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BridgeBio's Acoramidis Demonstrates Sustained Cardiovascular Benefits in Phase 3 ATTR-CM Trial

24 days ago2 min read

Key Insights

  • BridgeBio Pharma presented detailed Phase 3 ATTRibute-CM study results showing acoramidis significantly reduced cardiovascular mortality and recurrent hospitalizations in ATTR-CM patients.

  • The treatment benefits were observed as early as the first month and sustained over 42 months of continuous therapy.

  • Acoramidis improved outcomes across both wild-type and variant ATTR-CM subgroups, supporting broad clinical adoption regardless of genetic subtype.

BridgeBio Pharma recently presented detailed Phase 3 results from the ATTRibute-CM study at the Heart Failure Society of America Annual Scientific Meeting, demonstrating that acoramidis (Attruby) significantly reduced cardiovascular mortality and recurrent hospitalizations in patients with transthyretin amyloid cardiomyopathy (ATTR-CM). The treatment benefits were observed as early as the first month and sustained over 42 months of continuous therapy.

Broad Efficacy Across Patient Subgroups

A key finding from the ATTRibute-CM study was that continuous acoramidis treatment improved outcomes across both wild-type and variant ATTR-CM subgroups. This broad efficacy profile supports the drug's potential for widespread clinical adoption regardless of genetic subtype, addressing a critical need in ATTR-CM treatment where patient populations can vary significantly in their underlying genetic characteristics.
The sustained benefit over 42 months represents a substantial duration of follow-up for a Phase 3 cardiovascular outcomes trial, providing clinicians with confidence in the drug's long-term efficacy profile. The early onset of benefits, detectable within the first month of treatment, suggests that patients may experience meaningful clinical improvements relatively quickly after initiating therapy.

Market Position and Commercial Outlook

The positive ATTRibute-CM data strengthens BridgeBio's case for Attruby's broad efficacy and may support continued prescription growth while reducing near-term adoption risks. The results underscore Attruby's impact on both wild-type and variant ATTR-CM patients, potentially solidifying the company's leading position in the market as competition intensifies from larger pharmaceutical companies.
BridgeBio Pharma is projected to reach $1.7 billion in revenue and $297.7 million in earnings by 2028, based on assumptions of annual revenue growth of 92.3% and a $1.07 billion increase in earnings from current losses of $776.4 million. However, the company's continued reliance on a single product for most of its revenue remains a key consideration for investors evaluating the company's long-term prospects.

Investment Implications

The ATTRibute-CM results represent one of BridgeBio's critical short-term catalysts for maintaining momentum in market uptake and clinical differentiation. The data's real-world relevance supports the investment thesis around ongoing clinical adoption and market expansion of Attruby for transthyretin amyloid cardiomyopathy.
Fair value estimates from the investment community range widely from $14.28 to $303.80 per share, reflecting the varied perspectives on the company's future potential. While the strong clinical results provide positive momentum, BridgeBio's heavy dependence on Attruby sales remains a central consideration for investors weighing the company's pipeline concentration and pressure to achieve sustainable profitability.
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