An innovative method of gene therapy to treat hearing and balance disabilities caused by impaired function of the inner ear ...

Some of the most expensive drugs currently in use are gene therapies to treat specific diseases, and their high cost limits ...

Beyond its scientific program, the Cellex Symposium 2025 provided a forum for interdisciplinary exchange and collaboration. Researchers, clinicians, and industry representatives discussed ways to ...

In a first for adults in Singapore, scientists are conducting gene editing trials on heart patients to correct defects at ...

As a new €2 million gene therapy research project funded by APC Microbiome Ireland and Research Ireland is announced, we speak with the project lead Prof Niall Barron about its potential and how ...

The FDA is said to be making a U-turn on uniQure’s one-time gene therapy candidate for Huntington’s disease despite the ...

A single infusion of CRISPR Therapeutics' experimental gene therapy was safe and reduced levels of harmful LDL cholesterol ...

Opus Genetics has completed a Type B Regenerative Medicine Advanced Therapy (RMAT) meeting with the US Food and Drug Administration (FDA) regarding OPGx-LCA5, its gene therapy candidate for Leber ...

We have written about the promise of gene therapy to correct genetic disease many times. An exciting development happened ...

Emerging biotechnologies, strategic collaborations, and growing focus on personalized and regenerative medicine are accelerating the next wave of gene therapy innovation.Austin, Nov. 05, 2025 (GLOBE ...

New Product Shortage PLUS Endorsement fills a critical coverage gap for injury-related claims arising from product ...