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Duchenne muscular dystrophy, Regenxbio and gene therapy
Regenxbio says gene therapy strengthened boys with Duchenne muscular dystrophy
Based on a small trial with positive muscle performance data, Regenxbio is expected to pursue approval of its gene therapy for Duchenne muscular dystrophy.
Muscular dystrophy gene therapy uses cells to stitch together mRNA strands in mice
Gene therapy for some diseases, including Duchenne muscular dystrophy (DMD), can be tricky because the needed gene is often too large to fit inside the viral vector used for delivery. | Gene therapy for some diseases,
Regenxbio Share Surge 20% on Duchenne Muscular Dystrophy Treatment Trial Data, Expansion
Regenxbio shares surged 20% after disclosing new, positive efficacy and safety data of its Duchenne muscular dystrophy treatment. Shares were recently trading around $11.55. The stock is down 46% on the year.
Regenxbio eyes 2026 filing for Duchenne muscular dystrophy gene therapy
Regenxbio has revealed plans to submit a biologics licence application (BLA) for RGX-202, its investigational gene therapy for Duchenne muscular dystrophy (DMD), following positive data from the Phase I/II portion of its AFINITY DUCHENNE trial.
2h
Parent Project Muscular Dystrophy Culminates 30th Anniversary with Celebratory "Investing in Every Future" Event
Parent Project Muscular Dystrophy (PPMD), a nonprofit organization leading the fight to end Duchenne, commemorated its 30th ...
BioSpace
1d
Regenxbio Gears Up to Challenge Sarepta in DMD as Gene Therapy Advances to Pivotal Studies
Regenxbio is pushing its Duchenne muscular dystrophy gene therapy into pivotal development, with a BLA planned for ...
rheumatologyadvisor
1h
FDA Roundup: Rheumatology Drug Alerts
Throughout 2024, the FDA issued new drug approvals and expanded treatment indications across various rheumatologic diseases.
3h
Capricor Therapeutics Granted Orphan Drug and ATMP Status for Deramiocel by European Medicines Agency
Milestone represents a significant step forward in the development of deramiocel for the treatment of Duchenne muscular ...
FierceBiotech
1d
After seeing improved muscle function in phase 1/2 trial, Regenxbio launches pivotal DMD study
Regenxbio’s investigational gene therapy improved muscle function for patients with Duchenne muscular dystrophy (DMD) in a phase 1/2 study. | Regenxbio’s investigational gene therapy improved muscle ...
Business Insider
2d
Regenxbio initiates pivotal phase of Affinity Duchenne trial of RGX-202
a potential best-in-class gene therapy for
Duchenne
muscular
dystrophy
, has advanced to pivotal stage and dosed its first patient. The company also announced new, positive efficacy and safety ...
12d
Sarepta stops work on clinical-stage Duchenne treatment
After winning an expanded approval for its gene therapy to treat Duchenne muscular dystrophy earlier this year, Sarepta ...
4d
on MSN
I Just Watched The Remarkable Life of Ibelin, And I Was So Moved By How Role-Playing Games Can Empower People with Disabilities
It’s easy for those who play or watch the best movies based on video games to want to be immersed in that fictional world.
1d
Promising Initial Data and Favorable Regulatory Pathway Support Buy Rating for RegenXBio’s RGX-202 in DMD Treatment
Analyst Gena Wang from Barclays maintained a Buy rating on RegenXBio (RGNX – Research Report) and keeping the price target at $50.00.Don't Miss ...
Muscular Dystrophy News
2h
How I experienced inclusion (and didn’t) during my education
Columnist Shalom Lim tells an international conference about his experiences with inclusion during his education in Singapore ...
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Related topics
Regenxbio
Food and Drug Administration
RGX-202
Phases of clinical research
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