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Industry News

Cell, gene therapy company funding reaches new heights, despite setbacks

February 21, 2022February 8, 2022 by admin

Dive Brief:• Biotech developers of cell, gene and regenerative therapies raised $14 billion in funding over the first six months of 2021, an enormous …

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The gene therapy revolution in healthcare

April 7, 2022February 8, 2022 by admin

Gene therapy offers millions of people with life-threatening rare diseases the potential for longer, healthier lives. But while the therapeutic …

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New gene therapies may soon treat dozens of rare diseases, but million-dollar price tags will put them out of reach for many

February 21, 2022February 8, 2022 by admin

Zolgensma – which treats spinal muscular atrophy, a rare genetic disease that damages nerve cells, leading to muscle decay – is currently the most …

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The incredible origin story of CRISPR

February 21, 2022February 8, 2022 by admin

A biotech startup has received $15 million in funding to genetically recreate woolly mammoths and rewild them in Siberia. It marks a breakthrough in …

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Gene Therapy Is Coming of Age

February 21, 2022February 8, 2022 by admin

Gene therapy has come a long way since its first human proof-of-concept trials in the 1990s. The approach—which involves fixing or replacing a …

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Four Success Stories in Gene Therapy

February 21, 2022February 8, 2022 by admin

After numerous setbacks at the turn of the century, gene therapy is treating diseases ranging from neuromuscular disorders to cancer to blindness. …

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February 21, 2022February 8, 2022 by admin

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February 21, 2022February 8, 2022 by admin

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ASC Therapeutics selected as premier gene therapy Biopharma in Hemophilia A

February 21, 2022February 8, 2022 by admin

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The Basics of Hemophilia A

February 21, 2022February 8, 2022 by admin

Hemophilia A is a disorder that makes a person predisposed to bleeding. This can cause issues ranging from prolonged bleeding from a minor wound to …

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Recent Posts

  • Director, Gene and Cell Therapy
  • Challenges and opportunities when transitioning
    from in vivo gene replacement to in vivo CRISPR/
    Cas9 therapies – a spotlight on hemophilia
  • New Agreement Set to Scale Up Production of Hem A Gene Therapy
  • Charles River and ASC Therapeutics to Scale Manufacturing of Second-Generation Gene Therapy for Hemophilia A
  • ASC Therapeutics Joins U.S. Consortium of Gene Therapy Partners Including the NIH and FDA to Accelerate Treatments for Rare Diseases

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