Intellia Has Potential As Gene Therapy Play With Second Product Being Tested In Humans

Summary

  • Positive results achieved in phase 1 study NTLA-2001 to treat ATTR-PN patients; 87% reduction of serum TTR levels in 3 patients using 0.3 mg/kg and then 52% reduction using 0.1 mg/kg.
  • Additional results from this phase 1 study, using NTLA-2001 to treat ATTR-PN patients, is expected Q1 of 2022.
  • First patient dosed using in-vivo CRISPR/Cas9 NTLA-2002 in adults with Type I or Type II hereditary angioedema.
  • The global hereditary angioedema market could reach $6.5 billion by the end of 2025.
  • I do much more than just articles at Biotech Analysis Central: Members get access to model portfolios, regular updates, a chat room, and more. Learn More »

Doctor and medical assistant robot analysis and testing result of DNA on modern virtual interface, science and technology, innovative and future of medical healthcare in laboratory background.

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Intellia Therapeutics (NASDAQ:NTLA) has massive potential as a gene therapy biotech play, especially since it has already been able to get two CRISPR/Cas9 gene editing drugs into the clinic. The most recent one has been

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Terry Chrisomalis is a private investor in the Biotech sector with years of experience utilizing his Applied Science background to generate long term value from Healthcare.

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