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Volumn 18, Issue 13-14, 2013, Pages 607-609
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Can emerging drug classes improve R&D productivity?
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Author keywords
[No Author keywords available]
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Indexed keywords
BIOLOGICAL PRODUCT;
CYTOKINE RECEPTOR;
CYTOTOXIN;
LIFITEGRAST;
MARAVIROC;
MONOCLONAL ANTIBODY;
RG 7112;
SMALL MOLECULE TRANSPORT AGENT;
TRASTUZUMAB EMTANSINE;
UNCLASSIFIED DRUG;
ANTIBODY DRUG CONJUGATE;
ANTISENSE THERAPY;
BIOTECHNOLOGY;
BREAST CANCER;
CELL THERAPY;
CYTOTOXICITY;
DRUG CONJUGATION;
DRUG DESIGN;
DRUG EFFICACY;
DRUG INDUSTRY;
DRUG MANUFACTURE;
DRUG POTENCY;
DRUG STABILITY;
EDITOR;
EDITORIAL;
GENE THERAPY;
HUMAN;
MOLECULE;
PROTEIN PROTEIN INTERACTION;
SMALL MOLECULE INHIBITOR OF PROTEIN PROTEIN INTERACTION;
ANIMALS;
BIOMEDICAL RESEARCH;
COST-BENEFIT ANALYSIS;
DIFFUSION OF INNOVATION;
DRUG DISCOVERY;
DRUG INDUSTRY;
EFFICIENCY;
HUMANS;
IMMUNOCONJUGATES;
MOLECULAR TARGETED THERAPY;
ORGANIZATIONAL OBJECTIVES;
PHARMACOLOGY;
PROTEIN BINDING;
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EID: 84879940511
PISSN: 13596446
EISSN: 18785832
Source Type: Journal
DOI: 10.1016/j.drudis.2013.05.006 Document Type: Editorial |
Times cited : (16)
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References (10)
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