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Pharmaceutical biotechnology recently achieved its most ambitious goal: gene therapy. Instead of administering a protein, biotech now delivers the gene that codes for that protein. Using viral vectors (engineered, harmless viruses), drugs like Luxturna (for inherited blindness) and Zolgensma (for spinal muscular atrophy) correct the underlying genetic defect. While these drugs cost upwards of $2 million per patient, they offer a potential one-time cure, dramatically reducing lifetime healthcare costs.

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