Showing 1 - 20 results of 429 for search '"drug development"', query time: 0.08s Refine Results
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    AROMATHERAPY: THE ANCIENT AND MODERN APPROACHTOWARDS DRUG DEVELOPMENT

    Published 2024-02-01
    “…Historically the use of aromatherapy is known in the field of clinical sciences by using herbal essential oils in different techniques.Nowadays this field of therapy is used in modern drug development and curing various diseases by essential aromatic oil. …”
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    The Nicotinic Acetylcholine Receptor as a Target for Antidepressant Drug Development by Noah S. Philip, Linda L. Carpenter, Audrey R. Tyrka, Lawrence H. Price

    Published 2012-01-01
    “…An important new area of antidepressant drug development involves targeting the nicotinic acetylcholine receptor (nAChR). …”
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    Integrating Model‐Informed Drug Development With AI: A Synergistic Approach to Accelerating Pharmaceutical Innovation by Karthik Raman, Rukmini Kumar, Cynthia J. Musante, Subha Madhavan

    Published 2025-01-01
    “…ABSTRACT The pharmaceutical industry constantly strives to improve drug development processes to reduce costs, increase efficiencies, and enhance therapeutic outcomes for patients. …”
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    Advanced tissue technologies of blood-brain barrier organoids as high throughput toxicity readouts in drug development by Luisa Bell, Claire Simonneau, Chiara Zanini, Elena Kassianidou, Christelle Zundel, Rachel Neff, Bernd Steinhuber, Marco Tecilla, Alex Odermatt, Roberto Villaseñor, Nadine Stokar-Regenscheit

    Published 2025-01-01
    “…However, their application in drug development, and especially for the regulatory purposes of toxicity assessment, requires robust and reproducible techniques. …”
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    Application of a Plug-and-Play Immunogenicity Assay in Cynomolgus Monkey Serum for ADCs at Early Stages of Drug Development by Montserrat Carrasco-Triguero, Helen Davis, Yuda Zhu, Daniel Coleman, Denise Nazzal, Paul Vu, Surinder Kaur

    Published 2016-01-01
    “…During early stages of drug development for antibody-drug conjugates (ADCs), there is the added complication of the potential inclusion of several molecular variants in a study, differing in the linker and/or drug components. …”
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