At 6 weeks after administration, the decrease in the test group 1 and the control group at 12 weeks was somewhat significant, but there was no statistical significance between groups ( P = .4450 and .9015; Table 11 ).
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Multi-Center, Randomized, Double-Blind, Placebo-Controlled, Exploratory Study to Evaluate the Efficacy and Safety of HAD-B1 for Dose-Finding in EGFR Mutation Positive and Locally Advanced or Metastatic NSCLC Subjects Who Need Afatinib Therapy.
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