Vir Biotechnology Reports Third Quarter 2024 Financial Results and Provides Corporate Update
Vir Biotechnology reported Q3 2024 financial results, highlighting a transformational quarter marked by the closing of an exclusive worldwide licensing agreement with Sanofi for three clinical-stage dual-masked T-cell engagers. The company reported a net loss of $(213.7) million, or $(1.56) per share. Total revenues were $2.4 million, with cash and investments of $1.19 billion. Key developments include promising Phase 2 SOLSTICE data in chronic hepatitis delta, appointment of Jason O'Byrne as CFO, and a strategic restructuring reducing workforce by 25%. The company updated its GAAP operating expense guidance to $660-680 million for 2024.
Vir Biotechnology ha riportato i risultati finanziari del terzo trimestre 2024, evidenziando un trimestre trasformativo contrassegnato dalla chiusura di un accordo di licenza esclusivo mondiale con Sanofi per tre attivatori T-cell dual-masked in fase clinica. L'azienda ha segnalato una perdita netta di $(213,7) milioni, ovvero $(1,56) per azione. Le entrate totali sono state di $2,4 milioni, con liquidità e investimenti di $1,19 miliardi. Sviluppi chiave includono dati promettenti della Fase 2 SOLSTICE sulla epatite delta cronica, nomina di Jason O'Byrne come CFO e una ristrutturazione strategica che riduce la forza lavoro del 25%. L'azienda ha aggiornato la sua guida delle spese operative GAAP a $660-680 milioni per il 2024.
Vir Biotechnology informó los resultados financieros del tercer trimestre de 2024, destacando un trimestre transformador marcado por el cierre de un acuerdo de licencia exclusivo mundial con Sanofi para tres engajadores de células T enmascarados duales en etapa clínica. La compañía reportó una pérdida neta de $(213,7) millones, o $(1,56) por acción. Los ingresos totales fueron de $2,4 millones, con efectivo e inversiones de $1,19 mil millones. Desarrollos clave incluyen datos prometedores de la Fase 2 SOLSTICE en hepatitis delta crónica, el nombramiento de Jason O'Byrne como CFO y una reestructuración estratégica que reduce la fuerza laboral en un 25%. La compañía actualizó su guía de gastos operativos GAAP a $660-680 millones para 2024.
Vir Biotechnology는 2024년 3분기 재무 결과를 발표하며, 삼중 위상 이중 마스크 T세포 조절제를 위한 Sanofi와의 독점 전 세계 라이센스 계약 체결로 특징지어진 변혁의 분기를 강조했습니다. 회사는 $(213.7)백만 또는 주당 $(1.56)의 순손실을 보고했습니다. 총 수입은 $2.4백만, 현금 및 투자금은 $1.19십억이었습니다. 주요 개발로는 만성 델타 간염에 대한 유망한 2상 SOLSTICE 데이터, Jason O'Byrne의 CFO 임명 및 25%의 인력 감소를 포함하는 전략적 구조조정이 있습니다. 회사는 2024년 GAAP 운영비 지침을 $660-680백만으로 업데이트했습니다.
Vir Biotechnology a annoncé les résultats financiers du troisième trimestre 2024, mettant en avant un trimestre transformateur marqué par la conclusion d'un accord de licence exclusif mondial avec Sanofi pour trois engageurs de cellules T masqués à double phase clinique. L'entreprise a signalé une perte nette de $(213,7) millions, soit $(1,56) par action. Les revenus totaux ont atteint $2,4 millions, avec des liquidités et des investissements de $1,19 milliard. DÉveloppements clés comprennent des données prometteuses de la phase 2 SOLSTICE sur l'hépatite delta chronique, la nomination de Jason O'Byrne en tant que CFO et une restructuration stratégique réduisant la main-d'œuvre de 25%. L'entreprise a mis à jour ses prévisions de dépenses d'exploitation en normes GAAP à $660-680 millions pour 2024.
Vir Biotechnology berichtete über die Finanzergebnisse des dritten Quartals 2024 und hob ein transformierendes Quartal hervor, das durch den Abschluss eines exklusiven weltweiten Lizenzvertrags mit Sanofi für drei klinisch getestete dual-maskierte T-Zell-Aktivatoren geprägt war. Das Unternehmen meldete einen Nettoverlust von $(213,7) Millionen, oder $(1,56) pro Aktie. Die Gesamteinnahmen betrugen $2,4 Millionen, mit Barmitteln und Investitionen von $1,19 Milliarden. Wichtige Entwicklungen umfassen vielversprechende Daten der Phase 2 SOLSTICE zu chronischer Delta-Hepatitis, die Ernennung von Jason O'Byrne zum CFO und eine strategische Umstrukturierung, die die Belegschaft um 25% reduziert. Das Unternehmen aktualisierte seine GAAP-Betriebsausgabenprognose auf $660-680 Millionen für 2024.
- Successful closing of exclusive worldwide licensing agreement with Sanofi for three potential best-in-class T-cell engagers
- Strong cash position of $1.19 billion as of September 30, 2024
- Promising Phase 2 SOLSTICE data showing high rates of virologic response in hepatitis delta treatment
- Fast Track Designation granted by FDA for tobevibart and elebsiran combination
- Net loss increased to $(213.7) million compared to $(163.4) million in Q3 2023
- Revenue declined to $2.4 million from $2.6 million year-over-year
- Workforce reduction of approximately 25% (140 employees)
- Cash decrease of $245.1 million during Q3 2024
Insights
The Q3 results show significant financial developments with a
The pipeline transformation marks a strategic shift with three dual-masked T-cell engagers acquired from Sanofi. Key catalysts include Phase 2 SOLSTICE data for chronic hepatitis delta and initial clinical data for VIR-5818 and VIR-5500 in Q1 2025. The hepatitis programs show promise, with Fast Track Designation for the tobevibart/elebsiran combination. The company's focus on high-value therapeutic areas while discontinuing COVID-19 and influenza programs demonstrates a refined strategy targeting areas with significant unmet needs.
– Successful closing of exclusive worldwide licensing agreement with Sanofi for three potential best-in-class clinical-stage dual-masked T-cell engagers with initial clinical data anticipated in Q1 2025 –
– Key Phase 2 SOLSTICE data in chronic hepatitis delta to be presented at AASLD 2024 –
– The Company will host a Hepatitis Investor Event following AASLD on November 19, 2024 –
– Jason O’Byrne appointed as Chief Financial Officer –
– Conference call scheduled for October 31, 2024 at 1:30 p.m. PT / 4:30 p.m. ET –
“This quarter was transformational for Vir. We have bolstered our clinical pipeline with three potential best-in-class dual-masked T-cell engagers in oncology, and have sharpened our focus within infectious diseases to the areas where we believe we can make the most significant impact for patients. We are also thrilled to welcome Jason O’Byrne as our new CFO. Jason brings a wealth of financial leadership experience, further strengthening our ability to bring these potentially transformative therapies to patients as quickly as possible,” said Marianne De Backer, M.Sc., Ph.D., MBA, Chief Executive Officer, Vir Biotechnology. “Looking ahead, this is an exciting time for the Company. We eagerly anticipate critical data in our hepatitis programs in the fourth quarter and look forward to sharing initial clinical data from our dual-masked T-cell engagers in the first quarter of 2025.”
Pipeline Programs
Chronic Hepatitis Delta (CHD)
- Preliminary data from the Phase 2 chronic hepatitis delta SOLSTICE study was presented at the European Study of the Liver (EASL) Meeting in June 2024. This data demonstrated the potential for transformative treatment for people living with chronic hepatitis delta, with both tobevibart as a monotherapy, and in combination with elebsiran, achieving high rates of virologic response and ALT normalization after 12 and 24 weeks of treatment. No treatment-related serious adverse events were observed.
-
The combination of tobevibart and elebsiran has been granted Fast Track Designation by the
U.S. FDA. Given the robust rates of virologic suppression observed with the combination, the Company is diligently working to advance this regimen into a pivotal development program as quickly as possible to address the urgent needs of these patients. -
At the upcoming American Association for the Study of Liver Diseases (AASLD) “The Liver Meeting” in November 2024, the Company will present additional data from the Phase 2 chronic hepatitis delta SOLSTICE trial, including: 24-week clinical data for both study cohorts in approximately 60 patients and further data for those patients who were on study beyond 24 weeks at the time of data cut-off.
- One cohort assesses the combination of tobevibart and elebsiran administered every four weeks, while a second cohort evaluates tobevibart monotherapy administered every two weeks.
- The SOLSTICE trial is evaluating the safety, tolerability and efficacy of tobevibart and elebsiran for the treatment of chronic hepatitis delta.
Chronic Hepatitis B (CHB)
-
The Company plans to share end-of-treatment data from the Phase 2 MARCH Part B trial as a Late Breaking presentation at the AASLD meeting in November 2024.
- The MARCH-B trial is evaluating the safety, tolerability and antiviral activity of the triplet combination of tobevibart and elebsiran plus peginterferon alfa-2a in approximately 30 participants, and approximately 50 participants treated with the doublet combination of tobevibart and elebsiran.
- The Company plans to share further data assessing a potential functional cure in the second quarter of 2025.
Solid Tumors
-
VIR-5818 is a dual-masked HER2-targeted T-cell engager in clinical development designed to minimize off-tumor toxicity, potentially allowing for higher doses and increased efficacy to address the significant unmet needs of patients with HER2 expressing cancers.
- A Phase 1 basket study of VIR-5818 as a monotherapy, and in combination with pembrolizumab, is on-going in multiple tumor types, including metastatic breast cancer and metastatic colorectal cancer.
- The Company plans to share initial clinical data for VIR-5818 in the first quarter of 2025.
-
VIR-5500 is a dual-masked PSMA directed T-cell engager in clinical development designed to minimize off-tumor toxicity and potentially improve efficacy relative to the existing approved PSMA-targeted therapies.
- A Phase 1 dose escalation study of VIR-5500 is ongoing to assess its safety profile and optimal dose levels for future development in metastatic-castration resistant prostate cancer.
- The Company plans to share initial clinical data for VIR-5500 in the first quarter of 2025.
-
VIR-5525 is a dual-masked EGFR targeted T-cell engager with a cleared Investigational New Drug Application (IND) from the
U.S. FDA.- The Company plans to initiate a Phase 1 basket study of VIR-5525 in the first quarter of 2025 in patients across a number of solid tumor indications of high unmet need, which may include metastatic head and neck squamous cell carcinoma, metastatic adenocarcinoma, squamous non-small cell lung cancer, and metastatic colorectal cancer.
Preclinical Pipeline Candidates
- The Company continues to advance pre-clinical assets in respiratory syncytial virus in partnership with GSK and pursue HIV cure in collaboration with the Bill & Melinda Gates Foundation.
Corporate Update
-
On August 1, 2024 the Company announced an exclusive worldwide license to three clinical-stage masked T-cell engagers (TCEs) with potential applications in a range of cancers, as well as the exclusive use of the proprietary PRO-XTEN™ masking platform for oncology and infectious disease. The Company announced closing of the agreement with Sanofi on September 9, 2024.
- Key employees from Sanofi, possessing extensive scientific and development expertise in TCEs, and in-depth experience with the PRO-XTEN™ platform, joined the Company following the closing of the agreement.
-
On August 1, 2024 the Company announced the phase-out of clinical programs in influenza, COVID-19, and its T-cell based viral vector platform. The Company is seeking partners to advance these clinical programs through further development. Additionally, the Company announced a workforce reduction of approximately
25% , or approximately 140 employees, and expects to end 2024 with approximately 435 employees – a decrease of approximately 200 from its peak headcount in the second quarter of 2023. - On September 10, 2024, the Company announced the appointment of Jason O’Byrne as Executive Vice President and Chief Financial Officer, effective October 2, 2024. Mr. O’Byrne is an accomplished executive with more than 20 years of finance and operations experience, and brings leadership in capital allocation and formation, corporate strategy and operational excellence.
- The Company will host two virtual investor events instead of the previously scheduled R&D Day in the fourth quarter of 2024. The first event, focusing on our hepatitis programs, will be held in November 2024, following the AASLD conference, and will provide detailed updates on our hepatitis delta and hepatitis B programs. In the first quarter of 2025, the Company will share initial clinical data for our masked T-cell engager programs during a second dedicated investor event.
Third Quarter 2024 Financial Results
Cash, Cash Equivalents and Investments: As of September 30, 2024, the Company had approximately
Revenues: Total revenues for the quarter ended September 30, 2024, were
Cost of Revenue: Cost of revenue was nominal for the third quarter of 2024 and 2023.
Research and Development Expenses (R&D): R&D expenses for the third quarter of 2024 were
Selling, General and Administrative Expenses (SG&A): SG&A expenses for the third quarter of 2024 were
Restructuring, long-lived assets impairment and related charges: Restructuring, long-lived assets impairment and related charges for the third quarter of 2024 were
Other Income: Other income for the third quarter of 2024 was
(Provision for) Benefit from Income Taxes: Provision for income taxes for the third quarter of 2024 was
Net Loss: Net loss attributable to Vir for the third quarter of 2024 was
2024 Financial Guidance
The Company has updated its operating expense guidance for the full-year 2024, which includes the upfront in-process research and development expense associated with the clinical-stage T-cell engagers licensed through its agreement with Sanofi:
(in $ millions) |
||||||
GAAP operating expense range: |
$ |
660 |
to |
$ |
680 |
|
The following expenses are included in the GAAP operating expense range: |
|
|
|
|||
Upfront payment to Sanofi recognized as R&D expense in the third quarter of 2024 |
|
|||||
Stock-based compensation expense |
$ |
90 |
to |
$ |
80 |
|
Restructuring charges* |
$ |
40 |
to |
$ |
30 |
|
* Restructuring charges include employee severance cash payouts, as well as non-cash expense related to the closing of two R&D sites previously announced on December 13, 2023. |
||||||
The GAAP operating expense guidance does not include the effect of GAAP adjustments caused by events that may occur subsequent to the publication of this guidance, including, but not limited to, business development activities, litigation, in-process R&D impairments, and changes in the fair value of contingent considerations.
Conference Call
Vir will host a conference call to discuss the third quarter results at 1:30 p.m. PT / 4:30 p.m. ET today. A live webcast will be available on https://investors.vir.bio/ and will be archived on www.vir.bio for 30 days.
About Tobevibart (VIR-3434)
Tobevibart is an investigational broadly neutralizing monoclonal antibody targeting the hepatitis B surface antigen. It is designed to inhibit the entry of hepatitis B and hepatitis delta viruses into hepatocytes, and to reduce the level of circulating viral and subviral particles in the blood. Tobevibart, which incorporates Xencor’s Xtend™ and other Fc technologies, has been engineered to have an extended half-life and was identified using Vir’s proprietary monoclonal antibody discovery platform. Tobevibart is administered subcutaneously, and it is currently in clinical development for treatment of patients with chronic hepatitis B and patients with chronic hepatitis delta.
About Elebsiran (VIR-2218)
Elebsiran is an investigational hepatitis B virus-targeting small interfering ribonucleic acid (siRNA) designed to degrade hepatitis B virus RNA transcripts and limit the production of hepatitis B surface antigen. Current data indicates that it has the potential to have direct antiviral activity against hepatitis B virus and hepatitis delta virus. Elebsiran is administered subcutaneously, and it is currently in clinical development for treatment of patients with chronic hepatitis B and patients with chronic hepatitis delta. It is the first asset in Vir’s collaboration with Alnylam Pharmaceuticals, Inc. to enter clinical studies.
About VIR-5818, VIR-5500, VIR-5525
VIR-5818, VIR-5500, VIR-5525 are investigational, clinical candidates currently being evaluated for the treatment of solid tumors. These assets leverage the PRO-XTEN™ masking technology with three different T-cell engagers (TCEs) targeting HER2, PSMA, and EGFR, respectively.
TCEs are powerful anti-tumor agents that direct the immune system, specifically T-cells, to destroy cancer cells. The PRO-XTEN™ masking technology is designed to keep the TCEs inactive (or masked) until they reach the tumor microenvironment, where tumor-specific proteases cleave off the mask and activate the TCEs leading to killing of cancer cells. By driving the activity exclusively to the tumor microenvironment, we aim to circumvent the traditionally high toxicity associated with TCEs and increase their efficacy and tolerability. Additionally, the mask also helps drug candidates stay in the bloodstream longer in their inactive form, allowing them to better reach the site of action and potentially allowing more convenient dosing regimens for patients and clinicians.
About Vir Biotechnology, Inc.
Vir Biotechnology, Inc. is a clinical-stage biopharmaceutical company focused on powering the immune system to transform lives by discovering and developing medicines for serious infectious diseases and cancer. Vir’s clinical-stage portfolio includes infectious disease programs for chronic hepatitis delta and chronic hepatitis B infections, in addition to programs across several clinically validated targets in solid tumor indications. Vir also has a preclinical portfolio of programs across a range of other infectious diseases and oncologic malignancies. Vir routinely posts information that may be important to investors on its website.
Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Words such as “should,” “could,” “may,” “might,” “will,” “plan,” “potential,” “aim,” “expect,” “anticipate,” “promising” and similar expressions (as well as other words or expressions referencing future events, conditions or circumstances) are intended to identify forward-looking statements. These forward-looking statements are based on Vir’s expectations and assumptions as of the date of this press release. Forward-looking statements contained in this press release include, but are not limited to, statements regarding; Vir’s cash balance; Vir’s future financial and operating results and its expectations related thereto including Vir’s financial guidance; Vir’s ability to realize the anticipated benefits from the exclusive worldwide license agreement with Sanofi; potential of, and expectations for, Vir’s pipeline; Vir’s clinical and preclinical development programs; clinical studies, including the enrollment of clinical studies, and the expected timing of data readouts and presentations; the potential benefits, safety, and efficacy of Vir’s investigational therapies; Vir’s strategy and plans; and risks and uncertainties associated with drug development and commercialization. Many factors may cause differences between current expectations and actual results, including whether or when anticipated cost reductions will be achieved; unexpected safety or efficacy data or results observed during clinical studies or in data readouts; the occurrence of adverse safety events; risks of unexpected costs, delays or other unexpected hurdles; difficulties in collaborating with other companies; successful development and/or commercialization of alternative product candidates by Vir’s competitors; changes in expected or existing competition; delays in or disruptions to Vir’s business or clinical studies due to geopolitical changes or other external factors; failure to achieve any necessary regulatory approvals; the timing and amount of actual expenses, including, without limitation, Vir’s anticipated combined GAAP R&D and SG&A expenses; and unexpected litigation or other disputes. Drug development and commercialization involve a high degree of risk, and only a small number of research and development programs result in commercialization of a product. Results in early-stage clinical studies may not be indicative of full results or results from later stage or larger scale clinical studies and do not ensure regulatory approval. You should not place undue reliance on these statements, or the scientific data presented. Other factors that may cause actual results to differ from those expressed or implied in the forward-looking statements in this press release are discussed in Vir’s filings with the
PRO-XTEN™ is a trademark of Amunix Pharmaceuticals, Inc., a Sanofi company.
VIR BIOTECHNOLOGY, INC. Condensed Consolidated Balance Sheets (in thousands, except share and per share data) (unaudited) |
|||||||
|
September 30,
|
|
December 31,
|
||||
ASSETS |
|
|
|
||||
CURRENT ASSETS: |
|
|
|
||||
Cash and cash equivalents |
$ |
168,350 |
|
|
$ |
241,576 |
|
Short-term investments |
|
740,607 |
|
|
|
1,270,980 |
|
Restricted cash and cash equivalents, current |
|
89,598 |
|
|
|
13,268 |
|
Equity investments |
|
5,517 |
|
|
|
9,853 |
|
Prepaid expenses and other current assets |
|
43,085 |
|
|
|
52,549 |
|
Total current assets |
|
1,047,157 |
|
|
|
1,588,226 |
|
Intangible assets, net |
|
19,258 |
|
|
|
22,565 |
|
Goodwill |
|
16,938 |
|
|
|
16,937 |
|
Property and equipment, net |
|
64,791 |
|
|
|
96,018 |
|
Operating lease right-of-use assets |
|
60,779 |
|
|
|
71,182 |
|
Restricted cash and cash equivalents, noncurrent |
|
6,382 |
|
|
|
6,448 |
|
Long-term investments |
|
271,495 |
|
|
|
105,275 |
|
Other assets |
|
11,556 |
|
|
|
12,409 |
|
TOTAL ASSETS |
$ |
1,498,356 |
|
|
$ |
1,919,060 |
|
LIABILITIES AND STOCKHOLDERS’ EQUITY |
|
|
|
||||
CURRENT LIABILITIES: |
|
|
|
||||
Accounts payable |
$ |
7,305 |
|
|
$ |
6,334 |
|
Accrued and other liabilities |
|
94,658 |
|
|
|
104,220 |
|
Deferred revenue, current |
|
15,198 |
|
|
|
64,853 |
|
Total current liabilities |
|
117,161 |
|
|
|
175,407 |
|
Operating lease liabilities, noncurrent |
|
93,405 |
|
|
|
111,673 |
|
Contingent consideration, noncurrent |
|
33,170 |
|
|
|
25,960 |
|
Other long-term liabilities |
|
13,893 |
|
|
|
15,784 |
|
TOTAL LIABILITIES |
|
257,629 |
|
|
|
328,824 |
|
Commitments and contingencies (Note 8) |
|
|
|
||||
STOCKHOLDERS’ EQUITY: |
|
|
|
||||
Preferred stock, |
|
— |
|
|
|
— |
|
Common stock, |
|
14 |
|
|
|
13 |
|
Additional paid-in capital |
|
1,894,781 |
|
|
|
1,828,862 |
|
Accumulated other comprehensive gain (loss) |
|
1,127 |
|
|
|
(815 |
) |
Accumulated deficit |
|
(655,195 |
) |
|
|
(237,824 |
) |
TOTAL STOCKHOLDERS’ EQUITY |
|
1,240,727 |
|
|
|
1,590,236 |
|
TOTAL LIABILITIES AND STOCKHOLDERS’ EQUITY |
$ |
1,498,356 |
|
|
$ |
1,919,060 |
|
VIR BIOTECHNOLOGY, INC. Condensed Consolidated Statements of Operations (in thousands, except share and per share data) (unaudited) |
|||||||
|
Three Months Ended
|
||||||
|
|
2024 |
|
|
|
2023 |
|
Revenues: |
|
|
|
||||
Collaboration revenue |
$ |
(1,102 |
) |
|
$ |
(4,387 |
) |
Contract revenue |
|
1,391 |
|
|
|
289 |
|
Grant revenue |
|
2,091 |
|
|
|
6,737 |
|
Total revenues |
|
2,380 |
|
|
|
2,639 |
|
Operating expenses: |
|
|
|
||||
Cost of revenue |
|
50 |
|
|
|
38 |
|
Research and development |
|
195,178 |
|
|
|
145,028 |
|
Selling, general and administrative |
|
25,744 |
|
|
|
40,933 |
|
Restructuring, long-lived assets impairment and related charges |
|
12,712 |
|
|
|
3,372 |
|
Total operating expenses |
|
233,684 |
|
|
|
189,371 |
|
Loss from operations |
|
(231,304 |
) |
|
|
(186,732 |
) |
Other income: |
|
|
|
||||
Change in fair value of equity investments |
|
1,130 |
|
|
|
(2,707 |
) |
Interest income |
|
17,527 |
|
|
|
21,931 |
|
Other (expense) income, net |
|
(893 |
) |
|
|
882 |
|
Total other income |
|
17,764 |
|
|
|
20,106 |
|
Loss before (provision for) benefit from income taxes |
|
(213,540 |
) |
|
|
(166,626 |
) |
(Provision for) benefit from income taxes |
|
(177 |
) |
|
|
3,213 |
|
Net loss |
|
(213,717 |
) |
|
|
(163,413 |
) |
Net loss attributable to noncontrolling interest |
|
— |
|
|
|
— |
|
Net loss attributable to Vir |
$ |
(213,717 |
) |
|
$ |
(163,413 |
) |
Net loss per share attributable to Vir, basic and diluted |
$ |
(1.56 |
) |
|
$ |
(1.22 |
) |
Weighted-average shares outstanding, basic and diluted |
|
136,653,753 |
|
|
|
134,289,620 |
|
View source version on businesswire.com: https://www.businesswire.com/news/home/20241031806056/en/
Media
Arran Attridge
Senior Vice President, Corporate Communications
aattridge@vir.bio
Investors
Richard Lepke
Senior Director, Investor Relations
rlepke@vir.bio
Source: Vir Biotechnology, Inc.
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