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AVITA Medical Reports Second Quarter Financial Results

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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.

AVITA Medical (NASDAQ: RCEL) ha riportato risultati finanziari solidi per il secondo trimestre del 2024, con entrate commerciali che hanno raggiunto i 15,1 milioni di dollari, un aumento del 29% rispetto all'anno precedente. L'azienda ha ottenuto un margine di profitto lordo del 86,2%. Tra i punti salienti c'è l'approvazione della FDA per RECELL GO™ e la presentazione di un supplemento PMA per RECELL GO mini™. AVITA ha stipulato un accordo esclusivo con Regenity Biosciences per una matrice dermica a base di collagene.

L'azienda prevede per il terzo trimestre del 2024 entrate commerciali tra i 19,0 e i 20,0 milioni di dollari e entrate totali per l'intero anno 2024 tra i 68,0 e i 70,0 milioni di dollari. AVITA anticipa di raggiungere il pareggio di flusso di cassa e la redditività GAAP entro il terzo trimestre del 2025. Nonostante una forte crescita, l'azienda ha riportato una perdita netta di 15,4 milioni di dollari per il secondo trimestre del 2024, rispetto ai 10,4 milioni di dollari nel secondo trimestre del 2023. Al 30 giugno 2024, AVITA aveva 54,1 milioni di dollari in contante e equivalenti.

AVITA Medical (NASDAQ: RCEL) reportó resultados financieros sólidos para el segundo trimestre de 2024, con ingresos comerciales que alcanzaron los 15,1 millones de dólares, un aumento del 29% interanual. La compañía logró un margen de ganancia bruta del 86,2%. Los puntos destacados incluyen la aprobación de la FDA para RECELL GO™ y la presentación de un suplemento PMA para RECELL GO mini™. AVITA firmó un acuerdo exclusivo con Regenity Biosciences para una matriz dérmica a base de colágeno.

La compañía espera que los ingresos comerciales del tercer trimestre de 2024 se sitúen entre 19,0 y 20,0 millones de dólares y los ingresos totales para todo el 2024 sean de entre 68,0 y 70,0 millones de dólares. AVITA anticipa alcanzar el equilibrio de flujo de caja y la rentabilidad GAAP para el tercer trimestre de 2025. A pesar de un fuerte crecimiento, la compañía reportó una pérdida neta de 15,4 millones de dólares para el segundo trimestre de 2024, en comparación con los 10,4 millones de dólares en el segundo trimestre de 2023. A 30 de junio de 2024, AVITA tenía 54,1 millones de dólares en efectivo y equivalentes.

AVITA Medical (NASDAQ: RCEL)는 2024년 2분기 강력한 재무 결과를 발표했으며, 상업 수익이 1,510만 달러에 도달하여 전년 대비 29% 증가했습니다. 회사는 총 매출 이익률이 86.2%에 달했습니다. 주요 하이라이트로는 RECELL GO™에 대한 FDA 승인과 RECELL GO mini™에 대한 PMA 보충 제출이 있습니다. AVITA는 Regenity Biosciences와 콜라겐 기반 피부 기질에 대한 독점 계약을 체결했습니다.

회사는 2024년 3분기 상업 수익이 1,900만에서 2,000만 달러에 이를 것으로 예상하며, 2024년 전체 수익은 6,800만에서 7,000만 달러에 이를 것으로 보입니다. AVITA는 2025년 3분기까지 현금 흐름 브레이크 이븐과 GAAP 수익성을 달성할 것으로 예상하고 있습니다. 강력한 성장에도 불구하고, 회사는 2024년 2분기에 1,540만 달러의 순 손실을 기록했으며, 이는 2023년 2분기의 1,040만 달러와 비교됩니다. 2024년 6월 30일 기준으로 AVITA는 5,410만 달러의 현금 및 현금성 자산을 보유하고 있었습니다.

AVITA Medical (NASDAQ: RCEL) a signalé des résultats financiers solides pour le deuxième trimestre 2024, avec des revenus commerciaux atteignant 15,1 millions de dollars, soit une augmentation de 29 % par rapport à l'année précédente. L'entreprise a réalisé un marge brute de 86,2%. Parmi les points forts, on note l'approbation de la FDA pour RECELL GO™ et la soumission d'un supplément PMA pour RECELL GO mini™. AVITA a conclu un accord exclusif avec Regenity Biosciences pour une matrice dermique à base de collagène.

L'entreprise prévoit pour le troisième trimestre 2024 des revenus commerciaux compris entre 19,0 et 20,0 millions de dollars et des revenus totaux pour l'année 2024 de 68,0 à 70,0 millions de dollars. AVITA anticipe d'atteindre l'équilibre en trésorerie et une rentabilité GAAP d'ici le troisième trimestre 2025. Malgré une forte croissance, l'entreprise a enregistré une perte nette de 15,4 millions de dollars pour le deuxième trimestre 2024, contre 10,4 millions de dollars pour le deuxième trimestre 2023. Au 30 juin 2024, AVITA disposait de 54,1 millions de dollars en liquidités et équivalents.

AVITA Medical (NASDAQ: RCEL) hat starke Finanzielle Ergebnisse für das 2. Quartal 2024 gemeldet, wobei die Umsatzerlöse 15,1 Millionen Dollar erreichten, was einem Anstieg von 29 % im Jahresvergleich entspricht. Das Unternehmen erzielte eine Bruttogewinnmarge von 86,2%. Zu den wichtigsten Highlights gehören die FDA-Zulassung für RECELL GO™ und die Einreichung eines PMA-Supplements für RECELL GO mini™. AVITA ging eine exklusive Vereinbarung mit Regenity Biosciences für eine kollagenbasierte Dermalmatrix ein.

Das Unternehmen erwartet für das 3. Quartal 2024 Umsatzerlöse zwischen 19,0 und 20,0 Millionen Dollar und einen Gesamtumsatz für das Jahr 2024 von 68,0 bis 70,0 Millionen Dollar. AVITA rechnet damit, bis zum 3. Quartal 2025 den Cashflow-Break-Even und die GAAP-Rentabilität zu erreichen. Trotz des starken Wachstums meldete das Unternehmen einen Nettoverlust von 15,4 Millionen Dollar im 2. Quartal 2024, verglichen mit 10,4 Millionen Dollar im 2. Quartal 2023. Zum 30. Juni 2024 hatte AVITA 54,1 Millionen Dollar in Bargeld und Äquivalenten.

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

AVITA Medical's Q2 results show strong commercial momentum with revenue growth of 29% year-over-year to $15.1 million. The gross profit margin improved significantly to 86.2%, up 500 basis points from last year. However, the company's net loss widened to $15.4 million due to increased operating expenses, primarily in sales and marketing.

The company's guidance for Q3 revenue of $19.0-$20.0 million implies continued strong growth. However, the full-year revenue guidance was adjusted downward, though still projecting 37-41% growth. AVITA expects to achieve cashflow break-even and GAAP profitability by Q3 2025, which is positive for long-term sustainability.

With $54.1 million in cash and equivalents, AVITA has a decent runway to support its growth initiatives. Investors should monitor the balance between revenue growth and increasing expenses, as well as progress towards profitability.

AVITA's recent regulatory achievements are significant for its growth strategy. The FDA approval of RECELL GO™ and the submission of a PMA supplement for RECELL GO mini™ with Breakthrough Device designation demonstrate the company's commitment to expanding its wound care portfolio. These advancements could potentially broaden AVITA's addressable market and strengthen its competitive position.

The exclusive agreement with Regenity Biosciences for a collagen-based dermal matrix is a strategic move to diversify AVITA's product offerings. This complementary product could create synergies with RECELL, potentially enhancing treatment outcomes and driving adoption. The planned post-market studies will be important in establishing clinical evidence for these synergies.

AVITA's focus on becoming a broad-based wound care company is promising, but execution and market adoption of new products will be key to long-term success. Investors should watch for the 510(k) clearance of the dermal matrix and the approval of RECELL GO mini™ as important catalysts.

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 approximately 29% 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 $15.1 million, reflecting the effectiveness of our enhanced focus on commercial execution,” said Jim Corbett, Chief Executive Officer of AVITA Medical. “The FDA approval of RECELL GO and our recent submission of RECELL GO mini highlight our progress in expanding treatment capabilities for burn and full-thickness skin defects. Additionally, our agreement with Regenity further enhances our ability to address a full spectrum of clinical needs. We remain committed to establishing RECELL as the standard of care for wound therapy while continuing to transform AVITA Medical into a broad-based wound care company, ultimately improving accessibility and reaching more patients.”

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 to $20.0 million, reflecting growth of approximately 40% to 48% over the same period in 2023
  • Commercial revenue for the full-year 2024 is now expected to be in the range of $68.0 to $70.0 million, reflecting growth of approximately 37% to 41% 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 26% to 32% over the second quarter,” said David O'Toole, Chief Financial Officer of AVITA Medical. “Following our solid second quarter and a strong start in July, we are confident in our commercial team's ability to achieve this goal. However, we have adjusted downward our full-year revenue guidance, which still reflects a growth rate of over 37% year-over-year and our ongoing growth trajectory. With positive new developments, including the launch of RECELL GO and PermeaDerm, as well as the anticipated launch of our new dermal matrix, we intend to build on our second-quarter momentum and continue delivering strong results.”

Second Quarter 2024 Financial Results

Total revenues increased by 29.3%, or $3.4 million, to $15.2 million, compared to $11.8 million in the same period in the prior year. Our commercial revenue was $15.1 million in the three-months ended June 30, 2024, an increase of $3.4 million, or 29.5%, compared to $11.7 million in the corresponding period in the prior year. The growth in commercial revenues was largely driven by deeper penetration within existing customer accounts and new accounts for full-thickness skin defect.

Gross profit margin was 86.2% compared to 81.2%, representing an increase of 500 bps from the corresponding period in the prior year. This was largely driven by increases in revenues and the volume of production.

BARDA income decreased to zero, compared to $0.5 million in the corresponding period in the prior year due to the ending of reimbursable clinical trials. BARDA income in the prior year consisted of funding from the Biomedical Advanced Research and Development Authority, under the Assistant Secretary for Preparedness and Response, within the U.S. Department of Health and Human Services, under ongoing USG Contract No. HHSO100201500028C.

Total operating expenses for the quarter were $28.7 million, compared to $21.2 million in the same period in 2023. The increase in operating expenses is primarily attributable to an increase of $6.3 million in sales and marketing expenses due to employee-related costs, including salaries and benefits, commissions, professional fees, and travel expenses, collectively, as a result of the expansion of our commercial organization to support our growing commercial operations in the second quarter of 2023 and again in first quarter of 2024. G&A expenses increased by $1.4 million as a result of higher salaries and benefits, severance benefits, partially offset by lower deferred compensation expenses and lower professional fees. In addition, operating expenses were offset by a decrease of $0.2 million in R&D costs, which was primarily due to a decrease in professional fees and development expenses.

Interest expense increased approximately $1.3 million in comparison to the same period in the prior year due to the interest expense related to the long-term debt incurred as part of the OrbiMed Credit Agreement, for a principal amount owed of $40.0 million.

Other income, net increased by $0.8 million to income of $1.6 million. In the current period other income consists of income of $2.1 million related to the change in fair value of warrant liability, $0.7 million in income related to our investments. Income was offset by a non-cash charge of $1.2 million due to the change in fair value of the debt. The prior period income consisted of $0.7 million related to our investments and $0.1 million in gains.

Net loss was $15.4 million, or a loss of $0.60 per basic and diluted share, compared to a net loss of 10.4 million, or a loss of $0.41 per basic and diluted share, in the same period in 2023.

As of June 30, 2024, the Company had approximately $54.1 million in cash, cash equivalents, and marketable securities.

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, $0.0001 par value per share, 200,000,000 shares authorized, 25,949,906 and 25,682,078, shares issued and outstanding at June 30, 2024 and December 31, 2023, respectively  3   3 
Preferred stock, $0.0001 par value per share, 10,000,000 shares authorized, no shares issued or outstanding at June 30, 2024 and December 31, 2023  -   - 
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 

FAQ

What was AVITA Medical's (RCEL) commercial revenue for Q2 2024?

AVITA Medical's commercial revenue for Q2 2024 was $15.1 million, representing a 29% increase compared to the same period in 2023.

When did AVITA Medical (RCEL) receive FDA approval for RECELL GO™?

AVITA Medical received FDA approval for RECELL GO™ on May 29, 2024, with the first case completed on May 31, 2024.

What is AVITA Medical's (RCEL) revenue guidance for Q3 2024?

AVITA Medical expects Q3 2024 commercial revenue to be in the range of $19.0 to $20.0 million, reflecting growth of approximately 40% to 48% over the same period in 2023.

When does AVITA Medical (RCEL) expect to achieve cashflow break-even and GAAP profitability?

AVITA Medical expects to achieve cashflow break-even and GAAP profitability no later than the end of the third quarter of 2025.

What was AVITA Medical's (RCEL) gross profit margin in Q2 2024?

AVITA Medical's gross profit margin in Q2 2024 was 86.2%, an increase of 500 basis points from the corresponding period in the prior year.

Avita Medical, Inc.

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