Tag Archives: The Stem Cell Blog

UChicago Medicine Working to Offer Breakthrough CAR T-Cell Gene Therapy Approved Today by FDA – Newswise (press release)

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2017-08-30 NEWS

UChicago Medicine Working to Offer Breakthrough CAR T-Cell Gene Therapy Approved Today by FDA
Newswise (press release)
CAR T-cell therapy has revolutionized the treatment of acute lymphoblastic leukemia,” according to cancer specialist John Cunningham, MD, chair of pediatrics at the University of Chicago and physician-in-chief at Comer Children’s Hospital. “I came to

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2017-08-30 NEWS

The Scientist

First CAR T-Cell Therapy Approved in US
The Scientist
ALLINONEMOVIE, PIXABAYThe US Food and Drug Administration (FDA) announced today (August 30) that it has approved the first therapy involving chimeric antigen receptor (CAR) T cells for clinical use. Each dose of Novartis’s drug, Kymriah, will consist

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2017-08-30 NEWS

UChicago Medicine working to offer breakthrough CAR T-cell gene therapy approved by FDA
EurekAlert (press release)
CAR T-cell therapy has revolutionized the treatment of acute lymphoblastic leukemia,” according to cancer specialist John Cunningham, MD, chair of pediatrics at the University of Chicago and physician-in-chief at Comer Children’s Hospital. “I came to

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2017-08-30 NEWS

US clears first ‘living drug’ for tough childhood leukemia
ModernHealthcare.com
The CART cell treatment developed by Novartis Pharmaceuticals and the University of Pennsylvania is the first type of gene therapy to hit the U.S. market — and one in a powerful but expensive wave of custom-made “living drugs” being tested against

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2017-08-30 NEWS

Medical Xpress

Blunting CRISPR’s ‘scissors’ gives new insight into autoimmune …
Science Daily
A research team has used a modified version of the gene-editing technique CRISPR to find enhancers — not by editing them but by prompting them into action.
CRISPRa Method Identifies Gene Enhancers Affecting T Cell …GenomeWeb

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2017-08-30 NEWS

US clears first ‘living drug’ for tough childhood leukemia
Orlando Sentinel
The CART cell treatment developed by Novartis Pharmaceuticals and the University of Pennsylvania is the first type of gene therapy to hit the U.S. market — and one in a powerful but expensive wave of custom-made “living drugs” being tested against