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ستاد فرهنگسازی اقتصاد دانش بنیان Novartis announces first CAR-T cell therapy BLA for pediatric and young adult patients with r/r B-cell ALL granted FDA Priority Review

Novartis announces first CAR-T cell therapy BLA for pediatric and young adult patients with r/r B-cell ALL granted FDA Priority Review

Novartis announced today that the US Food and Drug Administration (FDA) has accepted the companys Biologics License Application (BLA) filing and granted priority review for CTL019, an investigational chimeric antigen receptor T cell (CAR-T) therapy, in relapsed and refractory (r/r) pediatric and young adult patients with B-cell acute lymphoblastic leukemia (ALL). This is the first BLA submission by Novartis for a CAR-T. The priority review designation is expected to shorten the anticipated review time by the FDA.

ستاد فرهنگسازی اقتصاد دانش بنیان Sickle Cell Anemia Patient Cured by Gene Therapy

Sickle Cell Anemia Patient Cured by Gene Therapy

In a world first, a teenager with sickle cell disease achieved complete remission after an experimental gene therapy at Necker Childrens Hospital in Paris, researchers say.

ستاد فرهنگسازی اقتصاد دانش بنیان Stem cell therapy has turned out to be a ray of hope for most patients who are trying to find a cure for incurable diseases.
Stem cell treatment could be a proven therapy for diabetes, autism

Stem cell therapy has turned out to be a ray of hope for most patients who are trying to find a cure for incurable diseases.

Stem cell therapy has turned out to be a ray of hope for most patients who are trying to find a cure for incurable diseases. Researchers and experts believe India has been at the top in the development of stem cell treatment followed by several other countries like China and Japan. However, due to lack of awareness, most people dont think of stem cell therapy as an option for treating most of the incurable diseases.

ستاد فرهنگسازی اقتصاد دانش بنیان The breakthrough gene-editing technology is moving forward

The breakthrough gene-editing technology is moving forward

According to Time.com website, An advisory panel at the National Institutes of Health (NIH) has approved a proposal to use the gene-editing technology CRISPR on human cells. It’s the first trial involving humans to be approved in the U.S.

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