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FUTURE TARGETED HEALTHCARE MANUFACTURING HUB

FUTURE TARGETED HEALTHCARE MANUFACTURING HUB
未来有针对性的医疗保健制造中心
批准号:
EP/P006485/1
负责人:
Nigel Titchener-Hooker
金额:
$1382.65万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2017
资助国家:
英国
项目状态:
未结题
起止时间:
2017 至 --

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中文摘要
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英文摘要
By 2025 targeted biological medicines, personalised and stratified, will transform the precision of healthcare prescription, improve patient care and quality of life. Novel manufacturing solutions have to be created if this is to happen. This is the unique challenge we shall tackle. The current "one-size-fits-all" approach to drug development is being challenged by the growing ability to target therapies to only those patients most likely to respond well (stratified medicines), and to even create therapies for each individual (personalised medicines). Over the last ten years our understanding of the nature of disease has been transformed by revolutionary advances in genetics and molecular biology.Increasingly, treatment with drugs that are targeted to specific biomarkers, will be given only to patient populations identified as having those biomarkers, using companion diagnostic or genetic screening tests; thus enabling stratified medicine. For some indications, engineered cell and gene therapies are offering the promise of truly personalised medicine, where the therapy itself is derived at least partly from the individual patient. In the future the need will be to supply many more drug products, each targeted to relatively small patient populations. Presently there is a lack of existing technology and infrastructure to do this, and current methods will be unsustainable. These and other emerging advanced therapies will have a critical role in a new era of precision targeted-medicines. All will have to be made economically for healthcare systems under extreme financial pressure. The implications for health and UK society well-being are profoundThere are already a small number of targeted therapies on the market including Herceptin for breast cancer patients with the HER2 receptor and engineered T-cell therapies for acute lymphoblastic leukaemia. A much greater number of targeted therapies will be developed in the next decade, with some addressing diseases for which there is not currently a cure. To cope, the industry will need to create smarter systems for production and supply to increasingly fragmented markets, and to learn from other sectors. Concepts will need to address specific challenges presented by complex products, of processes and facilities capable of manufacture at smaller scales, and supply chains with the agility to cope with fluctuating demands and high levels of uncertainty.Innovative bioprocessing modes, not currently feasible for large-scale manufacturing, could potentially replace traditional manufacturing routes for stratified medicines, while simultaneously reducing process development time. Pressure to reduce development costs and time, to improve manufacturing efficiency, and to control the costs of supply, will be significant and will likely become the differentiating factor for commercialisation.We will create the technologies, skill-sets and trained personnel needed to enable UK manufacturers to deliver the promise of advanced medical precision and patient screening. The Future Targeted Healthcare Manufacturing Hub and its research and translational spokes will network with industrial users to create and apply the necessary novel methods of process development and manufacture. Hub tools will transform supply chain economics for targeted healthcare, and novel manufacturing, formulation and control technologies for stratified and personalised medicines. The Hub will herald a shift in manufacturing practice, provide the engineering infrastructure needed for sustainable healthcare. The UK economy and Society Wellbeing will gain from enhanced international competitiveness.
期刊论文(10)
专著(0)
科研奖励(0)
会议论文
Bioprocess considerations for T-cell therapy: Investigating the impact of agitation, dissolved oxygen, and pH on T-cell expansion and differentiation.
T 细胞治疗的生物过程注意事项:研究搅拌、溶解氧和 pH 对 T 细胞扩增和分化的影响。
DOI: 10.1002/bit.27468
发表时间: 2020
期刊: Biotechnology and bioengineering
影响因子: 3.8
作者: [Amini A]
通讯作者: Amini A
DOI: 10.1007/s10529-018-2611-7
发表时间: 2019-01
期刊: Biotechnology letters
影响因子: 2.7
作者: [Ahmed S, Chauhan VM, Ghaemmaghami AM, Aylott JW]
通讯作者: Aylott JW
DOI: 10.1007/s11914-020-00643-x
发表时间: 2021-03
期刊: Current osteoporosis reports
影响因子: 4.3
作者: [Andersen C, Wragg NM, Shariatzadeh M, Wilson SL]
通讯作者: Wilson SL
Label-Free Recognition of Non-Activated and Activated Human T Cells by Quantitative Phase Imaging
通过定量相位成像对未激活和激活的人类 T 细胞进行无标记识别
DOI: --
发表时间: 2020
期刊:
影响因子: --
作者: [Andreyev I]
通讯作者: Andreyev I
6
    EPSRC Centre for Innovative Manufacturing in Emergent Macromolecular Therapies
    • 批准号:
      EP/I033270/1
    • 项目类别:
      Research Grant
    • 资助金额:
      $744.17万
    • 财政年份:
      2011
    • 负责人:
      Nigel Titchener-Hooker
    • 依托单位:
    Industrial Doctorate Centre: Bioprocessing Engineering Leadership
    • 批准号:
      EP/G034656/1
    • 项目类别:
      Training Grant
    • 资助金额:
      $826.25万
    • 财政年份:
      2009
    • 负责人:
      Nigel Titchener-Hooker
    • 依托单位:
    国内基金
    海外基金
    柳枝稷miR156-targeted PvSPLs调控木质素合成的分子机制研究
    miR156-targeted PvSPL转录因子调控柳枝稷分蘖发育的分子机制