FDA Approves BridgeBio's Acoramidis Challenging Pfizer's Tafamidis with Potential of Alnylam's Amvuttra in ATTR-CM Market

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FDA Approves BridgeBio's Acoramidis Challenging Pfizer's Tafamidis with Potential of Alnylam's Amvuttra in ATTR-CM Market

BridgeBio has achieved a pivotal milestone with the FDA's approval of Attruby (acoramidis) for treating transthyretin amyloid cardiomyopathy (ATTR-CM). This approval is momentous given BridgeBio's previous setbacks, including a failed trial in 2021, and now positions Attruby against dominant market player Pfizer's tafamidis[2][3]. As a TTR stabilizer, Attruby has shown effectiveness in prolonging life and minimizing hospitalizations in clinical trials, which strengthens BridgeBio's competitive market standing[4][6]. This strategic market entry is further supported by strategic partnerships for distribution, such as with Bayer for Europe and AstraZeneca for Japan, setting the stage for a robust international market presence[2].