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UNITY Biotechnology, Inc. Reports Fourth Quarter and Full Year 2024 Financial Results and Business Updates

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UNITY Biotechnology (NASDAQ: UBX) has reported its Q4 and full-year 2024 financial results. The company anticipates receiving 24-week topline data from its Phase 2b ASPIRE study for UBX1325 (foselutoclax) in diabetic macular edema (DME) in Q1 2025, followed by 36-week data in Q2 2025.

Financial highlights include:

  • Cash position of $23.2 million as of December 31, 2024 (down from $43.2M in 2023)
  • Full-year 2024 net loss of $26.0 million (improved from $39.9M in 2023)
  • Q4 2024 net loss of $8.4 million (compared to $4.3M in Q4 2023)
  • Research and development expenses decreased to $13.0 million in 2024 (from $20.1M in 2023)
  • General and administrative expenses reduced to $15.5 million in 2024 (from $19.0M in 2023)

UNITY Biotechnology (NASDAQ: UBX) ha riportato i risultati finanziari del quarto trimestre e dell'intero anno 2024. L'azienda prevede di ricevere i dati preliminari a 24 settimane dal suo studio di Fase 2b ASPIRE per UBX1325 (foselutoclax) nel trattamento dell'edema maculare diabetico (DME) nel primo trimestre del 2025, seguiti dai dati a 36 settimane nel secondo trimestre del 2025.

I punti salienti finanziari includono:

  • Posizione di cassa di 23,2 milioni di dollari al 31 dicembre 2024 (in calo rispetto ai 43,2 milioni di dollari nel 2023)
  • Perdita netta dell'intero anno 2024 di 26,0 milioni di dollari (migliorata rispetto ai 39,9 milioni di dollari nel 2023)
  • Perdita netta del quarto trimestre 2024 di 8,4 milioni di dollari (rispetto ai 4,3 milioni di dollari nel Q4 2023)
  • Le spese per ricerca e sviluppo sono diminuite a 13,0 milioni di dollari nel 2024 (rispetto ai 20,1 milioni di dollari nel 2023)
  • Le spese generali e amministrative sono state ridotte a 15,5 milioni di dollari nel 2024 (rispetto ai 19,0 milioni di dollari nel 2023)

UNITY Biotechnology (NASDAQ: UBX) ha reportado sus resultados financieros del cuarto trimestre y del año completo 2024. La compañía anticipa recibir datos preliminares a 24 semanas de su estudio de Fase 2b ASPIRE para UBX1325 (foselutoclax) en el edema macular diabético (DME) en el primer trimestre de 2025, seguido de los datos a 36 semanas en el segundo trimestre de 2025.

Los aspectos financieros destacados incluyen:

  • Posición de efectivo de 23,2 millones de dólares al 31 de diciembre de 2024 (una disminución de 43,2 millones de dólares en 2023)
  • Pérdida neta del año completo 2024 de 26,0 millones de dólares (mejorada desde 39,9 millones de dólares en 2023)
  • Pérdida neta del cuarto trimestre 2024 de 8,4 millones de dólares (en comparación con 4,3 millones de dólares en el cuarto trimestre de 2023)
  • Los gastos de investigación y desarrollo se redujeron a 13,0 millones de dólares en 2024 (desde 20,1 millones de dólares en 2023)
  • Los gastos generales y administrativos se redujeron a 15,5 millones de dólares en 2024 (desde 19,0 millones de dólares en 2023)

유니티 생명과학(나스닥: UBX)은 2024년 4분기 및 전체 연도 재무 결과를 발표했습니다. 이 회사는 2025년 1분기에 당뇨병성 황반부종(DME) 치료를 위한 UBX1325(포셀루토클락스)의 2b상 ASPIRE 연구에서 24주 주요 데이터를 받을 것으로 예상하고 있으며, 2025년 2분기에는 36주 데이터를 받을 예정입니다.

재무 하이라이트는 다음과 같습니다:

  • 2024년 12월 31일 기준 현금 보유액 2320만 달러 (2023년 4320만 달러에서 감소)
  • 2024년 전체 연도 순손실 2600만 달러 (2023년 3990만 달러에서 개선됨)
  • 2024년 4분기 순손실 840만 달러 (2023년 4분기 430만 달러와 비교)
  • 2024년 연구개발비용이 1300만 달러로 감소 (2023년 2010만 달러에서)
  • 2024년 일반관리비용이 1550만 달러로 감소 (2023년 1900만 달러에서)

UNITY Biotechnology (NASDAQ: UBX) a annoncé ses résultats financiers pour le quatrième trimestre et l'année entière 2024. L'entreprise prévoit de recevoir des données préliminaires de 24 semaines de son étude de Phase 2b ASPIRE pour UBX1325 (foselutoclax) dans le traitement de l'œdème maculaire diabétique (DME) au premier trimestre 2025, suivies de données à 36 semaines au deuxième trimestre 2025.

Les points forts financiers comprennent :

  • Position de trésorerie de 23,2 millions de dollars au 31 décembre 2024 (en baisse par rapport à 43,2 millions de dollars en 2023)
  • Perte nette de l'année 2024 de 26,0 millions de dollars (améliorée par rapport à 39,9 millions de dollars en 2023)
  • Perte nette du quatrième trimestre 2024 de 8,4 millions de dollars (comparé à 4,3 millions de dollars au quatrième trimestre 2023)
  • Les dépenses de recherche et développement ont diminué à 13,0 millions de dollars en 2024 (contre 20,1 millions de dollars en 2023)
  • Les dépenses générales et administratives ont été réduites à 15,5 millions de dollars en 2024 (contre 19,0 millions de dollars en 2023)

UNITY Biotechnology (NASDAQ: UBX) hat seine Finanzberichte für das vierte Quartal und das Gesamtjahr 2024 veröffentlicht. Das Unternehmen erwartet, im ersten Quartal 2025 Daten aus seiner Phase-2b-Studie ASPIRE zu UBX1325 (Foselutoclax) zur Behandlung von diabetischem Makulaödem (DME) zu erhalten, gefolgt von Daten nach 36 Wochen im zweiten Quartal 2025.

Finanzielle Höhepunkte umfassen:

  • Liquiditätsposition von 23,2 Millionen Dollar zum 31. Dezember 2024 (ein Rückgang von 43,2 Millionen Dollar im Jahr 2023)
  • Jahresverlust 2024 von 26,0 Millionen Dollar (verbessert von 39,9 Millionen Dollar im Jahr 2023)
  • Quartalsverlust im vierten Quartal 2024 von 8,4 Millionen Dollar (im Vergleich zu 4,3 Millionen Dollar im vierten Quartal 2023)
  • Forschungs- und Entwicklungskosten sanken auf 13,0 Millionen Dollar im Jahr 2024 (von 20,1 Millionen Dollar im Jahr 2023)
  • Allgemeine und Verwaltungskosten wurden auf 15,5 Millionen Dollar im Jahr 2024 gesenkt (von 19,0 Millionen Dollar im Jahr 2023)
Positive
  • Net loss improved by 34.8% to $26.0M in 2024
  • R&D expenses reduced by 35.3% to $13.0M
  • G&A expenses decreased by 18.4% to $15.5M
  • Cash burn reduced: $20.9M used in 2024 vs $37.1M in 2023
Negative
  • Cash position declined 46.3% to $23.2M
  • Q4 net loss increased 95.3% to $8.4M
  • Significant workforce reduction implemented
  • Facility downsizing through sublease of East Grand facility

Insights

Unity Biotechnology's Q4 and FY2024 results reflect improved operational efficiency amid advancing clinical programs. The company reported a net loss of $26.0 million for 2024, a significant improvement from $39.9 million in 2023. Cash burn decreased to $20.9 million from $37.1 million year-over-year, demonstrating effective cost management.

The company's cash position stands at $23.2 million, providing runway into Q4 2025. This timeline is critical as it aligns with upcoming catalysts for UBX1325 (foselutoclax), their lead candidate for diabetic macular edema (DME). The Phase 2b ASPIRE study is approaching important milestones with 24-week primary endpoint data expected this quarter and 36-week data in Q2 2025.

The strategic focus on UBX1325 represents a targeted approach in addressing DME, a condition with significant unmet needs despite existing treatments. The senolytic mechanism of action differentiates UBX1325 from current anti-VEGF therapies, potentially offering improved durability and reduced treatment burden.

The reduction in R&D expenses by $7.1 million to $13.0 million reflects completion of earlier studies and streamlined operations. G&A expenses similarly decreased by $3.5 million to $15.5 million, largely due to headcount reductions and facility subleasing.

While the company has successfully reduced expenses, the upcoming clinical readouts will be decisive for Unity's future direction and potential partnership opportunities, making this a pivotal period for investors following the DME treatment landscape.

Unity Biotechnology has reported its financial results for Q4 and full year 2024, highlighting both fiscal discipline and clinical progress. The company has successfully reduced its annual net loss to $26.0 million from $39.9 million in 2023, with cash used in operations decreasing to $20.9 million from $37.1 million year-over-year. This improved efficiency stems from strategic reductions in both R&D and G&A expenses through headcount optimization and facility subleasing. The company's cash position of $23.2 million provides runway into Q4 2025, coinciding with critical upcoming milestones for their lead candidate UBX1325 (foselutoclax). They expect to report 24-week primary endpoint data from the Phase 2b ASPIRE study in diabetic macular edema (DME) this quarter, followed by 36-week data in Q2 2025. The ASPIRE study represents a direct head-to-head comparison against aflibercept, the current standard of care. UBX1325's novel senolytic mechanism potentially addresses key limitations of existing anti-VEGF therapies, particularly treatment burden and suboptimal response rates. Management believes this differentiated approach could provide meaningful advantages for DME patients who continue to experience vision loss despite current therapies. While the operational improvements are encouraging, Unity's future trajectory hinges significantly on these upcoming clinical readouts. The data will be instrumental in determining the design of potential pivotal trials and advancing their program toward commercialization. This makes the coming quarters particularly consequential for the company's long-term prospects in the ophthalmology space.

SAN FRANCISCO, March 07, 2025 (GLOBE NEWSWIRE) -- UNITY Biotechnology, Inc. (“UNITY”) [NASDAQ: UBX], a biotechnology company developing therapeutics to slow, halt, or reverse diseases of aging, today reported financial results for the fourth quarter and full year ended December 31, 2024.

“We expect to receive 24-week topline data from our Phase 2b ASPIRE study in diabetic macular edema (DME) in this quarter,” said Anirvan Ghosh, Ph.D., chief executive officer of UNITY. “DME remains a significant unmet need, and we believe UBX1325 (foselutoclax) has the potential to provide a differentiated treatment option for patients who continue to experience vision loss despite current standard-of-care therapies. With its novel mechanism of action and durable therapeutic profile, UBX1325 could offer meaningful advantages over existing anti-VEGF treatments. The 24-week data as well as the 36-week data will be instrumental in shaping our plans for a potential pivotal trial and advancing our program.”

UBX1325 (foselutoclax) is designed as a novel and durable therapeutic option in DME that acts via a senolytic mechanism of action, with the potential to address shortcomings of the current standard of care, such as high treatment burden and sub-optimal response to treatment.

UNITY anticipates receiving 24-week primary endpoint data in the first quarter of 2025 and 36-week data in the second quarter of 2025. The Phase 2b ASPIRE study in DME is a multi-center, randomized, double-masked, active-controlled study designed to evaluate the safety and efficacy of UBX1325 in a head-to-head comparison to aflibercept. More information about ASPIRE (NCT06011798) can be found here.

Fourth Quarter and Full Year Financial Results

Cash, cash equivalents and marketable securities totaled $23.2 million as of December 31, 2024 compared with $43.2 million as of December 31, 2023. UNITY believes that current cash, cash equivalents and marketable securities are sufficient to fund operations into the fourth quarter of 2025.

Net loss for the twelve months ended December 31, 2024 was $26.0 million compared to $39.9 million for the twelve months ended December 31, 2023. Cash used in operations during the year ended December 31, 2024 was $20.9 million compared to $37.1 million for the twelve months ended December 31, 2023. Total net loss for the fourth quarter of 2024 was $8.4 million compared to $4.3 million for the fourth quarter of 2023. Cash used in operations during the fourth quarter of 2024 was $5.9 million compared to $6.7 million for the fourth quarter of 2023.

Research and development expenses decreased by $7.1 million, to $13.0 million for the year ended December 31, 2024 from $20.1 million for the year ended December 31, 2023. The decrease was primarily due to decreases of $3.5 million in personnel costs due to our reduced headcount and the reduction in force, $2.7 million in direct research and development expenses mainly due to the completion of our UBX1325 BEHOLD and ENVISION studies, and $0.9 million in facilities-related costs primarily due to the sublease of our East Grand facility. Research and development expenses decreased by $0.2 million, to $3.1 million for the fourth quarter of 2024 from $3.3 million for the fourth quarter of 2023. The decrease was due to decreases of $0.5 million in personnel-related costs due to reduced headcount, partially offset by a increase of $0.3 million in direct research and development expenses primarily due to the ongoing UBX1325 ASPIRE study.

General and administrative expenses decreased by $3.5 million, to $15.5 million for the year ended December 31, 2024 from $19.0 million for the year ended December 31, 2023. The decrease was primarily due to decreases of $2.5 million in personnel costs due to our reduced headcount and reduction in force, $0.4 million in professional fees, and $0.6 million in facilities-related costs primarily due to the sublease of our East Grand facility. General and administrative expenses decreased by $0.1 million, to $4.3 million for the fourth quarter of 2024 from $4.4 million for the fourth quarter of 2023. The decrease was primarily due to decreases of $0.2 million in personnel-related costs due to lower headcount, partially offset by increases of $0.1 million in professional and consulting fees.

About UNITY
UNITY is developing a new class of therapeutics to slow, halt, or reverse diseases of aging. UNITY’s current focus is on creating medicines to selectively eliminate or modulate senescent cells and thereby provide transformative benefit in age-related ophthalmologic and neurologic diseases. More information is available at www.unitybiotechnology.com or follow us on X and LinkedIn.

Forward-Looking Statements
This press release contains forward-looking statements including statements related to UNITY’s understanding of cellular senescence and the role it plays in diseases of aging, the potential for UNITY to develop therapeutics to slow, halt, or reverse diseases of aging, including for ophthalmologic and neurologic diseases, the potential for UNITY to successfully commence and complete clinical studies of UBX1325 for DME, AMD, and other ophthalmologic diseases, the expected timing of enrollment and results of the clinical trials in UBX1325, and UNITY’s expectations regarding the sufficiency of its cash runway. These statements involve substantial known and unknown risks, uncertainties, and other factors that may cause our actual results, levels of activity, performance, or achievements to be materially different from the information expressed or implied by these forward-looking statements, including risks related to delay or disruption in the enrollment of patients in clinical trials, risks relating to the uncertainties inherent in the drug development process, and risks relating to UNITY’s understanding of senescence biology. We may not actually achieve the plans, intentions, or expectations disclosed in our forward-looking statements, and you should not place undue reliance on our forward-looking statements. Actual results or events could differ materially from the plans, intentions and expectations disclosed in the forward-looking statements we make. The forward-looking statements in this press release represent our views as of the date of this release. We anticipate that subsequent events and developments will cause our views to change. However, while we may elect to update these forward-looking statements at some point in the future, we have no current intention of doing so except to the extent required by applicable law. You should, therefore, not rely on these forward-looking statements as representing our views as of any date subsequent to the date of this release. For a further description of the risks and uncertainties that could cause actual results to differ from those expressed in these forward-looking statements, as well as risks relating to the business of the Company in general, see UNITY’s most recent Annual Report on Form 10-K for the year ended December 31, 2024, filed with the Securities and Exchange Commission on March 7, 2025, as well as other documents that may be filed by UNITY from time to time with the Securities and Exchange Commission.

  
Unity Biotechnology, Inc. 
Statements of Operations and Comprehensive Loss 
(In thousands, except share and per share amounts) 
  
  Three Months Ended  Year Ended 
  December 31,  December 31, 
  2024  2023  2024  2023 
  (Unaudited)       
Operating expenses:            
Research and development $3,035  $3,271  $13,006  $20,099 
General and administrative  4,251   4,406   15,460   18,966 
Impairment of long-lived assets  2,705      2,705   5,602 
Total operating expenses  9,991   7,677   31,171   44,667 
Loss from operations  (9,991)  (7,677)  (31,171)  (44,667)
Interest income  309   525   1,733   2,874 
Interest expense           (2,452)
Gain on warrant liability  1,306   3,932   3,713   6,215 
Other expense, net  (64)  (1,119)  (265)  (1,830)
Net loss  (8,440)  (4,339)  (25,990)  (39,860)
Other comprehensive gain (loss)            
Unrealized gain (loss) on marketable debt securities  (24)  31   39   227 
Comprehensive loss $(8,464) $(4,308) $(25,951) $(39,633)
Net loss per share, basic and diluted $(0.50) $(0.28) $(1.54) $(2.70)
Weighted-average number of shares used in computing net loss per share, basic and diluted  16,857,810   15,743,772   16,827,038   14,773,612 



Unity Biotechnology, Inc. 
Condensed Balance Sheets 
(In thousands) 
  
  December 31,  December 31, 
  2024  2023 
Assets      
Current Assets:      
Cash and cash equivalents $7,580  $19,803 
Short-term marketable securities  15,650   23,398 
Prepaid expenses and other current assets  1,037   3,404 
Total current assets  24,267   46,605 
Property and equipment, net  3,456   5,082 
Operating lease right-of-use assets  8,900   12,981 
Long-term restricted cash  896   896 
Other long-term assets  143   126 
Total assets $37,662  $65,690 
Liabilities and Stockholders’ Equity      
Current liabilities:      
Accounts payable $997  $1,380 
Accrued compensation  2,096   1,841 
Accrued and other current liabilities  6,167   4,619 
Total current liabilities  9,260   7,840 
Operating lease liability, net of current portion  19,709   23,539 
Warrant liability  2,199   5,913 
Total liabilities  31,168   37,292 
Commitments and contingencies      
Stockholders’ equity:      
Common stock  2   2 
Additional paid-in capital  516,820   512,773 
Accumulated other comprehensive gain  15   (24)
Accumulated deficit  (510,343)  (484,353)
Total stockholders’ equity  6,494   28,398 
Total liabilities and stockholders’ equity $37,662  $65,690 
 

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FAQ

When will UNITY Biotechnology (UBX) release the ASPIRE study results for UBX1325?

24-week topline data expected in Q1 2025, with 36-week data following in Q2 2025.

How much cash does UBX have and how long will it last?

$23.2M in cash as of December 31, 2024, sufficient to fund operations into Q4 2025.

What was UBX's net loss for full-year 2024?

$26.0 million, improved from $39.9 million in 2023.

How much did UBX reduce its R&D expenses in 2024?

R&D expenses decreased by $7.1M to $13.0M in 2024, down from $20.1M in 2023.

What is the potential advantage of UBX1325 over existing DME treatments?

UBX1325 offers a novel senolytic mechanism of action with potential for more durable treatment effects compared to current anti-VEGF therapies.
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