BridgeBio Pharma Announces New Acoramidis Data, 41% Reduction in Heart Failure Risk
BridgeBio Pharma (BBIO) announced new data from the Phase 3 ATTRibute-CM study at Heart Failure 2026, organized by the Heart Failure Association of the European Society of Cardiology, further demonstrating acoramidis' consistent and clinically meaningful benefit across the transthyretin amyloid cardiomyopathy disease spectrum, with new data demonstrating disease modifying effects across clinical outcomes, biomarkers, and functional capacity. Acoramidis is the only selective small molecule, orally administered, near-complete transthyretin stabilizer. In a late-breaking oral presentation shared by Senthil Selvaraj, M.D. of Duke University School of Medicine, U.S., acoramidis showed an association between the treatment-related increase in serum transthyretin and a significant reduction of sTTR variability over time, which is independently associated with reduced all-cause mortality. Findings included: Lower intraindividual sTTR variability and higher achieved sTTR levels were each independently associated with reduced risk of all-cause mortality. Participants with both higher achieved sTTR levels and less variable sTTR levels experienced the greatest survival benefit, while higher sTTR variability was associated with adverse clinical features of ATTR-CM. Acoramidis increased sTTR levels early and sustained them through Month 30, while significantly reducing sTTR variability versus placebo. Reduction in sTTR variability mediated 20% of acoramidis' treatment effect on mortality. Additionally, Bayer (BAYRY), BridgeBio's exclusive European licensing partner of acoramidis, presented a late-breaking oral presentation by Marianna Fontana, M.D. of University College London, UK, showing that acoramidis drove early and sustained reductions in the risk of outpatient worsening heart failure within 30 days. These findings included: Acoramidis reduced the risk of outpatient worsening heart failure versus placebo by 41%. Outpatient worsening heart failure was a strong predictor of mortality and cardiovascular hospitalizations, reinforcing its role as an early and clinically meaningful marker of disease progression. Even after adjusting for outpatient worsening heart failure, acoramidis reduced risk of mortality and recurrent cardiovascular hospitalizations by 41%. For the first time, BridgeBio also shared an anchored matching-adjusted indirect comparison presented by Emer Joyce, M.D., Ph.D. of the Mater Misericordiae University Hospital, IE, of acoramidis versus tafamidis using the pivotal study data with statistically significant, clinically meaningful benefit, which showed that: Acoramidis demonstrated a statistically significant, 34% reduction in cardiovascular hospitalizations versus tafamidis. Acoramidis showed a favorable mortality trend with 28% hazard reduction in all-cause mortality versus tafamidis, with consistent benefit across sensitivity analyses. Comparable safety profile observed between acoramidis and tafamidis. In addition to the presentations highlighted, three additional acoramidis posters were also shared at Heart Failure 2026, which included: Acoramidis Treatment Attenuates the Rise in NT-proBNP from Baseline to Month 30 Compared to Placebo Across all Subgroups, presented by Marianna Fontana, M.D., of University College London, UK. In ATTRibute-CM, acoramidis consistently blunted the 30-month increase in NT-proBNP by about 50% across all participant subgroups assessed, including advanced disease, compared with placebo, demonstrating its robust efficacy on a key biomarker of ATTR-CM disease progression. Consistent Benefit on Kansas City Cardiomyopathy Questionnaire Overall Summary Score with Acoramidis Treatment Compared with Placebo Across Participant Subgroups in ATTRibute-CM, presented by Dr. Fontana Acoramidis significantly attenuated the decline in heart failure-related health status compared with placebo in individuals with ATTR-CM. This effect was observed consistently across all pre-specified participant subgroups, including those with advanced heart failure symptoms. Effect of Acoramidis on Improvement or Maintenance of Heart Failure-Related Health Status as Assessed by KCCQ-OS Score in ATTRibute-CM, presented by Charles Sherrod, M.D. of Saint Luke's Health System, Kansas City, U.S.. In individuals with ATTR-CM, acoramidis treatment was associated with a significantly greater likelihood of maintenance or improvement in health status compared with placebo, suggesting a clinically relevant modification of disease trajectory. These data provide an integrated assessment of health status and survival to inform medical decision making.
Trade with 70% Backtested Accuracy
Analyst Views on BBIO
About BBIO
About the author

- Rising Cardiovascular Costs: The American Heart Association warns that U.S. heart disease costs are set to quadruple by 2050, with national healthcare spending nearing $5 trillion, compelling hospitals to rethink their diagnostic and treatment strategies for cardiac patients, thereby driving structural changes in the healthcare industry.
- Rapid Growth of AI Cardiology Market: The global AI cardiology market is projected to grow from $2.78 billion this year to over $14 billion by 2034, reflecting a strong demand for innovative technologies as health systems rush to deploy machine learning tools to address diagnostic backlogs.
- Showcasing VMS+™ 4.0 Technology: VentriPoint Diagnostics will showcase its AI-powered cardiac imaging platform at the AEPC conference in Italy, which converts standard 2D ultrasound scans into detailed 3D heart models, providing results comparable to cardiac MRI without the need for expensive machines and long wait times.
- International Collaborations and Market Expansion: VentriPoint has established partnerships for regulatory approval of VMS+™ 4.0 in China and is promoting cardiac diagnostics in Costa Rica and Indigenous communities in Canada, demonstrating its potential for global market expansion and commercial momentum.
- Cost Warning for Cardiovascular Disease: The American Heart Association warns that U.S. heart disease costs are set to quadruple by 2050, with national healthcare spending nearing $5 trillion, compelling hospitals to rethink their diagnostic and treatment approaches for cardiac patients, potentially leading to significant industry transformation.
- Growth of AI Cardiology Market: The global AI cardiology market is valued at $2.78 billion this year and is projected to exceed $14 billion by 2034, driving health systems to accelerate the deployment of machine learning tools to address diagnostic backlogs, thereby enhancing medical efficiency and patient satisfaction.
- Showcasing VMS+™ 4.0 Technology: VentriPoint Diagnostics will showcase its AI-powered cardiac imaging platform, VMS+™ 4.0, at the AEPC annual meeting in Italy, which can convert standard 2D ultrasound scans into detailed 3D heart models, providing results comparable to cardiac MRI while significantly reducing equipment costs and wait times.
- International Collaborations and Market Expansion: VentriPoint has established relationships with multiple international partners, including Lishman Global, which is applying for regulatory approval in China, and collaborations in Costa Rica and Indigenous communities in Canada, demonstrating its growth potential and strategic positioning in the global cardiac diagnostics market.
- Successful Clinical Trial: At the 2026 European Congress of Endocrinology, BridgeBio presented Phase 3 CALIBRATE trial results, showing that 76% of participants on encaleret achieved target serum and urine calcium levels at Week 24, a significant increase from 4% on conventional therapy, highlighting the drug's potential in treating ADH1.
- Market Opportunity: BridgeBio anticipates a U.S. launch of encaleret in early 2027, which, if approved, would be the first therapy specifically indicated for ADH1, addressing the urgent needs of nearly 2,000 diagnosed patients in the U.S. and indicating a substantial market opportunity.
- Favorable Safety Profile: No discontinuations were reported in the encaleret group, and the rate of serious adverse events was similar to the control group, indicating a good safety and tolerability profile that supports future market adoption.
- Future Research Plans: BridgeBio plans to initiate the RECLAIM-HP Phase 3 clinical study in Summer 2026, further exploring encaleret's applications in chronic hypoparathyroidism, thereby expanding its indications and enhancing the company's competitiveness in the genetic disease sector.
- Clinical Trial Results: BridgeBio Pharma's Phase 3 ATTRibute-CM study demonstrates Acoramidis' disease-modifying effects across clinical outcomes, biomarkers, and functional capacity, reinforcing its potential in treating transthyretin amyloid cardiomyopathy.
- FDA Approval Context: Acoramidis received FDA approval in November 2024 to reduce cardiovascular death and related hospitalizations, marking a significant milestone in the treatment of transthyretin-mediated amyloidosis.
- Biomarker Association: New data indicates a positive correlation between treatment-related serum transthyretin (sTTR) levels and early markers of disease progression, with higher sTTR levels and lower variability linked to improved survival outcomes.
- Reduced Heart Failure Risk: Patients treated with Acoramidis experienced a 41% reduction in heart failure risk, a 34% decrease in cardiovascular hospitalizations compared to placebo, and a 28% reduction in all-cause mortality, highlighting its significant clinical advantages.
- Significant Clinical Effects: Acoramidis demonstrated early and significant increases in serum transthyretin (sTTR) levels in the Phase 3 ATTRibute-CM study, reducing the risk of outpatient worsening heart failure by 41% within 30 days, showcasing its rapid impact in heart disease treatment.
- Mortality Reduction: The study revealed that Acoramidis significantly reduced sTTR variability (9.5% vs. 12.8%; p<0.001), which was associated with a decrease in all-cause mortality (HR: 0.56; p=0.014), indicating its potential in improving patient survival rates.
- Hospitalization Rate Decrease: Acoramidis achieved a statistically significant 34% reduction in cardiovascular hospitalizations compared to tafamidis (RRR: 0.66; 95% CI: 0.46–0.95), along with a favorable mortality trend, further solidifying its clinical value.
- Good Safety Profile: Acoramidis exhibited a comparable safety profile to tafamidis, with similar adverse event rates, ensuring its acceptability in clinical use and supporting its role as an effective treatment option for ATTR-CM.
- Attruby Sales Growth: BridgeBio Pharma reported $180.6 million in Attruby sales for Q1 2026, reflecting a 24% increase from the previous quarter, indicating strong market performance and positioning the company for continued revenue growth.
- Significant Clinical Data: CEO Neil Kumar highlighted that Attruby demonstrated a 49% reduction in cardiovascular mortality compared to tafamidis in clinical trials, enhancing the product's competitive edge and laying a solid foundation for future sales growth.
- Share Buyback Program: The Board authorized a $500 million share repurchase program aimed at leveraging current market undervaluation to enhance shareholder value while maintaining flexibility for future investments, which is expected to positively impact the stock price.
- Financial Outlook: CFO Thomas Trimarchi indicated that operational losses are expected to stabilize over the next two quarters, with a plan to achieve breakeven by 2027, reflecting the company's confidence in financial management and strategic planning for business expansion.










