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The FDA approval significantly enhances BBIO's product portfolio and market potential, similar to other successful drug launches.
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FDA approved BBIO's Attruby for ATTR-CM treatment, boosting BBIO's market position. Attruby shows near-complete TTR stabilization, significantly reducing cardiovascular mortality. Phase 3 study enrolled 632 patients, demonstrating improved cardiovascular outcomes. Bayer AG granted exclusive rights for European commercialization of Attruby. Attruby's approval enhances BBIO's competitive edge against Pfizer's tafamidis.
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