Full Press Release Details
AVITA Medical Reports First Fiscal Quarter 2022 Financial Results
VALENCIA, Calif, November 8, 2021 and MELBOURNE, Australia, November 9, 2021 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
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 $450 million serviceable addressable market upon approval, beginning with our existing burn center accounts and
leveraging our new TPT code in the outpatient setting.
First Quarter of Fiscal Year 2022 Financial Results
Total revenue for the three months ended September 30, 2021, was $7.0 million, an increase of $2.0 million or 39% over the $5.1 million
reported for the same period in 2020. The increase was largely driven by broader utilization among our customer base as well as deeper penetration within individual customer accounts.
Gross profit margin for the three months ended September 30, 2021, was 85% compared to 82% reported for the same period in 2020. Higher gross margin was
driven by lower shipping costs and increased production at our Ventura facility.
Total operating expenses for the three months ended September 30,
2021, was $12.3 million, a decrease of $2.7 million or 18% over the $14.9 million reported for the same period in 2020. The decrease in operating expenses is primarily attributable to lower stock-based compensation and higher costs in
the prior year related to the Avita group s redomiciliation to the United States, along with severance costs associated with a former executive. This was partially offset with higher travel costs in the current year due to fewer COVID-19 related travel restrictions.Net loss for the three months ended September 30, 2021 was $5.9 million, a decrease of $4.3 million, or 42%, over the $10.2 million loss recognized during the
same period last year. The decrease in net loss was driven by the lower operating expenses described above and the higher revenue during the three months ended September 30, 2021.
Second Quarter of Fiscal Year 2022 Revenue Guidance
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.
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.
Consolidated Balance Sheets
(In thousands, except share and per share data)
| 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, $0.0001 par value per share, 200,000,000 shares authorized, 24,925,118 and 24,895,864 shares issued and outstanding at September 30, 2021 and June 30, 2021, respectively | 3 | 3 | ||||||
| Preferred stock, $0.0001 par value per share, 10,000,000 shares authorized, no shares issued or outstanding at September 30, 2021 and June 30, 2021 | ||||||||
| 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
Consolidated Statements of Operations
(In thousands, except share and per share data)
| 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 |
| 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 |