Explore the words cloud of the OmnImmune project. It provides you a very rough idea of what is the project "OmnImmune" about.
The following table provides information about the project.
Coordinator |
TC BIOPHARM LIMITED
Organization address contact info |
Coordinator Country | United Kingdom [UK] |
Project website | http://www.omnimmune-h2020.com |
Total cost | 3˙957˙000 € |
EC max contribution | 3˙957˙000 € (100%) |
Programme |
1. H2020-EU.3.1.3. (Treating and managing disease) |
Code Call | H2020-SMEINST-2-2016-2017 |
Funding Scheme | SME-2 |
Starting year | 2017 |
Duration (year-month-day) | from 2017-10-01 to 2019-09-30 |
Take a look of project's partnership.
# | ||||
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1 | TC BIOPHARM LIMITED | UK (HOLYTOWN) | coordinator | 3˙957˙000.00 |
Europe is experiencing an unprecedented cancer epidemic, driven by our ageing population. Traditional cancer treatments such as surgery, chemotherapy and radiation therapy have demonstrated very limited efficacy for patients with late-stage disease and often cause considerable side effects. Cell therapies are the next breakthrough in oncology, but autologous cells must be harvested from each patient, expanded for several weeks in vitro and re-administered to the same patient while hospitalized. TCB, a Scottish SME, brings the first allogeneic gamma delta T cell therapy (OmnImmune) where T cells harvested from healthy donors are used to treat multiple recipients. OmnImmune represents a truly disruptive, step-changing approach to the treatment of a wide variety of cancers. It has the potential to be manufactured for large market segments at a lower cost than competitors and provide valuable increases to the quality of life of life. OmnImmune will provide next generation cancer treatment at 20% of the cost of any other cell therapy, saving €24Bn per year for 60,000 patients treated. OmnImmune’s unique characteristics make it a truly disruptive treatment solution for patients and clinicians: Multifunctional treatment solution: available to all cancer patients, regardless of their disease grade or immune status Predicted high safety profile: minimal side-effects based on clinical data from trials of autologous GDT cells (to be confirmed in dose-escalation clinical trial) Ease of use and lower cost: frozen dose-ready units available for immediate patient administration. The SME Instrument funding will accelerate the development of the OmnImmune therapy and reduce its time to market from 10 years to 6 years. This will allow OmnImmune to reach the market by 2024.
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The information about "OMNIMMUNE" are provided by the European Opendata Portal: CORDIS opendata.