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Intellia Therapeutics' CRISPR therapy shows promising results in treating ATTR amyloidosis.
Intellia Therapeutics reported positive results from a Phase 1 trial of nexiguran ziclumeran, a CRISPR-based gene therapy for ATTR amyloidosis.
The treatment showed rapid and lasting reductions in disease markers and improvements in patient conditions after a single dose.
The therapy was found to be safe and well-tolerated, with benefits observed in both heart and nerve-related symptoms of the disease.
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La terapia CRISPR de Intellia Therapeutics muestra resultados prometedores en el tratamiento de la amiloidosis ATTR.