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BridgeBio to Present New Acoramidis Data, Including Independent Comparative Real-World EHR Data at the HFSA Annual Scientific Meeting 2026

Key Takeaway: BridgeBio Pharma will present new data on acoramidis at the HFSA Annual Scientific Meeting 2026. The presentations will include one oral presentation, three rapid-fire oral presentations, and six poster presentations focused on the treatment of transthyretin amyloid cardiomyopathy (ATTR-CM). Acoramidis is highlighted as a first-line treatment option, with data supporting its clinical profile and effectiveness.

Market Sentiment Analysis

POSITIVE FACTORS

  • Acoramidis is presented as a first-line treatment for ATTR-CM.
  • Data reinforces the differentiated clinical profile of acoramidis.
  • The company showcases multiple presentations at a significant scientific meeting.

CONCERNS & RISKS

  • Adverse reactions such as diarrhea and abdominal pain were reported.
  • The article mentions the challenges of drug development for small patient populations.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Best trade, last catalyst
+41%
120-day peak, hindsight
Typical move
4.2%
average across 13 past catalysts
Cash runway
~29 mo
Minimal dilution risk
Lead asset
BBP-418
Phase 2 · LGMD2I

Full Press Release Details

PALO ALTO, Calif., Oct. 06, 2026 (GLOBE NEWSWIRE) -- BridgeBio Pharma, Inc. (Nasdaq: BBIO) ("BridgeBio" or the "Company"), a commercial-stage, multi-product biopharmaceutical company focused on developing medicines for genetic conditions, announced today that one oral presentation, three rapid-fire oral presentations, and six poster presentations on acoramidis in individuals with transthyretin amyloid cardiomyopathy (ATTR-CM) will be shared at the Heart Failure Society of America (HFSA) Annual Scientific Meeting (ASM) 2026, taking place in Phoenix, Arizona on October 9-12, 2026. The data further strengthen the differentiated clinical profile of acoramidis, reinforcing it as the first-line treatment of choice for individuals with ATTR-CM. Acoramidis is the only selective small molecule, orally administered, near-complete (≥90%) transthyretin (TTR) stabilizer.
Acoramidis is approved as Attruby ® by the U.S. FDA and is approved as BEYONTTRA ® by the European Medicines Agency (EMA), Japanese Pharmaceuticals and Medical Devices Agency, Swissmedic, the Swiss Agency for Therapeutic Products, the UK Medicines and Healthcare Products Regulatory Agency, and the Brazilian Health Regulatory Agency (ANVISA) with all labels specifying near-complete stabilization of TTR.
Oral Presentation: Association Between the Burden of Cardiovascular-Related Hospitalizations and All-Cause Mortality in Transthyretin Amyloid Cardiomyopathy: Insights from ATTRibute-CM Presenter: Quan Bui, M.D., UC San Diego Health, U.S. Date/time: Saturday, October 10 at 7:45 am MST
Rapid-Fire Oral Presentations: Real-World Comparative Effectiveness Study of Acoramidis Versus Tafamidis in Transthyretin Amyloid Cardiomyopathy Using the Epic COSMOS Data Platform Presenter: David Lanfear, M.D., M.S., Chief Scientific Officer of Henry Ford Health, U.S. Date/time: Sunday, October 11 at 11:30 am MST
Early eGFR Dip Following Acoramidis Initiation is Associated with Reduced Risk of Mortality and Recurrent Cardiovascular-Related Hospitalizations in ATTR-CM Presenter: Ahmad Masri, M.D., M.S., Oregon Health & Science University, U.S. Date/time: Sunday, October 11 at 11:12 am MST
Ratio of Serum Transthyretin to NT-proBNP is a Novel Prognostic Measure for Transthyretin Amyloid Cardiomyopathy: Insights from ATTRibute-CM Presenter: James L. Januzzi, M.D., Massachusetts General Hospital, U.S. Date/time: Sunday, October 11 at 10:45 am MST
Poster Presentations: Falls and Fractures Drive Increased Hospitalizations and Costs in Patients with Transthyretin Amyloid Cardiomyopathy Compared with Controls Presenter: Nitasha Sarswat, M.D., University of Chicago, U.S. Date/time: Friday, October 9 at 6:15 pm MST
Evaluating the Long-Term Effects of Acoramidis on Cardiac Function, Structure, and Amyloid Burden in Transthyretin Amyloid Cardiomyopathy: ASCEND-ATTR Presenter: Ahmad Masri, M.D., M.S., Oregon Health & Science University, U.S. Date/time: Saturday, October 10 at 1:45 pm MST
Real-World Burden of Transthyretin Amyloid Cardiomyopathy Disease and Outcomes in Patients on Tafamidis Prior to Initiating Acoramidis Presenter: Richard Wright, M.D., Pacific Heart Institute, U.S. Date/time: Saturday, October 10 at 5:45 pm MST
Acoramidis Reduces Risk of Cardiovascular-Related Mortality and Hospitalization in Women with Transthyretin Amyloid Cardiomyopathy Presenter: Margot Davis, M.D., University of British Columbia, CA Date/time: Saturday, October 10 at 6:15 pm MST
Acoramidis Preserves Functional Capacity and Quality of Life in p.Val142Ile Variant Transthyretin Amyloid Cardiomyopathy: Results from ATTRibute-CM Presenter: Lily Stern, M.D., Cedars-Sinai Heart Institute, U.S. Date/time: Sunday, October 11 at 8:15 am MST
Effect of Acoramidis on Heart Failure-Related Health Status Before and After Cardiovascular-Related Hospitalization: Insights from ATTRibute-CM Presenter: Ahmad Masri, M.D., M.S., Oregon Health & Science University, U.S. Date/time: Sunday, October 11 at 8:15 am MST

About Attruby ® (acoramidis)

INDICATION Attruby is a transthyretin stabilizer indicated for the treatment of the cardiomyopathy of wild-type or variant transthyretin-mediated amyloidosis (ATTR-CM) in adults to reduce cardiovascular death and cardiovascular-related hospitalization.
IMPORTANT SAFETY INFORMATION Adverse Reactions Diarrhea (11.6% vs 7.6%) and upper abdominal pain (5.5% vs 1.4%) were reported in patients treated with Attruby versus placebo, respectively. The majority of these adverse reactions were mild and resolved without drug discontinuation. Discontinuation rates due to adverse events were similar between patients treated with Attruby versus placebo (9.3% and 8.5%, respectively).
About BridgeBio BridgeBio exists to develop transformative medicines for genetic conditions. Millions of people worldwide living with genetic conditions lack treatment options, often because drug development for small patient populations can be commercially challenging. We aim to bridge the gap between advancements in genetic science and meaningful medicines for underserved patient populations. Our decentralized, hub-and-spoke model is designed for speed, precision, and scalability. Autonomous and empowered teams focus on individual conditions, while a central hub provides the clinical, regulatory, and commercial capabilities needed to bring innovation to market. For more information, visit bridgebio.com and follow us on LinkedIn, X, Facebook, Instagram, YouTube and TikTok.

BridgeBio Media Contact: Kaitlyn Reilly, Director, Communications contact@bridgebio.com (650) 789-8220

BridgeBio Investor Contact: Kristen Kelleher, Director, Investor Relations ir@bridgebio.com

Frequently Asked Questions

What is acoramidis used for?

Acoramidis is used to treat transthyretin amyloid cardiomyopathy (ATTR-CM) in adults.

When will the HFSA Annual Scientific Meeting 2026 take place?

The HFSA Annual Scientific Meeting 2026 will be held from October 9-12, 2026.

What presentations will BridgeBio share at the HFSA meeting?

BridgeBio will present one oral presentation, three rapid-fire presentations, and six posters on acoramidis.

What are the common adverse reactions to acoramidis?

Common adverse reactions include diarrhea and upper abdominal pain.

Last updated: Oct 6, 2026