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Penn Medicine team wins $3M prize for FDA-approved gene therapy restoring inherited blindness.
A team from Penn Medicine and Children’s Hospital of Philadelphia won the Breakthrough Prize for developing the first FDA-approved gene therapy for an inherited blindness.
Their treatment, Luxturna, restores sight to patients who would otherwise be blind from childhood.
The work has inspired over 140 gene therapy trials for retinal diseases and comes with a $3 million award.
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El equipo de Penn Medicine gana el premio de 3 millones de dólares por la terapia génica aprobada por la FDA para restaurar la ceguera heredada.