AVITA Medical Reports Second Quarter Financial Results
Rhea-AI Summary
AVITA Medical (NASDAQ: RCEL) reported strong Q2 2024 financial results, with commercial revenue reaching $15.1 million, a 29% increase year-over-year. The company achieved a gross profit margin of 86.2%. Key highlights include FDA approval of RECELL GO™ and submission of a PMA supplement for RECELL GO mini™. AVITA entered an exclusive agreement with Regenity Biosciences for a collagen-based dermal matrix.
The company expects Q3 2024 commercial revenue between $19.0-$20.0 million and full-year 2024 revenue of $68.0-$70.0 million. AVITA anticipates achieving cashflow break-even and GAAP profitability by Q3 2025. Despite strong growth, the company reported a net loss of $15.4 million for Q2 2024, compared to $10.4 million in Q2 2023. As of June 30, 2024, AVITA had $54.1 million in cash and equivalents.
Positive
- Commercial revenue increased 29% year-over-year to $15.1 million
- Gross profit margin improved to 86.2%, up 500 bps from the previous year
- FDA approval of RECELL GO™ and submission of PMA supplement for RECELL GO mini™
- Exclusive agreement with Regenity Biosciences for collagen-based dermal matrix
- Projected Q3 2024 revenue growth of 40% to 48% year-over-year
- Full-year 2024 revenue guidance of $68.0 to $70.0 million, reflecting 37% to 41% growth
Negative
- Net loss increased to $15.4 million from $10.4 million in Q2 2023
- Operating expenses rose to $28.7 million from $21.2 million in Q2 2023
- BARDA income decreased to zero from $0.5 million in the previous year
- Interest expense increased by $1.3 million due to long-term debt
- Full-year revenue guidance adjusted downward
News Market Reaction 1 Alert
On the day this news was published, RCEL gained 20.68%, reflecting a significant positive market reaction.
Data tracked by StockTitan Argus on the day of publication.
VALENCIA, Calif., Aug. 08, 2024 (GLOBE NEWSWIRE) -- AVITA Medical, Inc. (NASDAQ: RCEL, ASX: AVH), a commercial-stage regenerative medicine company focused on first-in-class devices for wound care management and skin restoration, today reported financial results for the second quarter ended June 30, 2024.
Financial Results and Recent Business Updates
- Commercial revenue of
$15.1 million , an increase of approximately29% compared to the same period in 2023 - Gross profit margin of
86.2% - RECELL GO™ premarket approval (PMA) supplement approved by the FDA on May 29, 2024; first case completed on May 31, 2024
- Submitted PMA supplement for RECELL GO mini™, designed to address smaller wounds, on June 28, 2024; maintains Breakthrough Device designation ensuring a prioritized 180-day interactive review period
- Entered into an exclusive development and distribution agreement with Regenity Biosciences ("Regenity") providing AVITA Medical with the commercialization rights to a unique collagen-based dermal matrix following 510(k) clearance
“Our second-quarter commercial revenue reached a record
Future Milestones
- Expect Regenity to receive 510(k) clearance for the dermal matrix in the fourth quarter of 2024; following clearance, AVITA Medical will begin to market, sell, and distribute
- Plan to initiate multiple post-market clinical studies to establish the unique synergies between the new dermal matrix and RECELL
- Anticipate FDA approval of RECELL GO mini by December 27, 2024
- Expect to submit both our post-market study (TONE) treating patients with stable vitiligo and separate health care economics study for publication by year-end
Financial Guidance
- Commercial revenue for the third quarter 2024 is expected to be in the range of
$19.0 t o$20.0 million , reflecting growth of approximately40% to48% over the same period in 2023 - Commercial revenue for the full-year 2024 is now expected to be in the range of
$68.0 t o$70.0 million , reflecting growth of approximately37% to41% over the full-year 2023 - Expect to achieve previously given guidance of cashflow break even and GAAP profitability no later than the end of the third quarter of 2025
“We anticipate sequential third-quarter commercial revenue growth between
Second Quarter 2024 Financial Results
Total revenues increased by
Gross profit margin was
BARDA income decreased to zero, compared to
Total operating expenses for the quarter were
Interest expense increased approximately
Other income, net increased by
Net loss was
As of June 30, 2024, the Company had approximately
Webcast and Conference Call Information
AVITA Medical will host a conference call on Thursday, August 8, 2024 at 1:30 p.m. Pacific Time (Friday, August 9, 2024, at 6:30 a.m. Australian Eastern Standard Time) to discuss its financial results and recent business highlights. To participate by telephone, please register in advance to receive dial-in details and a personal PIN at https://register.vevent.com/register/BI460b032551fb410185009f5eac59ddac. The live webcast will be accessible through the Events section of AVITA Medical’s Investor Relations website at ir.avitamedical.com. A replay of the webcast will be available shortly after the live event.
About AVITA Medical, Inc.
AVITA Medical® is a commercial-stage regenerative medicine company transforming the standard of care in wound care management and skin restoration with innovative devices. At the forefront of our platform is the RECELL® System, approved by the Food and Drug Administration for the treatment of thermal burn wounds and full-thickness skin defects, and for repigmentation of stable depigmented vitiligo lesions. RECELL harnesses the regenerative properties of a patient’s own skin to create Spray-On Skin™ Cells, delivering a transformative solution at the point-of-care. This breakthrough technology serves as the catalyst for a new treatment paradigm enabling improved clinical outcomes. AVITA Medical also holds the exclusive rights to market, sell, and distribute PermeaDerm®, a biosynthetic wound matrix, in the United States.
In international markets, the RECELL System is approved to promote skin healing in a wide range of applications including burns, full-thickness skin defects, and vitiligo. The RECELL System is TGA-registered in Australia, has received CE-mark approval in Europe, and has PMDA approval in Japan.
To learn more, visit www.avitamedical.com.
CAUTIONARY NOTE REGARDING FORWARD-LOOKING STATEMENTS
This press release may contain forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Such forward-looking statements are subject to significant risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements. Forward-looking statements generally may 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,” and similar words or expressions, and the use of future dates. Forward-looking statements include, but are not limited to, statements relating to the timing and realization 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 outside of the Company’s control. These statements are made as of the date of this release, and the Company undertakes no obligation to publicly update or revise any of these statements, except as required by law. For additional information and other important factors that may cause actual results to differ materially from forward-looking statements, please see the “Risk Factors” section of the Company’s latest Annual Report on Form 10-K and other publicly available filings for a discussion of these and other risks and uncertainties.
Authorized for release by the Chief Financial Officer of AVITA Medical, Inc.
| AVITA MEDICAL, INC. Consolidated Balance Sheets (In thousands, except share and per share data) | ||||||||
| As of | ||||||||
| June 30, 2024 | December 31, 2023 | |||||||
| ASSETS | ||||||||
| Cash and cash equivalents | $ | 17,452 | $ | 22,118 | ||||
| Marketable securities | 36,604 | 66,939 | ||||||
| Accounts receivable, net | 8,717 | 7,664 | ||||||
| BARDA receivables | 94 | 30 | ||||||
| Prepaids and other current assets | 3,382 | 1,659 | ||||||
| Inventory | 6,709 | 5,596 | ||||||
| Total current assets | 72,958 | 104,006 | ||||||
| Plant and equipment, net | 7,024 | 1,877 | ||||||
| Operating lease right-of-use assets | 3,938 | 2,440 | ||||||
| Corporate-owned life insurance ("COLI") asset | 2,888 | 2,475 | ||||||
| Intangible assets, net | 545 | 487 | ||||||
| Other long-term assets | 473 | 355 | ||||||
| Total assets | $ | 87,826 | $ | 111,640 | ||||
| LIABILITIES, NON-QUALIFIED DEFERRED COMPENSATION PLAN SHARE AWARDS AND STOCKHOLDERS' EQUITY | ||||||||
| Accounts payable and accrued liabilities | 4,155 | 3,793 | ||||||
| Accrued wages and fringe benefits | 7,624 | 7,972 | ||||||
| Current non-qualified deferred compensation ("NQDC") liability | 753 | 168 | ||||||
| Other current liabilities | 1,255 | 1,266 | ||||||
| Total current liabilities | 13,787 | 13,199 | ||||||
| Long-term debt | 40,989 | 39,812 | ||||||
| Non-qualified deferred compensation liability | 3,148 | 3,663 | ||||||
| Contract liabilities | 340 | 357 | ||||||
| Operating lease liabilities, long term | 3,281 | 1,702 | ||||||
| Warrant liability | 1,968 | 3,158 | ||||||
| Total liabilities | 63,513 | 61,891 | ||||||
| Non-qualified deferred compensation plan share awards | 398 | 693 | ||||||
| Commitments and contingencies (Note 13) | ||||||||
| Stockholders' equity: | ||||||||
| Common stock, | 3 | 3 | ||||||
| Preferred stock, | - | - | ||||||
| Company common stock held by the non-qualified deferred compensation plan | (1,022 | ) | (1,130 | ) | ||||
| Additional paid-in capital | 358,510 | 350,039 | ||||||
| Accumulated other comprehensive loss | (1,556 | ) | (1,887 | ) | ||||
| Accumulated deficit | (332,020 | ) | (297,969 | ) | ||||
| Total stockholders' equity | 23,915 | 49,056 | ||||||
| Total liabilities, non-qualified deferred compensation plan share awards and stockholders' equity | $ | 87,826 | $ | 111,640 | ||||
| AVITA MEDICAL, INC. Consolidated Statements of Operations (In thousands, except share and per share data) (Unaudited) | ||||||||||||||||
| Three-Months Ended | Six-Months Ended | |||||||||||||||
| June 30, 2024 | June 30, 2023 | June 30, 2024 | June 30, 2023 | |||||||||||||
| Sales revenue | $ | 15,183 | $ | 11,753 | $ | 26,287 | $ | 22,303 | ||||||||
| Lease revenue | 12 | - | 12 | - | ||||||||||||
| Total revenues | 15,195 | 11,753 | 26,299 | 22,303 | ||||||||||||
| Cost of sales | (2,111 | ) | (2,204 | ) | (3,624 | ) | (3,871 | ) | ||||||||
| Gross profit | 13,084 | 9,549 | 22,675 | 18,432 | ||||||||||||
| BARDA income | - | 530 | - | 1,157 | ||||||||||||
| Operating expenses: | ||||||||||||||||
| Sales and marketing | (16,302 | ) | (10,003 | ) | (28,942 | ) | (16,543 | ) | ||||||||
| General and administrative | (7,519 | ) | (6,165 | ) | (16,481 | ) | (14,460 | ) | ||||||||
| Research and development | (4,887 | ) | (5,076 | ) | (10,081 | ) | (9,662 | ) | ||||||||
| Total operating expenses | (28,708 | ) | (21,244 | ) | (55,504 | ) | (40,665 | ) | ||||||||
| Operating loss | (15,624 | ) | (11,165 | ) | (32,829 | ) | (21,076 | ) | ||||||||
| Interest expense | (1,347 | ) | (7 | ) | (2,703 | ) | (11 | ) | ||||||||
| Other income, net | 1,611 | 801 | 1,544 | 1,526 | ||||||||||||
| Loss before income taxes | (15,360 | ) | (10,371 | ) | (33,988 | ) | (19,561 | ) | ||||||||
| Income tax expense | (33 | ) | (13 | ) | (63 | ) | (43 | ) | ||||||||
| Net loss | $ | (15,393 | ) | $ | (10,384 | ) | $ | (34,051 | ) | $ | (19,604 | ) | ||||
| Net loss per common share: | ||||||||||||||||
| Basic and diluted | $ | (0.60 | ) | $ | (0.41 | ) | $ | (1.32 | ) | $ | (0.78 | ) | ||||
| Weighted-average common shares: | ||||||||||||||||
| Basic and diluted | 25,760,278 | 25,239,723 | 25,699,030 | 25,221,009 | ||||||||||||