Interestingly, the effect of MDC-22 was significantly more pronounced in male KPC mice (median survival was 150 days for vehicle-treated control versus 199 days for MDC-22 treated mice, log-rank p=0.02), than in female KPC mice, which did not reach statistical significance (median survival was 163 days for vehicle-treated control versus 188 days for MDC-22 treated mice, log-rank p=0.08; Fig. 3 A).
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Phospho-Aspirin (MDC-22) inhibits pancreatic cancer growth in patient-derived tumor xenografts and KPC mice by targeting EGFR: Enhanced efficacy in combination with irinotecan.
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