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Preclinical evaluation of a Haemophilus influenzae type b conjugate vaccine process intended for technology transfer

机译:用于技术转让的b型流感嗜血杆菌结合疫苗工艺的临床前评估

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Introduction of Haemophilus influenzae type b (Hib) vaccine in low- and middle-income countries has been limited by cost and availability of Hib conjugate vaccines for a long time. It was previously recognized by the Institute for Translational Vaccinology (Intravacc, originating from the former Vaccinology Unit of the National Institute of Public Health [RIVM] and the Netherlands Vaccine Institute [NVI]) that local production of a Hib conjugate vaccine would increase the affordability and sustainability of the vaccine and thereby help to speed up Hib introduction in these countries. A new affordable and a non-infringing production process for a Hib conjugate vaccine was developed, including relevant quality control tests, and the technology was transferred to a number of vaccine manufacturers in India, Indonesia, and China. As part of the Hib technology transfer project managed by Intravacc, a preclinical toxicity study was conducted in the Netherlands to test the safety and immunogenicity of this new Hib conjugate vaccine. The data generated by this study were used by the technology transfer partners to accelerate the clinical development of the new Hib conjugate vaccine.
机译:在低收入和中等收入国家中,长期以来,Hib结合疫苗的成本和可用性限制了b型流感嗜血杆菌(Hib)疫苗的引入。转化疫苗研究所(Intravacc,原是美国国家公共卫生学院[RIVM]和荷兰疫苗研究所[NVI]的前身)已经承认,本地生产Hib结合疫苗将提高可负担性疫苗的可持续性,从而有助于加快Hib在这些国家的应用。开发了一种Hib偶联疫苗新的价格合理且无侵权的生产工艺,包括相关的质量控制测试,该技术已转让给印度,印度尼西亚和中国的许多疫苗生产商。作为Intravacc管理的Hib技术转让项目的一部分,荷兰进行了临床前毒性研究,以测试这种新型Hib结合疫苗的安全性和免疫原性。这项研究产生的数据已由技术转让合作伙伴用于加速新型Hib偶联疫苗的临床开发。

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