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Duchenne Muscular Dystrophy-dmd
The U.S. FDA Grants Orphan Drug Designation to NS-089/NCNP-02 for the Treatment of DMD
2023-08-17
Entrada Hit With Clinical Hold on IND Application for Muscular Dystrophy Therapy
2022-12-20
Sarepta Submits BLA for First-Ever Duchenne Muscular Dystrophy Gene Therapy
2022-10-03
The FDA Granted These Three Companies Orphan Drug Designations in One Day
2022-05-13
Harnessing Viral Evolution to Deliver Gene Therapy to Specific Tissues
2021-09-13
Sarepta to Begin Phase 3 Rivalry with Pfizer after its DMD Gene Therapy Registers Encouraging Data
2021-05-21
Sarepta’s Stocks Drop 50% Following Middling Trial Data for Gene Therapy
2021-01-11
Eli Lilly Forays into Gene Editing with Precision BioSciences Collaboration
2020-11-21
The Future of CRISPR: Three Areas The Nobel Prize Winning Tech Will Be Most Impactful
2020-10-25
Australian Pharma Bags Government Funding to Fight Duchenne Muscular Dystrophy
2020-09-06
R&D
Altering the Treatment Landscape of Neurodegenerative Diseases Using Antisense Oligonucleotides (ASOs)
2020-08-17
Spotlight: New Gene Therapies on the Horizon for the Treatment of Neurogenetic Diseases
2020-08-03
Scientists Use CRISPR To Fight Duchenne Muscular Dystrophy
2020-01-29
December 31, 2015: Researchers First Used CRISPR to Treat a Genetic Disease in Mice
2017-12-31
LATEST
Revolutionary Technology Aims to Detect and Prevent Dementia and Mental Illness
2023-09-22
Connecting Global Biotech, Thailand’s Largest Biotech Event Takes Center Stage
2023-09-22
BIOHK2023: A place where biotechnology meets financial economics
2023-09-21
Connecting the Dots: TCELS Leads the Way for Thailand’s Life Sciences and Healthcare Innovations
2023-09-20
Deceptive Health Advice on TikTok Raises Concerns About Gynecologic Cancer Misinformation
2023-09-20
Dreams and Nightmares: the Mysterious Activities of the Brain During Deep Sleep
2023-09-20
GeneOnline’s Weekly News Highlights: Sept 11-Sept 15
2023-09-19
EVENT
2023-10-04
BioFuture 2023
New York city,USA
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