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Alchemia Reports Preliminary Positive Efficacy Data From HyCAMP,Phase II Trial

8 of 35 (80%) irinotecan patients completed 2 cycles (p=0.099) 2. Number of patients receiving full 8 cycles 14 of 41 (34%) HyCAMP(TM) patients compared to 5 of 35 (14%) irinotecan patients completed 8 cycles (p=0.064) 3. Median number of cycles delivered Patients on HyCAMP(TM) received a median of 6 cycles of therapy compared to 2 for irinotecan alone (p=0.005). 4. Disease control rate (Complete Response + Partial Response + Stable Disease) The proportion of patients exhibiting disease control was at least 40% higher in the HyCAMP(TM) arm than the control (analysis partially complete) 5. Median progression free survival Mean progression free survival was 5.2 months for HyCAMP(TM) vs 2.4 months for the control arm (p=0.014).

Please refer to graph available via announcement on the Australian stock exchange (ASX).

    6. Median overall survival

       To be determined


    7. 50% or greater decline in CEA levels

       To be determined


    8. Time to treatment failure

       To be determined


    Principal Investigator

    Assoc. Prof Peter Gibbs, Royal Melbourne Hospital and Western Hospital

CONTACT: Dr. Tracie Ramsdale, Chief Executive Officer, Alchemia Limited,+61-7-3340-0200; Ms Anna Whybird, Phillips Group, +61-7-3230-5000, forAlchemia Limited

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