HeartBeam Reports Second Quarter 2024 Results

In This Article:

Continued Clinical and Regulatory Progress on the HeartBeam AIMIGo? System

Enrollment Complete in VALID-ECG Clinical Study That Will Be the Basis of the Upcoming FDA Submission on the 12-Lead Synthesis Software

Management to Host Webcast and Conference Call Today at 4:30 p.m. ET

SANTA CLARA, Calif., August 14, 2024--(BUSINESS WIRE)--HeartBeam, Inc. (NASDAQ: BEAT), a medical technology company focused on transforming cardiac care through the power of personalized insights, has reported its financial and operational results for the second quarter ended June 30, 2024.

Second Quarter & Subsequent 2024 Operational Highlights

The Company made steady progress toward key clinical and regulatory milestones on its HeartBeam AIMIGo? System.

AIMIGo 510(k) Submission:

  • The 510(k) submission for the HeartBeam AIMIGo System is currently being reviewed by the FDA.

  • AIMIGo is a credit card-sized, cable-free cardiac monitoring device that will be capable of producing a 12-lead ECG by leveraging the Company’s core vector technology, which captures 360-degree signals of the heart’s electrical activity. The Company owns patents supporting the underlying technology.

  • This is the cornerstone submission for HeartBeam and will be the basis of future submissions.

  • The Company has successfully resolved the vast majority of the questions the FDA has asked. During the second quarter of 2024 the FDA requested additional information, which the Company is in the process of providing. The Company is working with the FDA to address the small number of remaining questions.

  • The Company continues to plan for a limited launch of AIMIGo by the end of 2024.

12-Lead Synthesis Software Submission:

  • HeartBeam has completed two pre-submission meetings with the FDA on the planned second 510(k) submission, which will be submitted after the initial clearance of the AIMIGo System.

  • The second submission is focused on the algorithms that convert the 360-degree signals captured by the AIMIGo System into a synthesized 12-lead ECG.

  • A key component of the submission will be the results of the VALID-ECG pivotal study, which is designed to demonstrate the similarity between the synthesized 12-lead ECG and a standard 12-lead ECG.

  • Patient enrollment for VALID-ECG was completed on June 20, 2024.

  • The Company currently anticipates submitting the 510(k) application soon after receiving clearance for the AIMIGo System.

Other Highlights:

  • New data presented at the European Heart Rhythm Association (EHRA) conference in April marked the first scientific presentation on HeartBeam AI, the Company’s deep learning technology. The data validated that applying HeartBeam AI to vectorcardiography (VECG) delivered distinctly improved performance in the detection of atrial flutter over single-lead ECGs. Atrial flutter is a common arrhythmia that significantly increases a patient’s risk for stroke.

  • Additionally, new data presented at the Heart Rhythm Society (HRS) Conference in May demonstrated that combining HeartBeam AI with VECG outperformed an expert panel of electrophysiologists in detecting atrial flutter when reviewing 12-lead ECGs. Data showed that applying AI to VECG data provides more consistent and reliable detection of atrial flutter.

  • HeartBeam AIMIGo was selected as winner of the "Best New ECG Technology Solution" award in the 8th annual MedTech Breakthrough Awards program.

  • HeartBeam was added to the Russell Microcap? Index effective after the market close on June 28, 2024.

  • Cash and cash equivalents totaled approximately $9.2 million as of June 30, 2024, enabling the Company to execute on upcoming clinical and regulatory milestones.