In contrast, the HeartBeam AIMIGo is an easy-to-use, very concise system that synthesizes a 12-lead ECG. The key aim of the HeartBeam technology is to quickly and accurately help clinicians identify the full range of cardiac conditions, including a heart attack, outside of a medical institution. The AIMIGo device, coupled with a smartphone app and cloud-based diagnostic software, facilitates remote evaluation of cardiac symptoms by physicians and we believe it could reduce the critical time to intervention for heart attack patients. Shortening that time from symptoms to the door of a medical facility would reduce complications and save many lives. An effective triage tool in the hands of patients could also reduce the number of unnecessary emergency room visits and reduce costs to the healthcare.

So why do we think that an easy-to-use 12-lead ECG with patients is transformational? First, having the ability for patients to take frequent 12-lead readings over time and in a variety of real-life settings potentially has huge diagnostic value. Whenever a patient is feeling symptoms, they can get a 12-lead reading that will be reviewed by a physician. Secondly, trending a 12-lead ECG, both symptomatic and asymptomatic over time, will allow the physicians to gain insight to help guide cardiac care. Frequent 12-lead ECGs to create a trending and insightful way of tracking a cardiac condition. Finally, combining deep learning algorithms with a large number of student-only collected ECGs has the potential to create an unsurpassed predictive and diagnostic algorithm.

We have the opportunity to address not only the atrial fibrillation markets, but also the coronary artery disease market, which is 6 times larger. In the United States, there are approximately 3 million AFib patients, representing a $2 billion market. There are approximately 20 million coronary artery disease patients, which is a $12 billion market. So, the overall opportunity in the U.S. only is about $14 billion. I’d like to now turn the call over to our President, Rob Eno.

Rob Eno: Thanks, Branislav. We wanted to give an update on our progress related to AIMIGo. Our initial clearance for the AIMIGo system will be a major milestone for the company and it’s important for many reasons. To start, we expect this to be the first patient-held 3D VECG device to be cleared by the FDA. Also, this clearance will be the basis for further FDA submissions for HeartBeam, so it’s the cornerstone of our efforts. The 3D VECG approach is an excellent platform for AI algorithms. In the longer run, we believe that applying AI algorithms on top of the rich VECG data could result in unsurpassed predictive and diagnostic capabilities. Our landmark study, published in JACC: Advances in August of last year, showed that the AIMIGo VECG technology had similar diagnostic ability as a 12-lead ECG in detecting coronary occlusions.

Adding a baseline reading for comparison, which is a crucial part of our system, resulted in significantly better accuracy than a single 12-lead ECG. We have a 510(k) application under review with the FDA for our AIMIGo 3D VECG system. This is the cornerstone submission for HeartBeam and will be the basis of future regulatory efforts. The system includes the AIMIGo device, a patient application, a physician portal and wireless communications among the elements. We submitted our 510(k) application in the second quarter of 2023. The review remains active with FDA as we have successfully passed the acceptance of the filing and have completed the initial substantive review phase with questions and requests from FDA. We have conducted the agreed-upon testing to address FDA’s open questions and are in the process of finalizing our official responses.

Once these are submitted, the FDA will complete their review. Our timeline remains on track and we anticipate clearance by the end of Q2 2024, followed by a limited launch of AIMIGo by the end of 2024. Following the clearance of the AIMIGo 3D VECG system, we will be working to obtain a second FDA clearance focused on the ability to offer to the physician a pair of baseline and symptomatic 12-lead ECGs, both of which are synthesized from the 3D VECG signals. This second 510(k) application is planned to be submitted to FDA by Q3 2024. A key part of this submission will be a pivotal study, our valid ECG study. As we announced in March, we’ve enrolled the first patients in this pivotal study, which is designed to validate the AIMIGo 12-lead ECG synthesis software by comparing its results with those of a standard hospital-based FDA-cleared 12-lead ECG using both quantitative and qualitative assessment methodologies.

The primary objective is to demonstrate the similarities of ECG waveforms between AIMIGo’s synthesized 12-lead ECG and a standard 12-lead ECG recorded simultaneously in each subject by assessing intervals and amplitudes. In preparation for this pivotal study, we completed an 80-patient pilot study, which mirrors the pivotal study. And based on these pilot results, we plan to enroll a total of approximately 198 adult patients. Currently, we have enrolled more than 50% of the patients. We anticipate completion of enrollment of the valid ECG study in Q2 2024 in submission of the second 510(k) application by Q3 2024. As we’ve discussed on previous conference calls, we have an active AI program underway. We have acquired approximately 1 million 12-lead ECGs from various sources, a key element in our fast-paced AI development efforts.

We have developed initial deep learning algorithms focused on the ability to detect various cardiac arrhythmias. HeartBeam has had data on its deep learning algorithm accepted for presentation at two prestigious electrophysiology conferences. We believe that when combined with our credit card-size AIMIGo 3D VECG technology, HeartBeam’s AI will provide additional value to patients and physicians in a number of ways, including automated classification of cardiac conditions, the potential to further enhance the user experience and simplify the onboarding process, and in the longer run, could result in unsurpassed predictive and diagnostic capabilities. The first scientific presentation on the company’s deep learning algorithm, HeartBeam AI, was at the European Heart Rhythm Association conference in April.

Results were presented by Dr. Vivek Reddy, Director of Cardiac Arrhythmia Services at the Mount Sinai Hospital. The study showed that HeartBeam AI combined with VCG delivers equivalent performance to a 12-lead ECG and greatly improves detection of atrial flutter over a single-lead ECG. This presents an opportunity for a VCG-based algorithm that offers arrhythmia detection capabilities beyond what is available today. And to fill gaps in healthcare inequality when obtaining a 12-lead ECG is challenging. Additional data on our deep learning algorithm will be presented at the Heart Rhythm Society conference to be held in Boston next week. I’d like to now turn the call over to our Consulting CFO, Rick Brounstein.

Rick Brounstein: Thank you, Rob. I will now give a brief review of our financial results. A full breakdown is available in our regulatory filings and the press release that crossed the wire after market closed today. General and administrative expenses for the first quarter of 2024 were $2.4 million, compared to $2.5 million for the first quarter of 2023. Research and development expenses for the first quarter of 2024 were $2.4 million, compared to $1.7 million for the first quarter of 2023. The net loss for the first quarter of 2024 was $4.6 million, compared to a net loss of $4.1 million for the first quarter of 2023. Our cash and cash equivalents totaled $12.6 million as of March 31st, compared to $16.2 million as of December 31, 2023.

Net cash used in operations was $3.5 million for the three months ended March 31, 2024. We remain confident that we have sufficient funds to deliver on our milestones and get prepared to move into the commercialization phase of HeartBeam AIMIGo. I will now turn the call back over to Branislav for his closing thoughts.

Branislav Vajdic: Thanks, Rick. So, in conclusion, this is an exciting time for HeartBeam and 2024 is a pivotal year in our company evolution. I want to reiterate that our FDA clearance of the AIMIGo system will be foundational for the company. When cleared, it will be the first patient health 3D ECG device to be cleared by the FDA. It will be also serving as a robust and IP-protected foundation for many future developments. We have made significant progress on the AIMIGo clearance, having successfully passed the acceptance of the filing and have completed the initial substantive review phase. We have taken advantage of all available regulatory tools and opportunities to work interactively with the FDA and we are finalizing our testing and our formal responses to the questions raised by the FDA.

Once these responses are submitted in the near future, the FDA will complete their review. We continue to anticipate clearance by the end of Q2 of this year. This initial clearance is foundational for a number of reasons. First, it will be the basis of our second submission on the algorithm that generates the 12-lead synthesized waveform. Currently, we have enrolled more than 50% of the patients in the valid ECG study. We will submit the results of this pivotal study to the FDA as a key element of this 12-lead synthesis submission. Second, we are developing deep learning algorithms using the 3D ECG signals for inputs. We presented at the European Heart Rhythm Association conference, making the first scientific presentation on HeartBeam AI, and look forward to the second presentation at the HeartBeam Society meeting in Boston next week.

Finally, we will build upon the initial AIMIGo clearance as a foundation. With both the 12-lead synthesis algorithms and AI efforts, we will continue to advance our robust product pipeline from AI-intensive advances to expanding indications to patient-friendly form factors, such as the on-demand 12-lead patch and our 12-lead watch. We believe that our VCG technology has the potential to be the most advanced ambulatory cardiac monitoring solution and is applicable in a number of form factors. In anticipation of the FDA clearance, we are refining our go-to-market strategy and are encouraged by our early discussions with industry partners and their interest in our technology. We ended the quarter of this year with $2000 -- $12.6 million in cash and cash equivalents.

So that is $12.6 million in cash and cash equivalents. We remain confident that we have sufficient funds to deliver on our timelines. I look forward to providing our shareholders with further updates in the near future. I thank you all for attending. And now, the HeartBeam team would like to answer your questions. Operator?

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