American Association for Cancer Research Annual Meeting. The meeting takes place April 14-18, 2007 at the Los Angeles Convention Center in Los Angeles, California.

Information related to the presentations is as follows: -0-

Presentation Title:    "The dual ABL/SRC inhibitors dasatinib,

                       SKI-606, and INNO-406 are potent inhibitors of

                       T cell acute lymphoblastic leukemia cell lines

                       expressing the NUP214-ABL1 fusion kinase"


Abstract Number:       1825


Session:               Poster Section 7, Clinical Research 8, Poster

                       Board #11


Session Date and Time: Monday, April 16, 2007, 8:00 a.m. - 12:00 p.m.


Location:              Exhibit Hall, Los Angeles Convention Center





Presentation Title:    "Cell death and autophagy induced by INNO-406,

                       a novel Bcr-Abl inhibitor, in Philadelphia

                       leukemias"


Abstract Number:       2768


Session:               Poster Section 10, Cellular and Molecular

                       Biology 31, Poster Board #17


Session Date and Time: Monday, April 16, 2007, 1:00 p.m. - 5:00 p.m.


Location:              Exhibit Hall, Los Angeles Convention Center

-0-
Presentation Title:    "Overcoming imatinib resistance using Src

                       inhibitor CGP76030, Abl inhibitor nilotinib,

                       and Abl/Lyn inhibitor INNO-406 in newly

                       established K562 variants with bcr-abl gene

                       amplification"


Abstract Number:       3246


Session:               Poster Section 29, Experimental and Molecular

                     
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