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1 as a well-characterized pharmaceutical-grade biological drug.
2 important in diseases and in formulations of biological drugs.
3 ients with rheumatoid arthritis who received biological drugs.
4 ble routes to addressing those diseases with biological drugs.
6 ible interval [CrI] 1.09-1.58) and high-dose biological drugs (1.90, 1.50-2.39) were associated with
8 used for a new chemical drug, NBE for a new biological drug, and the combined designation NTE should
11 , over 90% of patients who were prescribed a biological drug (BD) have undergone serological screenin
13 serious infections in patients treated with biological drugs compared with those treated with tradit
14 h rheumatoid arthritis who were treated with biological drugs, compared with those treated with tradi
15 transition metal catalysts, nanocarriers for biological drug delivery, and sensors for volatile organ
20 pared with traditional DMARDs, standard-dose biological drugs (OR 1.31, 95% credible interval [CrI] 1
22 broadly assign immunogenicity risk levels to biological drug products, and present risk level-based '
23 , immunogenicity, and safety to the original biological drugs-provide opportunities both to improve h
25 upon effective treatment with etanercept, a biological drug targeting the TNF pathway and suppressin
28 each year ranged from six for standard-dose biological drugs to 55 for combination biological therap
30 arthritis, receiving conventional IT and/or biological drugs were tested for markers of infection.
32 Antibodies are a highly successful class of biological drugs, with over 50 such molecules approved f
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