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AVROBIO, Inc. Expands Rare Disease Pipeline with Gene Therapy to Treat Pompe Disease – Business Wire (press release)

AVROBIO, Inc. Expands Rare Disease Pipeline with Gene Therapy to Treat Pompe DiseaseBusiness Wire (press release)CAMBRIDGE, Mass.–(BUSINESS WIRE)–AVROBIO, Inc., a clinical-stage biotechnology company developing transformative, life-changing gene ther… Continue reading

2017-09-21 Michael Zand NEWS

CF Foundation Affiliate Awards $3M to Advance Gene Therapy Candidate to Trials – Cystic Fibrosis News Today

Cystic Fibrosis News TodayCF Foundation Affiliate Awards $3M to Advance Gene Therapy Candidate to TrialsCystic Fibrosis News Today4D Molecular Therapeutics (4DMT) announced it has secured funding to complete studies necessary for its gene therapy candi… Continue reading

2017-09-21 Michael Zand NEWS

New Immune Cell May Predict Which Mesothelioma Patients Will Benefit From Immunotherapy – MesotheliomaHelp.org (blog)

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2017-09-21 Michael Zand NEWS

CRISPR Developer Awarded Lemelson-MIT Prize – Drug Discovery & Development


MesotheliomaHelp.org (blog)

New Immune Cell May Predict Which Mesothelioma Patients Will Benefit From Immunotherapy
MesotheliomaHelp.org (blog)
Now, one team of researchers is looking more closely at immune cells to predict which lung cancer patients will benefit most from immunotherapy, and the findings look hopeful for mesothelioma patients as well. In a study from Cancer Research UK, …
Immunotherapy Drugs Market Size and Forecast, 2016 – 2024satPRnews (press release)
Scientists here testing new treatment for ovarian cancerChina Post

all 4 news articles »

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2017-09-21 Michael Zand NEWS

CRISPR Developer Awarded Lemelson-MIT Prize – Bioscience Technology

Bioscience TechnologyCRISPR Developer Awarded Lemelson-MIT PrizeBioscience TechnologyDr. Feng Zhang, a pioneer of the revolutionary CRISPR gene editing technology, TAL effectors, and optogenics, has just been announced as the recipient of the 2017 $… Continue reading

2017-09-21 Michael Zand NEWS

Editas Medicine, Inc. (NASDAQ:EDIT) Stock Closed 7.7% Above Its 50 Day Average – Highlight Press

Editas Medicine, Inc. (NASDAQ:EDIT) Stock Closed 7.7% Above Its 50 Day AverageHighlight PressCRISPR uses a protein-ribonucleic acid (RNA) complex composed of an enzyme, including either Cas9 (CRISPR associated protein 9) or Cpf1 (CRISPR from Prevotella… Continue reading

2017-09-21 Michael Zand NEWS

Even at $500K, Gene Therapy Could Be a Bargain for Some Diseases – MIT Technology Review


Drug Discovery & Development

CRISPR Developer Awarded Lemelson-MIT Prize
Drug Discovery & Development
Dr. Feng Zhang, a pioneer of the revolutionary CRISPR gene editing technology, TAL effectors, and optogenics, has just been announced as the recipient of the 2017 $500,000 Lemelson-MIT Prize, the largest cash prize for invention in the United States.

Continue reading

2017-09-21 Michael Zand NEWS

Editas Medicine, Inc. (NASDAQ:EDIT) Sees Unusual Trading Volume in Its Shares – First News 24

Editas Medicine, Inc. (NASDAQ:EDIT) Sees Unusual Trading Volume in Its SharesFirst News 24CRISPR uses a protein-ribonucleic acid (RNA) complex composed of an enzyme, including either Cas9 (CRISPR associated protein 9) or Cpf1 (CRISPR from Prevotella an… Continue reading

2017-09-21 Michael Zand NEWS
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Swedish company ZandCell to supply 160 million doses of COVID-19 vaccine to several countries around the world 2021-07-29
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Шведская компания ZandCell предложила России произвести 750 млн доз вакцин Sputnik V и Aurora 2021-07-29
Шведская компания ZandCell поставит 160 млн доз вакцины от COVID-19 в несколько стран мира 2021-07-22
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Swedish company ZandCell to supply 160 million doses of COVID-19 vaccine to several countries around the world 2021-07-29
Swedish company ZandCell has offered Russia 750 million dose vaccine capacity for Sputnik V and Aurora 2021-07-29
Шведская компания ZandCell предложила России произвести 750 млн доз вакцин Sputnik V и Aurora 2021-07-29
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MIT Technology Review

Even at $500K, Gene Therapy Could Be a Bargain for Some Diseases
MIT Technology Review
The U.S. Food and Drug Administration recently approved what it called the “first gene therapy” in the country. The therapy, called Kymriah and made by Novartis, uses a patient’s own cells—which are genetically modified outside the body—to treat a …
Novel Gene Therapy and Antisense Drugs to Offer Effective Cancer CureTMR Research Blog (press release) (blog)

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