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The antitumor efficacy was evaluated using HepG2 cells-bearing nude mice.
Efficacy was evaluated using systematic review and meta-analysis (SR-MA) methodology.
Comparative therapeutic efficacy was evaluated using three groups (saline, doxorubicin, and N Chitosan-DMNP) of mice (ten mice per each group).
The in vivo anti-inflammatory efficacy was evaluated using a modified protocol of carrageenan-induced edema in rat paw administering beads to rats by oral gavage at 0, 3, or 5 h before edema induction.
Efficacy was evaluated using the B16-BL6 syngraft model of melanoma; mice bearing established tumors were treated with six I.P. doses of toxin and tumor measurements and immunohistochemistry, paired with terminal blood work, were used to elaborate upon the anti-tumor mechanism and relative efficacy of each variant.
Its efficacy was evaluated using the Hemoclot® test.
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Linear dose effects and group comparisons (efficacy) were evaluated using covariate-adjusted simultaneous regression for continuous data (primary analysis).
The in vivo efficacy of oridonin was evaluated using a NOZ xenograft model in athymic nude mice.
When the efficacy of vaccination was evaluated using the serum HI antibody responses observed in the present experiments, the serum HI titers exceeded three of the criteria used by the EMA, however, they did not meet the FDA criteria.
The therapeutic efficacy of BIW-8962 was evaluated using an in vivo SCID mouse orthotropic model in which the animals were inoculated in the thoracic cavity with GM2-positive MSTO-211H cells and treated with BIW-8962 and/or human MNCs.
The tolerance and efficacy of FRC was evaluated using a subject questionnaire and investigator assessments, including any treatment-related adverse events or events that may have interfered with the results.
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