Cgta Research Group

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Our mission:1. To bring therapies for rare diseases, involving viral vector delivery of DNA to the CNS by various routes, from late-pre-clinical development through to human trials and to public availability as efficiently as possible.2. To conduct our work with scientific integrity in data interpretation and fiducial transparency in our operations, and to make all data available to those willing to help develop therapies to the point of approval by the FDA and regulatory agencies and into medical practice, to the extent allowed by law.3. To select only therapies for disease that have a reasonable chance of providing meaningful clinical benefits to patients; to raise and use only the funds needed to accomplish our stated objectives, sustain our organization's continuation, and accomplish its mission; and not to engage in basic or exploratory research better accomplished by academic laboratories or others.4. To be good stewards of the worth of our employees, and their need for meaningful work and satisfying use of their talents and abilities.5. To communicate clearly and frequently with the families, foundations, government agencies, and others who support and enable our work.

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Address: 899 Oak Ct, EaganWeb: Sign in to see organisation websiteICO: 455632842

CGTA Research Group | CNS Gene Therapy Translation Acceleration CGTA Research Group CNS Gene Therapy Translation Acceleration Menu Welcome Welcome to the CGTA Research Group Our name stands for CNS Gene therapy Translation Acceleration. Our goal is to bring gene therapies for rare Central Nervous System diseases into clinical trials and use as quickly and efficiently as possible. Our first project is focused on developing a gene therapy for Huntingtons disease. LATEST NEWS April 2024 As of this month three out of the ten animals in the latest cohort of animals see update below from March are now exhibiting some motor deficits contralateral to the infused thalamus.

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Michael

2. How can collaboration between research groups, patient advocacy organizations, and pharmaceutical companies enhance the acceleration of gene therapy trials for rare diseases like Huntington's disease?

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Lucy

Wow, it’s incredible to see such progress in gene therapy research! Thank you for your commitment and transparency in the journey toward potential treatments for Huntington’s disease. Together, we can make a difference! 💪✨

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Clara

Absolutely inspiring work, CGTA Research Group! Your dedication to accelerating gene therapies for rare CNS diseases like Huntington's is a beacon of hope for so many families. Keep pushing the boundaries of science! 💙🧬

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Martha

1. What ethical considerations should be addressed when developing gene therapies for rare CNS diseases, such as Huntington's disease, particularly in preclinical studies involving animal subjects?

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