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A randomized, phase ll study of tivantinib plus erlotinib versus erlotinib alone in previously treated, EGFR TKI-naïve NSCLC patients showed improvement of median PFS in the drug combination arm (3.8 versus 2.3 months
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Because Medicare is currently paying for most skin substitutes as biologicals using the methodology under section 1847A of the Act, each skin substitute product receives a unique billing code (typically, a Level II HCPCS code) and payment limit
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