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BridgeBio Pharma Announces Submission of New Drug Application (NDA) to U S Food and Drug

- NDA submission is based on positive results from ATTRibute-CM Phase 3 study, including a highly statistically significant result, demonstrated by a Win Ratio of 1.8 (p<0.0001), on the primary

BridgeBio Pharma (BBIO) Announces Submission of NDA to FDA for Acoramidis for the Treatment of Patients with Transthyretin Amyloid Cardiomyopathy

BridgeBio Pharma (BBIO) Announces Submission of NDA to FDA for Acoramidis for the Treatment of Patients with Transthyretin Amyloid Cardiomyopathy
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BridgeBio Pharma Announces Submission of New Drug

BridgeBio Pharma Announces Submission of New Drug
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BridgeBio Pharma Presents Additional Clinical Outcomes Data from the Phase 3 ATTRibute-CM Study of Acoramidis in Patients with Transthyretin Amyloidosis Cardiomyopathy (ATTR-CM)

BridgeBio Pharma Presents Additional Clinical Outcomes Data from the Phase 3 ATTRibute-CM Study of Acoramidis in Patients with Transthyretin Amyloidosis Cardiomyopathy (ATTR-CM)

BridgeBio Pharma Presents Additional Clinical Outcomes Data from the Phase 3 ATTRibute-CM Study of Acoramidis in Patients with Transthyretin Amyloidosis Cardiomyopathy (ATTR-CM)
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