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  2. B. C. girl with leukemia seeks Christmas stem cell donor – DigitalJournal.com
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NEWS

Novartis-backed GenSight gets cash for gene therapy launch – FierceBiotech

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2017-06-23 Michael Zand NEWS

Novartis-backed GenSight gets cash for gene therapy launch – FierceBiotech


FierceBiotech

Novartis-backed GenSight gets cash for gene therapy launch
FierceBiotech
GenSight Biologics has raised (PDF) €22.5 million ($25.2 million) to prepare to bring gene therapy GS010 to market in the U.S. and Europe. The financing gives the Novartis-backed biotech enough cash to deliver data from two phase 3 trials next year and …
French Biotech Raises Over €22M to Launch a Gene Therapy to Restore SightLabiotech.eu (blog)

all 2 news articles »

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2017-06-23 Michael Zand NEWS

CRISPR crew’s lab test spotlights lead program in sickle cell disease, beta-thalassemia – Endpoints News


FierceBiotech

Novartis-backed GenSight gets cash for gene therapy launch
FierceBiotech
GenSight Biologics has raised (PDF) €22.5 million ($25.2 million) to prepare to bring gene therapy GS010 to market in the U.S. and Europe. The financing gives the Novartis-backed biotech enough cash to deliver data from two phase 3 trials next year and …
French Biotech Raises Over €22M to Launch a Gene Therapy to Restore SightLabiotech.eu (blog)

all 2 news articles »

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2017-06-23 Michael Zand NEWS

Sarepta Signs Gene Therapy R&D Deal for DMD – Drug Discovery & Development

CRISPR crew’s lab test spotlights lead program in sickle cell disease, beta-thalassemia
Endpoints News
CRISPR/Cas9 tech is still at a very early stage of development. But one of the top biotechs looking to make a breakthrough in the clinic got a chance today to explain why one of its preclinical studies helps demonstrate gene editing’s promise in …
European Hematology Association: Treating Sickle Cell Disease …PR Newswire (press release)

all 1 news articles »

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2017-06-23 Michael Zand NEWS

Immunotherapy Safely Treats Advanced Squamous Cell Carcinoma – Cancer Network

Sarepta Signs Gene Therapy R&D Deal for DMD
Drug Discovery & Development
Genethon specializes in a micro-dystrophin gene therapy approach that can target the majority of patients with DMD, according to the announcement. The organization has demonstrated proof-of-concept of their program through a robust gene expression in a …

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2017-06-23 Michael Zand NEWS

French Biotech Raises Over €22M to Launch a Gene Therapy to Restore Sight – Labiotech.eu (blog)

Immunotherapy Safely Treats Advanced Squamous Cell Carcinoma
Cancer Network
Immunotherapy Safely Treats Advanced Squamous Cell Carcinoma. News | June 23, 2017 | Skin Cancer (Nonmelanoma). By Mark L. Fuerst. A fully human anti–programmed death 1 (PD-1) monoclonal antibody is safe and effective for patients with …

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2017-06-23 Michael Zand NEWS

Firefly Gene Illuminates Ability of Optimized CRISPR-Cpf1 to Efficiently Edit Human Genome – Scicasts (press release) (blog)


Labiotech.eu (blog)

French Biotech Raises Over €22M to Launch a Gene Therapy to Restore Sight
Labiotech.eu (blog)
Gensight Biologics has announced a capital increase that totals €22.5M and will support the launch of its gene therapy for blindness in Europe and the US. Gensight has decided to give an additional financial push to its lead candidate, GS010, a gene …

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2017-06-23 Michael Zand NEWS

Stem cells: the future of medicine – Medical Xpress

Stem cells: the future of medicineMedical XpressWhile human embryos contain embryonic stem cells, which help them to develop, the use of those cells has been controversial. The scientists are using induced pluripotent stem cells instead, which are othe… Continue reading

2017-06-23 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
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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Scicasts (press release) (blog)

Firefly Gene Illuminates Ability of Optimized CRISPR–Cpf1 to Efficiently Edit Human Genome
Scicasts (press release) (blog)
Professor Michael Farzan, co-chair of TSRI’s Department of Immunology and Microbiology, and TSRI Research Associate Guocai Zhong improved the efficiency of the CRISPR–Cpf1 gene editing system by incorporating guide RNAs with “multiplexing” …