Full Press Release Details
Air Reports Fiscal Third Quarter 2025 Financial Results and Provides Corporate Update
increased 34% compared to the previous quarter ended September 30, 2024; and exceeded $1 million
CE Mark for LungFit PH in Europe and Market Authorization in Australia; international shipments to commence later
call at 4:30 p.m. ET today, February 10th
City, NY, February 10, 2025 - Beyond Air, Inc. (NASDAQ: XAIR) ("Beyond Air" or the "Company"),
a commercial stage medical device and biopharmaceutical company focused on harnessing the power of nitric oxide (NO) to improve the lives
of patients, today announced its financial results for the fiscal third quarter ended December 31, 2024, and provided a corporate update.
commercial team continues to make significant progress as we expand the number of U.S. hospitals utilizing LungFit PH. While this is
the culmination of years of work, it was approximately nine months ago that we started to make significant headway in our commercial
efforts with the fully updated system. We expect to continue generating double digit sequential quarterly revenue growth for the foreseeable
future," said Steve Lisi, Chairman and Chief Executive Officer of Beyond Air.
ended calendar year 2024 on a high note with the receipt of CE Mark for LungFit PH in Europe, opening a significant portion of the global
market outside of the U.S. for our current and future distribution partners to launch their commercial programs for LungFit PH. With
the advantage of real-world customer experience and feedback from our U.S. program, combined with our distribution partners' established
sales teams and customer networks, we anticipate a faster commercial ramp-up in these regions compared to what we experienced in the
U.S.," concluded Mr. Lisi.
Execution, Portfolio Highlights and Upcoming Milestones
| A 34% increase in revenue for the quarter ended December 31, 2024, compared with the quarter ended September 30, 2024 | ||
| Six new hospital starts in the U.S. in the quarter ended December 31, 2024 |
| Received market authorization in Australia in January 2025 and expect to have regulatory approvals in eight countries covered under the partnership with Getz Healthcare by calendar year-end, with initial commercial shipments occurring in 2025. | ||
| Signed partnerships with two distributors in the Middle East in January 2025, with initial shipments expected in the 1H of calendar year 2025. |
| The treatment of infants > 34 weeks gestation with hypoxic respiratory failure associated with clinical or echocardiographic evidence of pulmonary hypertension, in order to improve oxygenation and to reduce the need for extracorporeal membrane oxygenation; and | ||
| The treatment of peri- and post-operative pulmonary hypertension in adults and newborn infants, infants and toddlers, children and adolescents, ages 0-17 years in conjunction to heart surgery, in order to selectively decrease pulmonary arterial pressure and improve right ventricular function |
| Currently no FDA approved nitric oxide system is labeled for cardiac surgery | ||
| Approval should increase LungFit PH's rate of market penetration |
Cancer - Solid Tumor Program
| Phase 1a trial (monotherapy) - Part A of the trial evaluating ultra-high concentration Nitric Oxide (UNO) therapy in subjects with advanced, relapsed or refractory unresectable, primary or metastatic cutaneous and subcutaneous solid tumors at a dose of 25,000 ppm has been completed, and at the dose of 50,000 ppm is ongoing. | ||
| Phase 1b trial (combination therapy) - Received regulatory approval in Israel for Part B of the trial, which will assess the intratumoral administration of 25,000 ppm low volume (LV) Nitric Oxide (UNO) in patients with unresectable cutaneous or subcutaneous histologically confirmed primary or metastatic lesions, who have shown disease progression or prolonged stable disease (12 weeks) after receiving a single agent anti-PD-1 containing treatment. Topline data from the Phase 1b portion of the study are anticipated late in calendar 2025 or early-2026. |
- Autism Spectrum Disorder (ASD) Program
Results for the Fiscal Third Quarter Ended December 31, 2024
for the fiscal quarter ended December 31, 2024 were $1.1 million compared to $0.4 million for the fiscal quarter ended December 31, 2023
and $0.8 million for the previous quarter ended September 30, 2024.
of revenue of $1.3 million was recognized for the three months ended December 31, 2024, compared to $0.7 million for the three months
ended December 31, 2023. Cost of revenue exceeded revenue primarily driven by depreciation of LungFit devices and one-time upgrade costs
and development expenses for the three months ended December 31, 2024 were $3.0 million as compared to $6.8 million for the three months
ended December 31, 2023. The decrease of $3.8 million was primarily attributed to a decrease in salaries, stock-based compensation and
to a lesser extent from clinical and pre-clinical studies expenses.
general and administrative expenses for the three-month periods ended December 31, 2024 and 2023 were $7.7 million and $9.8 million,
respectively. The decrease of $2.1 million was attributed primarily to a reduction in salaries and stock-based compensation cost.
expense for the three months ended December 31, 2024 was $2.4 million compared to $0.3 million for the three months ended December 31,
2023. The increase in other expense of $2.1 million was mainly due to a non-cash loss recorded upon the retirement of the Avenue Capital
burn in the fiscal quarter ended December 31, 2024, excluding the impacts of financing and the extinguishment of debt, was $7.6 million.
of December 31, 2024, the Company reported cash, cash equivalents, and marketable securities of $10.9 million, and total debt outstanding
of $11.8 million. Debt repayment does not begin until October 2026. The Company's cash, cash equivalents, and marketable securities,
along with its cash conservation strategy and anticipated revenue growth are expected to provide sufficient cash runway to support current
operating plans well into calendar 2026.
| Monday, February 10 th @ 4:30 PM ET | |
| Domestic: | 1-877-407-0784 |
| International: | 1-201-689-8560 |
| Conference ID: | 13750714 |
| Webcast: | A webcast of the live conference call can be accessed by visiting the Events section of the Company's website (click here) or directly (click here). An online recording of the conference call will be available on the Company's website or via the direct link an hour after the call. |
Air is a commercial stage medical device and biopharmaceutical company dedicated to harnessing the power of endogenous and exogenous
nitric oxide (NO) to improve the lives of patients suffering from respiratory illnesses, neurological disorders, and solid tumors. The
Company has received FDA approval for its first system, LungFit PH, for the treatment of term and near-term neonates with hypoxic
respiratory failure. Beyond Air is currently advancing its other revolutionary LungFit systems in clinical trials for the treatment of
severe lung infections such as viral community-acquired pneumonia (including COVID-19), and nontuberculous mycobacteria (NTM) among others.
Also, the Company has also partnered with The Hebrew University of Jerusalem to advance a pre-clinical program dedicated to the treatment
of autism spectrum disorder (ASD) and other neurological disorders. Additionally, Beyond Cancer, Ltd., an affiliate of Beyond Air, is
investigating ultra-high concentrations of NO with a proprietary delivery system to target certain solid tumors in the pre-clinical setting.
For more information, visit www.beyondair.net.
Air's LungFit is a cylinder-free, phasic flow generator and delivery system and has been designated as a medical device by the
U.S. Food and Drug Administration (FDA). The ventilator compatible version of the device can generate NO from ambient air on demand for
delivery to the lungs at concentrations ranging from 1 ppm to 80 ppm. The LungFit system could potentially replace large, high-pressure
NO cylinders providing significant advantages in the hospital setting, including greatly reducing inventory and storage requirements,
improving overall safety with the elimination of NO2 purging steps, and other benefits. LungFit can also deliver NO at concentrations
at or above 80 ppm for potentially treating severe acute lung infections in the hospital setting (e.g. COVID-19, bronchiolitis)
and chronic, refractory lung infections in the home setting (e.g. NTM). With the elimination of cylinders, Beyond Air intends
to offer NO treatment in the home setting.
Air's LungFit PH is approved for commercial use in the United States of America, European Union, Australia and New Zealand. Beyond
Air's other LungFit systems are not approved for commercial use and are for investigational use only. Beyond Air is not suggesting
NO use over 80 ppm or use at home.
pulmonary hypertension of the newborn (PPHN) is a lethal condition and secondary to failure of normal circulatory transition at birth.
It is a syndrome characterized by elevated pulmonary vascular resistance (PVR) that causes labile hypoxemia due to decreased pulmonary
blood flow and right-to-left shunting of blood. Its incidence has been reported as 1.9 per 1000 live births (0.4-6.8/1000 live
births) with mortality rate ranging between 4-33%. This syndrome complicates the course of about 10% of infants with respiratory
failure and remains a source of considerable morbidity and mortality. NO gas is a vasodilator, is approved in dozens of countries to
improve oxygenation and reduces the need for extracorporeal membrane oxygenation (ECMO) in term and near-term (>34 weeks gestation)
neonates with hypoxic respiratory failure associated with clinical or echocardiographic evidence of pulmonary hypertension in conjunction
with ventilator support and other appropriate agents.
Cancer, Ltd., an affiliate of Beyond Air, Inc., is a development-stage biopharmaceutical and medical device company utilizing (UNO via
a proprietary delivery platform to treat primary tumors and prevent metastatic disease. Nitric oxide at ultra-high concentrations has
been reported to show anticancer properties and to potentially serve as a chemosensitizer and radiotherapy enhancer. A first-in-human
study is underway in patients with solid tumors. The Company is conducting preclinical studies of UNO in multiple solid tumor models
to inform additional treatment protocols.
more information, visit www.beyondcancer.com.
press release contains "forward-looking statements" concerning the potential safety and efficacy of inhaled nitric oxide
and the ultra-high concentration nitric oxide product candidate, as well as its therapeutic potential in a number of indications; and
the potential impact on patients and anticipated benefits associated with inhaled nitric oxide and the ultra-high concentration nitric
oxide product candidate. Forward-looking statements include statements about expectations, beliefs, or intentions regarding product offerings,
business, results of operations, strategies or prospects. You can identify such forward-looking statements by the words "appears,"
"expects," "plans," "anticipates," "believes" "expects," "intends,"
"looks," "projects," "goal," "assumes," "targets" and similar expressions
and/or the use of future tense or conditional constructions (such as "will," "may," "could," "should"
and the like) and by the fact that these statements do not relate strictly to historical or current matters. Rather, forward-looking
statements relate to anticipated or expected events, activities, trends or results as of the date they are made. Because forward-looking
statements relate to matters that have not yet occurred, these statements are inherently subject to risks and uncertainties that could
cause actual results to differ materially from any future results expressed or implied by the forward-looking statements. These forward-looking
statements are only predictions and reflect views as of the date they are made with respect to future events and financial performance.
Many factors could cause actual activities or results to differ materially from the activities and results anticipated in forward-looking
statements, including risks related to the ability to raise additional capital; the timing and results of future pre-clinical studies
and clinical trials; the potential that regulatory authorities, including the FDA and comparable non-U.S. regulatory authorities, may
not grant or may delay approval for our product candidates; the approach to discover and develop novel drugs, which is unproven and may
never lead to efficacious or marketable products; the ability to fund and the results of further pre-clinical studies and clinical trials
of our product candidates; obtaining, maintaining and protecting intellectual property utilized by products; obtaining regulatory approval
for products; competition from others using similar technology and others developing products for similar uses; dependence on collaborators;
and other risks, which may, in part, be identified and described in the "Risk Factors" section of Beyond Air's most
recent Annual Report on Form 10-K and other of its filings with the Securities and Exchange Commission, all of which are available on
Beyond Air's website. Beyond Air and Beyond Cancer undertake no obligation to update, and have no policy of updating or revising,
these forward-looking statements, except as required by applicable law.