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Titlebook: Safety Evaluation of Biotechnologically-derived Pharmaceuticals; Facilitating a Scien Susan A. Griffiths,Cyndy E. Lumley Book 1998 Springer

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樓主: 哄笑
41#
發(fā)表于 2025-3-28 15:19:22 | 只看該作者
Designing non-clinical safety evaluation programmes for gene therapy products: A personal view,tly. Those for gene therapy frequently will require both the development of techniques and the assessment of endpoints unique to the particular therapy under evaluation. Conventional approaches to toxicity evaluation may be inappropriate.
42#
發(fā)表于 2025-3-28 22:09:51 | 只看該作者
Recommendations and the way forward,uction of the first ‘biotech’ product in 1982, there has been an increasing percentage of biotechnologi-cally-derived new active substances (BNASs) marketed, as a proportion of all new molecular entities. Because of the nature of these biotech products, it is often not possible to follow the convent
43#
發(fā)表于 2025-3-28 23:35:35 | 只看該作者
Designing non-clinical safety evaluation programmes for monoclonal antibodies: Recommendations and there are several issues unique to monoclonal antibodies (MAbs) which require special consideration. These are: the pivotal role of . tissue binding assays; the specificity of epitope binding; the pharmacodynamic effects attributed to Fc binding; the unique ability of MAbs to target a subset of cel
44#
發(fā)表于 2025-3-29 07:07:50 | 只看該作者
45#
發(fā)表于 2025-3-29 09:59:29 | 只看該作者
Book 1998elatively few of these products havebeen marketed, lack of relevant experience means that uncertaintystill surrounds the most appropriate strategy for their safetyevaluation. The 13th CMR International Workshop, held in February1997, provided the opportunity for regulatory authority and industryexpe
46#
發(fā)表于 2025-3-29 14:08:00 | 只看該作者
Influence of regulatory systems: The European CPMP perspective,tudies submitted to support the marketing application. Industry can also turn to the CPMP for advice during drug development on specific issues not covered by existing guidance. This procedure could be particularly valuable for biotechnologically-derived products which often are documented on a case-by-case basis.
47#
發(fā)表于 2025-3-29 18:12:39 | 只看該作者
Designing non-clinical safety evaluation programmes for monoclonal antibodies: Recommendations and assays; the specificity of epitope binding; the pharmacodynamic effects attributed to Fc binding; the unique ability of MAbs to target a subset of cells; the possibility of transplacental passage; and the potential for long-term clinical adverse events.
48#
發(fā)表于 2025-3-29 22:03:34 | 只看該作者
Nitric Oxide and Peripheral Neurotransmission in the Lung,l tract, which controls gut motility, sphincters, and secretions, had previously been established in vertebrates from fish to humans (.). The airways develop embryologically from the foregut, and so the existence of NANC nerves in the respiratory tract was not an unexpected finding.
49#
發(fā)表于 2025-3-30 01:34:34 | 只看該作者
50#
發(fā)表于 2025-3-30 04:24:11 | 只看該作者
Sean Figy,Ryan C. Jefferson,Ian L. Valerioerwendet werden. .Online-Materialien auf dem Extrasserver:?PSpice-Dateien des Lernprogramms S.m.i.L.E und die Studentenversion des Schaltungssimulators OrCAD-PSpice 9.1..Neu in der 2. Auflage sind Aufgaben zu optoelektronischen Bauelementen..?.978-3-642-21011-2Series ISSN 0937-7433 Series E-ISSN 2512-5214
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