- Successfully Met Clinical Endpoints in the VALID-ECG Pivotal
Study Showing 93.4% Overall Diagnostic Agreement for Assessment of
Arrhythmia
- Productive Discussions with FDA on 510(k) Submission for
Groundbreaking 12-lead Electrocardiogram (ECG) Synthesis
Software
- Signed Strategic Collaboration with AccurKardia to Enhance
Commercial Offering for Arrhythmia Assessment
- Added Two New US Patents to Robust IP Portfolio and
Differentiated Position in Remote Cardiac Diagnostics
- Management to Host Webcast and Conference Call Today at 4:30
p.m. ET
HeartBeam, Inc. (NASDAQ: BEAT), a medical technology
company focused on transforming cardiac care by providing powerful
personalized insights, has reported its financial and operational
results for the first quarter ended March 31, 2025.
First Quarter & Subsequent 2025 Operational
Highlights
The Company continues to make significant progress towards
commercial readiness with key clinical and regulatory achievements
on the HeartBeam System.
VALID-ECG Pivotal Study:
- Successfully met the clinical endpoints in the VALID-ECG
pivotal study, which enrolled 198 patients across five (5) US sites
for arrhythmia assessment.
- Data showed a 93.4% overall diagnostic agreement, indicating
that the synthesized 12-lead ECG can support diagnosis of
arrhythmias in a manner consistent with standard 12-lead ECGs.
- Data was presented by Thomas Deering, M.D., of Piedmont Heart
Institute, at the Heart Rhythm Society (HRS) meeting in April 2025
and showed that the study met its performance goals.
- Study formed the basis of the US Food and Drug Administration
(FDA) 510(k) submission for 12-lead ECG synthesis software for
arrhythmia assessment.
12-Lead ECG Synthesis Software FDA Submission:
- Received foundational FDA 510(k) clearance of the HeartBeam
System, which captures the heart’s electrical signals in 3D (by
capturing 3 non-coplanar directions), for comprehensive arrhythmia
assessment in December 2024.
- Submitted FDA 510(k) application focused on the patented
HeartBeam software that converts the heart’s electrical signals
captured in 3 non-coplanar directions into a synthesized 12-lead
ECG in January 2025.
- Ongoing productive discussions with FDA related to the 510(k)
application throughout the quarter.
- Combined with the VALID-ECG results, these interactions provide
confidence that the stated timeline for FDA clearance remains
intact.
Commercial Readiness Plans:
- Anticipate initiating commercialization upon receiving 510(k)
clearance for the 12-lead ECG synthesis software.
- Commenced an Early Access Program to obtain important feedback
on the end-to-end clinical workflow, ensure operational readiness
and establish an early adopter funnel in anticipation of US
commercialization.
- Signed contract manufacturer with ability to scale production
alongside Company growth.
- Finalized strategic collaboration with AccurKardia, an
innovator in ECG-based diagnostics technology, focusing on making
AccurKardia’s FDA-cleared ECG analysis software, AccurECG™,
available on HeartBeam’s devices.
Other Highlights:
- Closed a public offering of common stock with gross proceeds of
approximately $11.5 million in February 2025, including the
exercise of the underwriter’s over-allotment option, to fund key
growth milestones and preparation for US commercialization.
- Received two new US patents, and now owns 20 issued US and
international patents, as well as two (2) allowed patents and 32
pending patents, adding to an already robust IP portfolio that
supports the company’s differentiated position in remote cardiac
diagnostics.
- Appointed Chief Executive Officer, Robert Eno, to the Board of
Directors.
- Appointed Dr. Vivek Reddy of Mount Sinai, one of the nation’s
premier cardiac electrophysiologists, to the HeartBeam Scientific
Advisory Board.
- Cash, cash equivalents, and short-term investments totaled $8.2
million as of March 31, 2025, with net cash used in operating
activities of $4.5 million for the three months ended March 31,
2025.
Management Commentary
“The first quarter of 2025 demonstrated continued progress on
commercial readiness plans, underscored by successful pivotal study
results, a new strategic partnership, and strengthened intellectual
property protection,” said Robert Eno, Chief Executive Officer,
HeartBeam.
“Since submitting a 510(k) application to the FDA for the
12-lead ECG synthesis software designed for the assessment of
arrhythmias, we have had ongoing productive discussions with the
FDA. The submission is backed by robust data demonstrating
HeartBeam successfully met the clinical endpoints in the VALID-ECG
pivotal study. This important milestone confirms that our
technology has the ability to deliver 12-lead ECG-like insights
through the convenience of a credit card-sized device that patients
can use whenever arrhythmia symptoms occur.
“We recently partnered with AccurKardia, an innovator in
ECG-based diagnostics technology, to add its FDA-cleared ECG
analysis software, AccurECG, to our devices. We believe combining
our platforms will enhance our commercial offering for arrhythmia
assessment by enabling patients and physicians to get an automated
rhythm assessment. This will facilitate quicker diagnosis and
faster access to clinical care when needed. The strategic
collaboration is expected to expedite our product development
efforts, reducing both costs and timelines.
“We received two new US patents to bolster the defensive and
offensive moat around our core technology. The first patent
significantly advances intellectual property for our credit
card-sized ECG device, and the second patent expands the use of
risk-based diagnostic algorithms into our product portfolio around
wearable devices. We now own 20 issued patents worldwide, cementing
our leadership in cardiac monitoring innovation.
“Looking ahead, we are focused on commercial readiness
activities and key growth milestones, leveraging gross proceeds of
approximately $11.5 million from the recent fundraising we
completed during the quarter. With productive discussions with the
FDA on our 12-lead ECG synthesis software submission, we believe
our timeline for clearance remains intact. We also commenced
initial FDA interactions on expanding our indication to include
ischemia and acute coronary events such as heart attacks. We expect
to start enrollment in a Pilot Study on this indication in the
second half of 2025. Taken together, we are advancing steadily on
our milestones and look forward to additional updates in the months
to come,” concluded Eno.
First Quarter 2025 Financial Results
Research and development expenses for the first quarter of 2025
were $3.5 million, compared to $2.4 million for the first quarter
of 2024.
General and administrative expenses for the first quarter of
2025 were $2.0 million compared to $2.4 million for the first
quarter of 2024.
Net loss for the first quarter of 2025 was $5.5 million,
compared to a net loss of $4.6 million for the first quarter of
2024.
Net cash used in operating activities was $4.5 million for the
three months ended March 31, 2025, as compared to $3.5 million for
the first quarter of 2024.
Cash, cash equivalents, and short-term investments totaled $8.2
million as of March 31, 2025, compared to $2.4 million as of
December 31, 2024. On February 25, 2025, the Company closed a
public offering of common stock with gross proceeds of $11.5
million in February 2025, including the exercise of the
underwriter’s over-allotment option.
First Quarter 2025 Results Conference Call
HeartBeam CEO Robert Eno and CFO Tim Cruickshank will host the
conference call, followed by a question-and-answer period. The
conference call will be accompanied by a presentation, which can be
viewed during the webcast or accessed via the investor relations
section of the Company’s website here.
To access the call, please use the following information:
Date:
Tuesday, May 13, 2025
Time:
4:30 p.m. Eastern time (1:30 p.m. Pacific
time)
Dial-in:
1-844-826-3035
International Dial-in:
1-412-317-5195
Conference Code:
10199007
Webcast:
HeartBeam First Quarter 2025 Earnings
Conference Call
A telephone replay will be available approximately three hours
after the call and will run through August 13, 2025, by dialing
1-844-512-2921 from the U.S., or 1-412-317-6671 from international
locations, and entering replay pin number: 10199007. The replay can
also be viewed through the webcast link above and the presentation
utilized during the call will be available in the Company’s
investor relations section here.
About HeartBeam, Inc.
HeartBeam, Inc. (NASDAQ: BEAT) is a medical technology company
dedicated to transforming the detection and monitoring of critical
cardiac conditions. The Company is creating the first ever
cable-free device capable of collecting ECG signals in 3D, from 3
non-co-planar directions, and synthesizing the signals into a
12-lead ECG. This platform technology is designed for portable
devices that can be used wherever the patient is to deliver
actionable heart intelligence. Physicians will be able to identify
cardiac health trends and acute conditions and direct patients to
the appropriate care – all outside of a medical facility, thus
redefining the future of cardiac health management. HeartBeam’s 3D
ECG technology received FDA clearance for arrhythmia assessment in
December 2024. The Company holds 20 issued patents related to
technology enablement. For additional information, visit
HeartBeam.com.
Forward-Looking Statements
All statements in this release that are not based on historical
fact are "forward-looking statements." While management has based
any forward-looking statements included in this release on its
current expectations, the information on which such expectations
were based may change. Forward-looking statements involve inherent
risks and uncertainties which could cause actual results to differ
materially from those in the forward-looking statements, as a
result of various factors including those risks and uncertainties
described in the Risk Factors and in Management’s Discussion and
Analysis of Financial Condition and Results of Operations sections
of our Forms 10-K, 10-Q and other reports filed with the SEC and
available at www.sec.gov. We urge you to consider those risks and
uncertainties in evaluating our forward-looking statements. We
caution readers not to place undue reliance upon any such
forward-looking statements, which speak only as of the date made.
Except as otherwise required by the federal securities laws, we
disclaim any obligation or undertaking to publicly release any
updates or revisions to any forward-looking statement contained
herein (or elsewhere) to reflect any change in our expectations
with regard thereto or any change in events, conditions or
circumstances on which any such statement is based.
HEARTBEAM, INC.
Condensed Balance Sheets
(Unaudited)
(In thousands, except share
data)
March 31, 2025
December 31,
2024
Assets
Current Assets:
Cash and cash equivalents
$
4,390
$
2,377
Short-term investments
3,760
—
Prepaid expenses and other current
assets
458
393
Total Current Assets
8,608
2,770
Property and equipment, net
443
450
Other assets
56
56
Total Assets
$
9,107
$
3,276
Liabilities and Stockholders’
Equity
Current Liabilities:
Accounts payable (includes related party
$5 and $5, respectively)
$
523
$
531
Accrued expenses
1,055
1,091
Total Current Liabilities
1,578
1,622
Total Liabilities
1,578
1,622
Commitments
Stockholders’ Equity
Preferred stock - $0.0001 par value;
10,000,000 authorized; 0 shares outstanding at March 31, 2025 and
December 31, 2024
—
—
Common stock - $0.0001 par value
100,000,000 shares authorized; 33,734,548 and 26,960,901 shares
issued and outstanding at March 31, 2025 and December 31, 2024,
respectively
3
3
Additional paid in capital
69,283
57,924
Accumulated deficit
(61,757
)
(56,273
)
Total Stockholders’ Equity
7,529
1,654
Total Liabilities and Stockholders’
Equity
$
9,107
$
3,276
HEARTBEAM, INC.
Condensed Statements of
Operations (Unaudited)
(In thousands, except share
and per share data)
Three months ended March
31,
2025
2024
Operating Expenses:
General and administrative
$
2,012
$
2,356
Research and development
3,492
2,428
Total operating expenses
5,504
4,784
Loss from operations
(5,504
)
(4,784
)
Other Income and (Expense)
Interest income
20
178
Total other income
20
178
Loss before provision for income taxes
(5,484
)
(4,606
)
Income tax provision
—
—
Net Loss
$
(5,484
)
$
(4,606
)
Net loss per share, basic and diluted
$
(0.18
)
$
(0.17
)
Weighted average common shares
outstanding, basic and diluted
30,378,751
26,511,201
HEARTBEAM, INC.
Condensed Statements of Cash
Flows (Unaudited)
(In thousands)
Three months ended March
31,
2025
2024
Cash Flows From Operating
Activities
Net loss
$
(5,484
)
$
(4,606
)
Adjustments to reconcile net loss to net
cash used in operating activities
Depreciation
7
—
Stock based compensation expense
1,109
1,207
Changes in operating assets and
liabilities:
Prepaid expenses and other current
assets
(65
)
33
Accounts payable and accrued expenses
(44
)
(97
)
Net cash used in operating
activities
(4,477
)
(3,463
)
Cash Flows From Investing
Activities
Purchase of property and equipment
—
(88
)
Purchase of short-term investments
(3,760
)
—
Net cash used in investing
activities
(3,760
)
(88
)
Cash Flows From Financing
Activities
Proceeds from sale of equity, net of
issuance costs
10,250
—
Net cash provided by financing
activities
10,250
—
Net increase (decrease) in cash and
restricted cash
2,013
(3,551
)
Cash, cash equivalents and restricted
cash – Beginning of period
2,433
16,239
Cash, cash equivalents and restricted
cash – Ending of period
$
4,446
$
12,688
Reconciliation of cash, cash
equivalents and restricted cash:
Cash and cash equivalents
$
4,390
$
12,638
Restricted cash (included in other
assets)
56
50
Total cash, cash equivalents and
restricted cash
$
4,446
$
12,688
Supplemental Disclosures of Cash Flow
Information:
Purchase of property and equipment in
accounts payable
$
2
$
—
View source
version on businesswire.com: https://www.businesswire.com/news/home/20250513490910/en/
Investor Relations Contact: Chris Tyson Executive Vice
President MZ North America Direct: 949-491-8235 BEAT@mzgroup.us
www.mzgroup.us
Media Contact:media@heartbeam.com
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