AVITA Medical Reports First Fiscal Quarter 2022 Financial Results
AVITA Medical (RCEL) reported a 39% increase in first-quarter revenue, reaching $7.0 million, up from $5.1 million in Q1 2021. Gross profit margin improved to 85% from 82%. Operating expenses decreased by 18% to $12.3 million, leading to a reduced net loss of $5.9 million ($0.24 per share), down from a loss of $10.2 million ($0.48 per share) last year. The company continues to face challenges due to hospital staffing shortages but sees ongoing enrollment in its soft tissue reconstruction trial. Revenue guidance for Q2 2022 remains at approximately $7.0 million.
- Revenue increased by 39% to $7.0 million.
- Gross profit margin improved to 85%.
- Operating expenses decreased by 18% to $12.3 million.
- Net loss reduced by 42% to $5.9 million.
- Hospital staffing shortages impacted RECELL usage in burn procedures.
- Q2 2022 revenue guidance remains at $7.0 million due to ongoing pandemic uncertainty.
VALENCIA, Calif. and MELBOURNE, Australia, Nov. 08, 2021 (GLOBE NEWSWIRE) -- AVITA Medical, Inc. (NASDAQ: RCEL, ASX:AVH) (the “Company”), a regenerative medicine company that is developing and commercializing a technology platform that enables point-of-care autologous skin restoration for multiple unmet needs, today reported financial results for its first fiscal quarter ended September 30, 2021.
First Quarter Fiscal Year 2022 Highlights
- Total revenue increased
39% to$7.0 million compared to$5.1 million in the first fiscal quarter of 2021 - Gross profit margin improved
3% to85% compared to the first fiscal quarter of 2021 - Total operating expenses decreased
18% to$12.3 million compared to$14.9 million in the first fiscal quarter of 2021 - Net loss of
$5.9 million , or$0.24 per share compared to a net loss of$10.2 million , or$0.48 per share in the first fiscal quarter of 2021 - As of September 30, 2021, the Company had
$60.4 million in cash and cash equivalents and$49.5 million in short-term and long-term marketable securities, and no debt
“I am pleased with the progress we made in the overall business this quarter, despite the hospital staffing shortages that impeded RECELL usage in burn procedures,” said Dr. Mike Perry, AVITA Medical Chief Executive Officer. “We saw continued acceleration of enrollment into our soft tissue reconstruction trial, which is now close to completion with 58 of 65 subjects. We look forward to expanding into this
First Quarter of Fiscal Year 2022 Financial Results
Total revenue for the three months ended September 30, 2021, was
Gross profit margin for the three months ended September 30, 2021, was
Total operating expenses for the three months ended September 30, 2021, was
Second Quarter of Fiscal Year 2022 Revenue Guidance
- Total revenue is expected to be approximately
$7.0 million . This guidance reflects the anticipated impact of hospital staffing challenges as well uncertainty with the pandemic.
Webcast and Conference Call Information
The Company will host a conference call to discuss the first quarter financial results after market close on Monday, November 8, 2021, at 1:30 p.m. Pacific Time / 4:30 p.m. Eastern Time (being 8.30 a.m. Australian Eastern Daylight Time on Tuesday, November 9, 2021). The conference call can be accessed live over the phone at (833) 614-1538 for U.S. callers or at (706) 634-6548 international callers, using conference ID:2592487. The live webinar can be accessed at https://ir.avitamedical.com.
Authorized for release by the Chief Financial Officer of AVITA Medical, Inc.
ABOUT AVITA Medical, Inc.
AVITA Medical, Inc. is a regenerative medicine company with a technology platform positioned to address unmet medical needs in burns, chronic wounds, and aesthetics indications. AVITA Medical Inc. patented and proprietary collection and application technology provides innovative treatment solutions derived from the regenerative properties of a patient’s own skin. The medical devices work by preparing a RES® REGENERATIVE EPIDERMAL SUSPENSION, an autologous suspension comprised of the patient’s skin cells necessary to regenerate natural healthy epidermis. This autologous suspension is then sprayed onto the areas of the patient requiring treatment.
AVITA Medicals’ first U.S. product, the RECELL® System, was approved by the U.S. Food and Drug Administration (FDA) in September 2018. The RECELL® System is approved for acute partial-thickness thermal burn wounds in patients 18 years of age and older or application in combination with meshed autografting for acute full-thickness thermal burn wounds in pediatric and adult patients. The RECELL® System is used to prepare Spray-On Skin™ Cells using a small amount of a patient’s own skin, providing a new way to treat severe burns, while significantly reducing the amount of donor skin required. The RECELL® System is designed to be used at the point of care alone or in combination with autografts depending on the depth of the burn injury. Compelling data from randomized, controlled clinical trials conducted at major U.S. burn centers and real-world use in more than 8,000 patients globally, reinforce that the RECELL® System is a significant advancement over the current standard of care for burn patients and offers benefits in clinical outcomes and cost savings. Healthcare professionals should read the INSTRUCTIONS FOR USE - RECELL® Autologous Cell Harvesting Device (https://recellsystem.com/) for a full description of indications for use and important safety information including contraindications, warnings, and precautions.
In international markets, our products are marketed under the RECELL® System brand to promote skin healing in a wide range of applications including burns, chronic wounds, and aesthetics. The RECELL® System is TGA-registered in Australia and received CE-mark approval in Europe.
To learn more, visit www.avitamedical.com.
CAUTIONARY NOTE REGARDING FORWARD-LOOKING STATEMENTS
This press release includes forward-looking statements. These forward-looking statements generally can be identified by the use of words such as “anticipate,” “expect,” “intend,” “could,” “may,” “will,” “believe,” “estimate,” “look forward,” “forecast,” “goal,” “target,” “project,” “continue,” “outlook,” “guidance,” “future,” other words of similar meaning and the use of future dates. Forward-looking statements in this press release include, but are not limited to, statements concerning, among other things, our ongoing clinical trials and product development activities, regulatory approval of our products, the potential for future growth in our business, and our ability to achieve our key strategic, operational, and financial goals. Forward-looking statements by their nature address matters that are, to different degrees, uncertain. Each forward- looking statement contained in this press release is subject to risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statement. Applicable risks and uncertainties include, among others, the timing of regulatory approvals of our products; physician acceptance, endorsement, and use of our products; failure to achieve the anticipated benefits from approval of our products; the effect of regulatory actions; product liability claims; risks associated with international operations and expansion; and other business effects, including the effects of industry, economic or political conditions including, but not limited to the ongoing COVID-19 pandemic which are outside of the company’s control. Investors should not place considerable reliance on the forward-looking statements contained in this press release. Investors are encouraged to read our publicly available filings for a discussion of these and other risks and uncertainties. The forward-looking statements in this press release speak only as of the date of this release, and we undertake no obligation to update or revise any of these statements.
FOR FURTHER INFORMATION:
U.S. Media Sam Brown, Inc. Christy Curran Phone +1 615 414 8668 christycurran@sambrown.com O.U.S Media Monsoon Communications Rudi Michelson Phone +61 (0)3 9620 3333 Mobile +61 (0)411 402 737 rudim@monsoon.com.au | Investors ICR Westwicke Caroline Corner Phone +1 415 202 5678 caroline.corner@westwicke.com |
AVITA MEDICAL, INC.
Consolidated Balance Sheets
(In thousands, except share and per share data)
(Unaudited)
As of | ||||||||
September 30, 2021 | June 30, 2021 | |||||||
ASSETS | ||||||||
Cash and cash equivalents | $ | 60,484 | $ | 110,746 | ||||
Marketable securities | 29,703 | - | ||||||
Accounts receivable, net | 3,118 | 3,467 | ||||||
BARDA receivables | 603 | 3,936 | ||||||
Prepaids and other current assets | 1,129 | 1,333 | ||||||
Restricted cash | 201 | 201 | ||||||
Inventory | 1,892 | 1,647 | ||||||
Total current assets | 97,130 | 121,330 | ||||||
Marketable securities, long-term | 19,801 | |||||||
Plant and equipment, net | 1,357 | 1,458 | ||||||
Operating lease right-of-use assets | 1,710 | 1,480 | ||||||
Intangible assets, net | 472 | 472 | ||||||
Other long-term assets | 703 | 761 | ||||||
Total assets | $ | 121,173 | $ | 125,501 | ||||
LIABILITIES AND SHAREHOLDERS' EQUITY | ||||||||
Accounts payable and accrued liabilities | 2,439 | 3,120 | ||||||
Accrued wages and fringe benefits | 3,663 | 3,321 | ||||||
Other current liabilities | 951 | 949 | ||||||
Total current liabilities | 7,053 | 7,390 | ||||||
Contract liabilities | 1,018 | 1,075 | ||||||
Operating lease liabilities, long term | 1,107 | 878 | ||||||
Other long-term liabilities | 503 | 503 | ||||||
Total liabilities | 9,681 | 9,846 | ||||||
Contingencies (Note 10) | ||||||||
Shareholders' Equity: | ||||||||
Common stock, | 3 | 3 | ||||||
Preferred stock, | - | - | ||||||
Additional paid-in capital | 330,734 | 328,889 | ||||||
Accumulated other comprehensive income | 8,199 | 8,259 | ||||||
Accumulated deficit | (227,444 | ) | (221,496 | ) | ||||
Total shareholders' equity | 111,492 | 115,655 | ||||||
Total liabilities and shareholders' equity | $ | 121,173 | $ | 125,501 | ||||
The accompanying notes form part of the consolidated financial statements | ||||||||
AVITA MEDICAL, INC.
Consolidated Statements of Operations
(In thousands, except share and per share data)
(Unaudited)
Three Months Ended September 30, | ||||||||
2021 | 2020 | |||||||
Revenues | $ | 7,020 | $ | 5,060 | ||||
Cost of sales | (1,088 | ) | (929 | ) | ||||
Gross profit | 5,932 | 4,131 | ||||||
BARDA income | 374 | 596 | ||||||
Operating expenses: | ||||||||
Sales and marketing expenses (1) | (3,518 | ) | (3,265 | ) | ||||
General and administrative expenses (1) | (5,349 | ) | (8,302 | ) | ||||
Research and development expenses (1) | (3,388 | ) | (3,374 | ) | ||||
Total operating expenses | (12,255 | ) | (14,941 | ) | ||||
Operating loss | (5,949 | ) | (10,214 | ) | ||||
Interest expense | (9 | ) | (7 | ) | ||||
Other income | 16 | 4 | ||||||
Loss before income taxes | (5,942 | ) | (10,217 | ) | ||||
Income tax expense | (6 | ) | (10 | ) | ||||
Net loss | $ | (5,948 | ) | $ | (10,227 | ) | ||
Net loss per common share: | ||||||||
Basic | $ | (0.24 | ) | $ | (0.48 | ) | ||
Diluted | $ | (0.24 | ) | $ | (0.48 | ) | ||
Weighted-average common shares: | ||||||||
Basic | 24,905,403 | 21,503,643 | ||||||
Diluted | 24,905,403 | 21,503,643 |
(1) Total operating expenses include impact of share-based compensation as follows:
Three-months ended September 30, | ||||||
2021 | 2020 | |||||
Sales and marketing expenses | $ | 291 | $ | 330 | ||
General and administrative expenses | 1,251 | 2,766 | ||||
Research and development expenses | 300 | 170 | ||||
Total | $ | 1,842 | $ | 3,266 |
FAQ
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