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Adagio Medical’s ULTA Technology to Be Featured at the Heart Rhythm 2026 Conference

Key Takeaway: Adagio Medical Holdings, Inc. will showcase its Ultra-low Temperature Ablation (ULTA) technologies at the Heart Rhythm 2026 conference in Chicago. The presentations will highlight the use of ULTA for treating scar-related ventricular tachycardia. The company is also conducting the FULCRUM-VT trial, which is pivotal for seeking FDA approval for its vCLAS™ Cryoablation System.

Market Sentiment Analysis

POSITIVE FACTORS

  • Adagio's ULTA technology will be prominently featured at a major conference.
  • The technology is designed for effective treatment of ventricular tachycardia.
  • The company is advancing its clinical trials, which may lead to FDA approval.

Full Press Release Details

Use of ULTA Across Broad Spectrum of Ventricular Tachycardias to be Highlighted in Multiple Scientific Presentations, Including Late-Breaking Clinical Trial Session
LAGUNA HILLS, Calif.--(BUSINESS WIRE)--Adagio Medical Holdings, Inc. (Nasdaq: ADGM) (“Adagio” or “the Company”), a leading innovator in catheter ablation technologies for the treatment of cardiac arrhythmias, today announced that its Ultra-low Temperature Ablation technologies (ULTA) for the treatment of scar-related ventricular tachycardia will be featured in several presentations at the Heart Rhythm Society's 47th Annual Scientific Sessions – Heart Rhythm 2026 conference, to be held from Thursday, April 23 to Sunday, April 26, 2026, in Chicago, Illinois at the McCormick Place Convention Center.
In addition to its booth and technology suite, Adagio’s ULTA technologies will be featured in several events and presentations:
Friday, April 24, 2026
Saturday, April 25, 2026
Sunday, April 26, 2026: Late-Breaking Clinical Trial Presentation
About Adagio Medical Holdings, Inc.
Adagio is a medical device company focused on developing and commercializing products for the treatment of cardiac arrhythmias utilizing its novel, proprietary, catheter-based Ultra-Low Temperature Ablation (ULTA, formerly known as ULTC) technology. ULTA is designed to create large, durable lesions extending through the depth of both diseased and healthy cardiac tissue, all through an endocardial approach. The Company is currently focused on the treatment of ventricular arrhythmias with its purpose-built vCLAS™ Cryoablation System, which is CE Marked and is currently under evaluation in the Company’s FULCRUM-VT U.S. Pivotal IDE Trial.
About FULCRUM VT
FULCRUM-VT (Feasibility of Ultra-Low Temperature Cryoablation in Recurring Monomorphic Ventricular Tachycardia) is a prospective, multi-center, open-label, single-arm trial, which has fully enrolled 209 patients with structural heart disease of both ischemic and non-ischemic cardiomyopathy, indicated for catheter ablation of drug refractory VT in accordance with current treatment guidelines. The results of the study will be used to apply for U.S. Food and Drug Administration (FDA) premarket approval (PMA) for Adagio’s vCLAS™ Cryoablation System, potentially leading to the broadest industry indication for purely endocardial ablation of scar-mediated VT.
Adagio’s vCLAS™ Cryoablation System is commercially available for the treatment of monomorphic VT in Europe and select other geographies but is limited to investigational use in the United States.
Debbie KasterChief Financial Officer and Chief Business Officerdkaster@adagiomedical.com

Frequently Asked Questions

What is the ULTA technology by Adagio Medical?

Adagio's ULTA technology is designed for catheter ablation of cardiac arrhythmias, specifically targeting scar-related ventricular tachycardia.

When is the Heart Rhythm 2026 conference?

The Heart Rhythm 2026 conference will take place from April 23 to April 26, 2026, in Chicago, Illinois.

What is the FULCRUM-VT trial?

The FULCRUM-VT trial evaluates the feasibility of ULTA in treating recurring monomorphic ventricular tachycardia and has fully enrolled 209 patients.

Is the vCLAS Cryoablation System available in the US?

Currently, the vCLAS Cryoablation System is limited to investigational use in the U.S. but is commercially available in Europe.

Last updated: Apr 17, 2026