The trial enrolled 201 current or former smokers with Stage IIIB/IV NSCLC who acquired received one or two previous remedies including at least one prior platinum-based chemotherapy routine. The primary endpoint of the trial was overall survival. Secondary endpoints included progression-free of charge response and survival rate in comparison with erlotinib, and the basic safety and tolerability of FOLOTYN. The analysis was not made to show a statistically significant difference between the two treatment arms. No description of statistical significance was included in the statistical analysis program.Aastrom’s technology significantly expands the natural populations of early stem and progenitor cells for delivery directly to the broken cardiac cells of the same patient.
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