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Late-stage study underway for BioMarin’s gene therapy for hemophilia A – Seeking Alpha

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2017-12-19 Michael Zand NEWS

HSS’ Dr. Christopher Mendias earns $800k grant for stem cell research — 5 notes – Becker’s Orthopedic & Spine

Late-stage study underway for BioMarin’s gene therapy for hemophilia A
Seeking Alpha
The first patient has been dosed in a Phase 3 clinical trial, GENEr8-1, assessing BioMarin Pharmaceutical’s (NASDAQ:BMRN) gene therapy valoctocogene roxaparvovec (VR) in patients with hemophilia A. The study is the first of two registration trials that …

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2017-12-19 Michael Zand NEWS

Mesothelioma Immunotherapy Clinical Trial Ends Abruptly – Asbestos.com

Asbestos.comMesothelioma Immunotherapy Clinical Trial Ends AbruptlyAsbestos.comA leading biopharmaceutical company has halted a once-promising mesothelioma clinical trial involving CRS-207 — a listeria-based cancer vaccine — citing efficacy and financi… Continue reading

2017-12-19 Michael Zand NEWS

New Gene Therapies Could Change Hemophilia Forever – Motley Fool

HSS’ Dr. Christopher Mendias earns $800k grant for stem cell research — 5 notes
Becker’s Orthopedic & Spine
The Orthopaedic Research and Education Foundation and National Stem Cell Foundation gave Christopher L. Mendias, PhD, of New York City-based Hospital for Special Surgery, a research grant. Here are five notes: 1. Dr. Mendias earned the OREF Clinical …

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2017-12-19 Michael Zand NEWS

TEDCO stem cell investments yield 1400 jobs in Maryland, report says – Baltimore Business Journal

Baltimore Business JournalTEDCO stem cell investments yield 1400 jobs in Maryland, report saysBaltimore Business JournalState-backed investments in stem cell research have resulted in the creation of nearly 1,400 new jobs over the past 10 years, accord… Continue reading

2017-12-19 Michael Zand NEWS

FDA Approves Gene Therapy for Rare Form of Blindness – U.S. News & World Report

New Gene Therapies Could Change Hemophilia Forever
Motley Fool
At last week’s American Society of Hemophilia conference, Spark Therapeutics (NASDAQ:ONCE) and BioMarin (NASDAQ:BMRN) presented promising data for gene therapy drugs that could change the way hemophilia is treated, making patients’ lives significantly …

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2017-12-19 Michael Zand NEWS

Juno, Celgene Report Impressive Results of CAR T-cell Therapy in B-cell Lymphoma – Lymphoma News Today

Lymphoma News TodayJuno, Celgene Report Impressive Results of CAR T-cell Therapy in B-cell LymphomaLymphoma News TodayThe CAR T-cell therapy JCAR017, developed by Juno Therapeutics and Celgene, eradicated B-cell lymphomas in more than two-thirds of pat… Continue reading

2017-12-19 Michael Zand NEWS

FDA Approves Novel Gene Therapy for Rare Form of Vision Loss – Medscape

MedscapeFDA Approves Novel Gene Therapy for Rare Form of Vision LossMedscapeFDA Approves Novel Gene Therapy for Rare Form of Vision Loss. Marcia Frellick. Disclosures. December 19, 2017. The US Food and Drug Administration (FDA) today approved a new ge… Continue reading

2017-12-19 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
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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FDA Approves Gene Therapy for Rare Form of Blindness
U.S. News & World Report
TUESDAY, Dec. 19, 2017 (HealthDay News) — A new gene therapy to treat children and adults with a rare type of inherited vision loss has been approved by the U.S. Food and Drug Administration. It’s the first gene therapy approved in the United States …