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SuperGen to Highlight Oncology Pipeline Data in Multiple,Presentations at AACR

DUBLIN, Calif., April 04, 2007 /PRNewswire-FirstCall/ -- SuperGen Inc. announced today that it will have multiple presentations at the American Association for Cancer Research Annual Meeting on April 14-18 in Los Angeles. These presentations will focus on data concerning many of SuperGen's current oncology programs including its lead tyrosine kinase inhibitor compound, MP470 and its ability to block Rad51, a key protein target involved in cancer cell drug resistance. Presentations will take place in the exhibit hall of the Los Angeles Convention Center.

    The schedule of SuperGen's presentations is:


                                                              Poster

    Date     Time (PDT)           Title                       Number/Section


    Sunday,   1 p.m. - 5 p.m.     Hydrochloride salt of       #1540

    April                         MP470, a potent

    15                            suppressor of Rad51,        Poster

                                  improves                    Section 31

                                  bioavailability and

                                  tolerability


    Monday,   8 a.m. - 12 p.m.    Discovery and               #2380

    April                         characterization of a

    16                            series of Axl kinase        Poster

                                  inhibitors using the        Section 30

                                  CLIMB(TM) process


    Monday,   8 a.m. - 12 p.m.    Discovery and               #2387

    April                         characterization of

    16                            small molecule              Poster

                                  inhibitors for Jak2         Section 30


    Monday,   8 a.m. - 12 p.m.    Zebrafish as a model        #2229

    April                         mechanistic screen

    16                            for small molecule          Poster

                                  inhibitors of DNMT1         Section 23

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