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New gene therapy for metachromatic leukodystrophy proves effective in mice

New gene therapy for metachromatic leukodystrophy proves effective in mice
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Paris , France-general- , France , Emilie-audouard , Methods-clinical-development , Paris-brain-institute , Molecular-therapy , Clinical-development ,

Reducing The Number Of Clinical Holds On Cell And Gene Therapies Approaches For Sponsors And The FDA

Reducing The Number Of Clinical Holds On Cell And Gene Therapies Approaches For Sponsors And The FDA
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Liz-essley-whyte , Brenda-sandburg , Sandy-kweder , Sean-hilscher , Peter-marks , Sandra-kweder , Gene-therapies-advisory-committee , Office-of-therapeutic-products , Eliquent-life-sciences-greenleaf-health , Georgetown-university , Beam-therapeutics-inc , Methods-clinical-development

The Future of Food Allergy Management

Food allergies, triggered by specific allergens, can lead to severe reactions like anaphylaxis. However, innovative treatments such as immunotherapy are revolutionizing allergy management.

Therapiae-experimentalis , Evan-lorne-shutterstock , Omalizumab-xolair , Us-food-and-drug-administration , Methods-clinical-development , Allergy-amulet , Machine-learning , Deep-learning , Image-credit , Pollen-forecast , Emerging-therapies

Data on Delandistrogene Moxeparvovec Can Inform Future Gene Therapies

The FDA approved delandistrogene moxeparvovec-rokl (Elevidys, Sarepta Therapeutics) in June to treat Duchenne muscular dystrophy in ambulatory pediatric patients aged 4 through 5 who have a confirmed DMD gene mutation.


Methods-clinical-development , National-organization-for-rare-disorders , Sarepta-therapeutics , Molecular-therapy , Image-credit , Ther-methods-clin , Updated-june , Updated-august , Delandistrogene-moxeparvovec- , Elevidys , Dmd-gene-mutation

Cellectis Reports Financial Results for Third Quarter and First Nine Months 2023

•  Strategic Collaboration and Investment Agreements signed with AstraZenecaUpdated results of the Phase I BALLI-01 Trial evaluating UCART22 in r/...

France , United-states , New-york , Paris , France-general- , Raleigh , North-carolina , French , Arthur-stril , Les-laboratoires-servier , Patricia-sosa-navarro , Ashleyr-robinson

First ever gene therapy trial for children with Hunter syndrome opens

First ever gene therapy trial for children with Hunter syndrome opens
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Manchester , United-kingdom , Bob-stevens , Rob-wynn , Stuart-ellison , Simon-jones , Health-research-authority , University-of-manchester , Manchester-university , Healthcare-products-regulatory-agency , Foundation-trust , Methods-clinical-development

Fortress Biotech (FBIO) Announces Option Agreement with City of Hope for Exclusive Worldwide Rights to use a Novel Bispecific CMV/HIV CAR T Cell Therapy

Fortress Biotech (FBIO) Announces Option Agreement with City of Hope for Exclusive Worldwide Rights to use a Novel Bispecific CMV/HIV CAR T Cell Therapy
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Cellectis and Imagine Institute Publish A Proof-Of-Concept Study of a Gene Surgery Candidate to Treat Activated Phosphoinositide 3-Kinase ? Syndrome Type 1 (APDS1)

Cellectis and Imagine Institute Publish A Proof-Of-Concept Study of a Gene Surgery Candidate to Treat Activated Phosphoinositide 3-Kinase ? Syndrome Type 1 (APDS1)
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Cellectis and Imagine Institute Publish A Proof-Of-Concept Study of a Gene Surgery Candidate to ...

NEW YORK, Oct. 12, 2023 (GLOBE NEWSWIRE) -- Cellectis (the “Company”) (Euronext Growth: ALCLS - NASDAQ: CLLS), a clinical-stage biotechnology company using its pioneering gene-editing platform to develop life-saving cell

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