New tumor cases show common gene therapy tool can come with risk
The FDA launches an investigation into Novartis' Zolgensma gene therapy following reports of new tumor cases.
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The FDA launches an investigation into Novartis' Zolgensma gene therapy following reports of new tumor cases.
Experimental brain gene therapy cuts drug-resistant epilepsy seizures by over ninety percent in human trials.
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Novartis reports cases of tumors in children following treatment with its spinal muscular atrophy gene therapy, Zolgensma.
An autonomous AI agent has performed a gene therapy brain injection on a live mouse after a refusal by an earlier model.
Recent coverage examines a fatal gene-editing trial in China that showed limited efficacy alongside severe safety concerns.
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Recent scientific coverage reveals that delivering the SRSF1 gene extends median lifespan and reverses aging indicators in aged mice.
Recent coverage highlights experimental optogenetic therapies and specialized goggles restoring partial vision in blind adults.
Swiss gene therapy for blindness, rooted in Nobel-winning research, shows further encouraging progress according to recent reports.
Recent scientific findings detail the use of optogenetic therapy and special goggles to restore limited vision in blind patients.
Gene therapy linked to Nobel-winning research shows promise in restoring limited sight to blind patients.
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FDA approves Ultragenyx's gene therapy Fayuvi for Sanfilippo syndrome at a price of $3.95 million.
Medical advancements in gene therapy are transforming the lives of sickle cell patients, highlighted by new treatments and cultural reflections.
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The FDA has placed a clinical hold on Regenxbio's gene therapy for Hunter Syndrome following safety concerns related to spine MRI findings.
Coverage reveals a third death in opaque Chinese clinical trials involving CAR-T therapy, intensifying global scrutiny.
The death of a child in a gene editing trial exposes the ethical perils and limits of scientific advancement.
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Personalized gene therapy using bespoke ASOs has enabled a teen with SCN2A-related epileptic encephalopathy to walk independently for the first time.
A $160 million non-profit initiative in Boston aims to revolutionize the development of genetic medicines for rare and ultra-rare diseases.
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Researchers have initiated the first human clinical trial focused on reversing cellular aging through experimental gene therapy.
The FDA is allowing Regenxbio to resubmit its gene therapy for Hunter syndrome, marking a reversal of a previous rejection.
A lupus treatment borrowed from cancer therapy is putting patients into remission—with one calling it life-changing.
The gene editing landscape is expanding rapidly through next-generation CRISPR tools and significant projected market growth through 2028.