CRISPR 2.0 Achieves Historic First: Complete Cure for Rare Genetic Disease in Human Trial
UC Berkeley scientists achieve the first complete cure for rare OTCD using…
CRISPR Breakthrough: Johns Hopkins Clinical Trial Cures Rare Genetic Disease in Adults for the First Time
Johns Hopkins' CRISPR clinical trial achieves first full cure for rare genetic…
CRISPR Breakthrough: First Human Trial Successfully Cures Rare Genetic Disease with No Side Effects
In a medical first, a Boston biotech firm cures Leber congenital amaurosis…
MIT’s CRISPR Breakthrough: First Human Cure for Rare Genetic Disease in Clinical Trials
MIT researchers achieve a historic first: using CRISPR to cure Leber congenital…
CRISPR Breakthrough: Gene Editing Cures Rare Blindness in Pioneering Human Trial
In a medical first, CRISPR gene editing has cured a rare form…
CRISPR Breakthrough: First Successful Gene Editing Cure for Rare Muscle Disorder in Phase 2 Human Trials
Boston's GenEdit Therapeutics announces the first CRISPR cure for rare muscle disorder…
Breakthrough CRISPR Therapy Achieves Full Reversal of Rare Muscle Disorder in Landmark Clinical Trial
In a medical milestone, CRISPR gene therapy has fully reversed symptoms of…
CRISPR Breakthrough: First Human Cure for Rare Muscle-Wasting Genetic Disease Achieved in Boston Biotech Trial
Boston biotech Vertex announces complete remission of Duchenne muscular dystrophy in first…
CRISPR Breakthrough: Gene Editing Cures Rare Genetic Disease in Historic First Human Trial
In a historic first, CRISPR gene editing has cured Leber congenital amaurosis…
Stanford’s CRISPR Breakthrough: First Successful Human Cure for Rare Muscular Dystrophy in Groundbreaking Trials
Stanford researchers have cured a rare muscular dystrophy using CRISPR in human…
