– Prior data from the Phase 2 SOLSTICE trial in
chronic hepatitis delta participants demonstrated that after only
12 weeks of combination therapy, 100% (6/6) of participants had HDV
RNA less than the lower limit of quantification –
– Phase 2 SOLSTICE trial on track to complete
enrollment ahead of schedule with initial data expected in the
second quarter; greater than 90% of participants dosed –
– Prior Phase 2 MARCH Part B chronic hepatitis
B data demonstrated that tobevibart may play an important role in
achieving a functional cure; 48-week end of treatment data readout
on track for the fourth quarter –
– $1.63 billion in cash, cash equivalents and
investments as of December 31, 2023 –
– Conference call scheduled for February 22,
2024 at 1:30 p.m. PT / 4:30 p.m. ET –
Vir Biotechnology, Inc. (Nasdaq: VIR) today provided a corporate
update and reported financial results for the fourth quarter and
full year ended December 31, 2023.
“Vir is poised to have a transformational year, with catalysts
expected in the second and fourth quarters, which build off last
year’s clinical trial progress in our chronic hepatitis delta and B
programs. We believe these data readouts, notably the SOLSTICE
delta update in the second quarter, hold tremendous promise for
patients as we work towards solutions for these deadly diseases,”
said Marianne De Backer, M.Sc., Ph.D., MBA, Vir’s Chief Executive
Officer. “Our financial strength allows us to fund multiple
clinical programs through major inflection points while enabling
the flexibility to invest in external innovation
opportunities.”
Pipeline Programs
Chronic Hepatitis Delta (CHD)
- The Company presented initial SOLSTICE data from a small subset
of participants in a late-breaker presentation at the American
Association for the Study of Liver Diseases (AASLD) The Liver
Meeting in November 2023.
- After 12 weeks of combination treatment with tobevibart and
elebsiran, 5 out of 6 participants achieved undetectable HDV RNA
and 6 out of 6 were below the lower limit of quantification.
- The SOLSTICE trial is ongoing with enrollment currently ahead
of schedule for completion in the first quarter of 2024 due to the
high level of physician and patient interest. This portion of the
SOLSTICE trial is investigating the combination of tobevibart and
elebsiran given every 4 weeks in one cohort, and tobevibart
monotherapy given every 2 weeks in another cohort. Of the 30
participants anticipated to be enrolled in each cohort,
approximately 44% have compensated cirrhosis.
- The Company expects to report data on a subset of participants
in the second quarter: 12-week treatment data for 15 participants
per regimen as well as 24-week data for 10 participants per
regimen. Complete 24-week treatment data for 30 participants per
regimen is expected in the fourth quarter of 2024.
Chronic Hepatitis B (CHB)
- The Company presented new MARCH Part B data at AASLD The Liver
Meeting in November 2023.
- The data demonstrated an approximately three-fold higher
response rate when adding tobevibart to a regimen of elebsiran with
or without peginterferon after 24 weeks of treatment (15.0% for
tobevibart + elebsiran + peginterferon alpha and 14.3% for
tobevibart + elebsiran).
- The MARCH Part B trial is ongoing with 48-week end of treatment
data expected in the fourth quarter of 2024.
- The Phase 2 PREVAIL platform trial and its THRIVE/STRIVE
sub-protocols are ongoing. The platform is evaluating combinations
of tobevibart, elebsiran and/or peginterferon alpha in two CHB
patient populations with the potential to evaluate other
populations in the future. Initial data from this platform trial is
expected in the first half of 2025.
Human Immunodeficiency Virus (HIV)
- The Phase 1 trial of VIR-1388, an investigational novel T cell
vaccine for the prevention of HIV, remains ongoing with initial
immunogenicity data expected in the second half of 2024.
- The trial is supported by the National Institute of Allergy and
Infectious Diseases, part of the National Institutes of Health, and
the Bill & Melinda Gates Foundation, and is being conducted by
the HIV Vaccine Trials Network.
- In December, Nature Medicine recognized the Phase 1 trial of
VIR-1388 as one of the “11 clinical trials that will shape medicine
in 2024”.
COVID-19
- Later this year, the Company expects to file a health authority
application to support a Phase 1 trial evaluating VIR-7229, a
potential broadly neutralizing next-generation COVID antibody that
has been AI-engineered to have increased potency, breadth and
resistance to viral escape.
- The development of VIR-7229 has been supported in whole or in
part with federal funds from the Department of Health and Human
Services (HHS); Administration for Strategic Preparedness and
Response (ASPR); Biomedical Advanced Research and Development
Authority (BARDA), under Other Transaction Number:
75A50122C00081.
Influenza
- The full analysis of data from the Phase 2 PENINSULA trial is
expected in the second quarter in a scientific publication.
- On February 21, 2024, the Company and GSK terminated their
collaboration to research, develop and commercialize the Company’s
monoclonal antibodies for the prevention, treatment, or prophylaxis
of the influenza virus under the Definitive Collaboration Agreement
established in May 2021 to reflect that Vir retains sole rights to
continue advancing its investigational therapies for influenza
independently or with other partners.
- The Company is actively pursuing external partnership
opportunities for its next-generation influenza A and B antibodies
and Antibody Drug Conjugates (ADCs).
Preclinical Pipeline Candidates
- Vir is continuing to advance next-generation antibodies using
its proprietary platform, which leverages dAIsYTM (data
AI structure and antibody), an AI engine,
allowing the Company to bring high-quality drug candidates to the
clinic more efficiently.
- The Company expects the filing of multiple new INDs in the next
12-24 months, including:
- VIR-2981, an investigational neuraminidase-targeting mAb
against both influenza A and B viruses.
- VIR-8190, an investigational mAb against respiratory syncytial
virus (RSV) and human metapneumovirus.
- VIR-1949, an investigational therapeutic T cell vaccine based
on Vir’s human cytomegalovirus (HCMV) vector platform that is
designed to treat precancerous lesions caused by the human
papillomavirus.
Corporate Update
- In December of 2023, the Company announced strategic
imperatives to focus its capital allocation on programs with the
highest potential for patient impact and value creation, which
include:
- Closing R&D facilities in St. Louis, Missouri and Portland,
Oregon in 2024. Research activities will continue at the Company’s
sites in San Francisco, California and Bellinzona,
Switzerland.
- Eliminating approximately 12%, or 75 positions, including
reductions from the Company’s discontinuation of its small molecule
group which was initiated in the third quarter of 2023. The
reductions will be substantially completed by the end of the first
quarter of 2024.
- Through these actions, the Company expects to reduce its cost
structure by at least $40 million annually.
- On February 20, 2024, the Company announced that Executive Vice
President and Chief Medical Officer, Phil Pang, M.D., Ph.D., has
decided to step down to spend more time with his family. Dr. Pang’s
last day will be March 31, 2024. The Company has initiated a search
for a successor.
Fourth Quarter and Full Year 2023
Financial Results
Cash, Cash Equivalents and Investments: As of December
31, 2023, the Company had approximately $1.63 billion in cash, cash
equivalents and investments. Cash, cash equivalents and investments
declined by approximately $108 million during the fourth quarter of
2023.
Revenues: Total revenues for the quarter ended December
31, 2023 were $16.8 million compared to $49.4 million for the same
period in 2022. Total revenues for the full year of 2023 were $86.2
million compared to $1.6 billion in 2022.
Revenues were comprised of the following components:
Three Months Ended
December 31,
Year Ended December
31,
2023
2022
% Change
2023
2022
% Change
(in millions)
(in millions)
Collaboration revenue
$
8.9
$
21.6
(58.8
)%
$
37.3
$
1,505.5
(97.5
)%
Contract revenue
0.7
0.2
>100.0%
2.2
52.7
(95.8
)%
License revenue from a related party
—
—
—
%
—
22.3
(100.0
)%
Grant revenue
7.2
27.6
(73.9
)%
46.7
35.3
32.3
%
Total revenues
$
16.8
$
49.4
(66.0
)%
$
86.2
$
1,615.8
(94.7
)%
Note: Numbers may not add due to
rounding.
- Collaboration revenue: The decrease in collaboration
revenue for the fourth quarter and the full year of 2023 compared
to the same periods in 2022 was driven by lower profit share from
sales of sotrovimab under the Company’s 2020 GSK agreement.
- Contract revenue: Contract revenue for the fourth
quarter of 2023 and 2022 was nominal. The decrease in contract
revenue for the full year of 2023 compared to 2022 was primarily
driven by the recognition of deferred revenue related to GSK’s
selection of RSV in the third quarter of 2022 under the Company’s
2021 GSK agreement.
- License revenue from a related party: The decrease in
license revenue for the full year of 2023 compared to 2022 was
driven by certain revenues recognized under the collaboration with
Brii Biosciences in the third quarter of 2022.
- Grant revenue: The decrease in grant revenue for the
fourth quarter of 2023 compared to the same period in 2022 and the
increase in grant revenue for the full year of 2023 compared to
2022 were primarily driven by the timing of revenue recognized
under the Company’s grant with BARDA supporting the Company’s Phase
2 PENINSULA trial of VIR-2482.
Cost of Revenue: Cost of revenue for the fourth quarter
of 2023 was nominal compared to $6.0 million for the same period in
2022. Cost of revenue for the full year of 2023 was $2.8 million
compared to $146.3 million in 2022. The decreases were due to lower
third-party royalties owed on the sales of sotrovimab.
Research and Development Expenses (R&D): R&D
expenses for the fourth quarter of 2023 were $111.9 million, which
included severance charges of $2.6 million and $16.5 million of
non-cash stock-based compensation expense, compared to $155.2
million for the same period in 2022, which included $13.4 million
of non-cash stock-based compensation expense. The decrease was
primarily driven by the wind down of clinical studies involving
VIR-2482 in the fourth quarter of 2023. R&D expenses for the
full year of 2023 were $589.7 million, which included $62.7 million
of non-cash stock-based compensation expense, compared to $474.6
million in 2022, which included $53.2 million of non-cash
stock-based compensation expense. The increase was primarily driven
by the Phase 2 PENINSULA trial of VIR-2482 and related
manufacturing costs and, to a lesser extent, the advancement of our
CHB and CHD clinical programs.
Selling, General and Administrative Expenses (SG&A):
SG&A expenses for the fourth quarter of 2023 were $43.1
million, which included $1.9 million of severance charges and $11.8
million of non-cash stock-based compensation expense, compared to
$38.7 million for the same period in 2022, which included $11.5
million of non-cash stock-based compensation expense. SG&A
expenses for the full year of 2023 were $178.0 million, which
included $48.6 million of non-cash stock-based compensation
expense, compared to $161.8 million in 2022, which included $48.9
million of non-cash stock-based compensation expense. The increase
for both the fourth quarter and full year were primarily driven by
higher personnel-related costs.
Other Income (Loss): Other income for the fourth quarter
of 2023 was $18.3 million compared to other loss of $(1.1) million
for the same period in 2022. The increase was primarily due to
higher foreign exchange loss incurred in the fourth quarter of
2022, partially offset by higher unrealized loss of equity
investments in the same period of 2023. Other income for the full
year of 2023 was $56.1 million compared to other loss of $(78.8)
million in 2022. The increase was primarily due to higher
unrealized loss of equity investments incurred in 2022 and higher
interest income earned in 2023.
Benefit from (Provision for) Income Taxes: Benefit from
income taxes for the fourth quarter of 2023 was $4.8 million
compared to $50.0 million for the same period in 2022. Benefit from
income taxes for the year of 2023 was $13.1 million compared to a
provision for income taxes of $(238.4) million in 2022. The benefit
from income taxes in the fourth quarter and the year of 2023 was
primarily due to a pre-tax loss and our ability to carry back the
R&D credit to 2022. The benefit from income taxes in the fourth
quarter of 2022 was primarily due to the Company’s pre-tax loss.
The swing from a provision for income taxes in 2022 to a benefit
from income taxes in 2023 was due to the higher collaboration
revenue from sotrovimab sales that resulted in pre-tax income in
2022.
Net (Loss) Income: Net loss attributable to Vir for the
fourth quarter of 2023 was $(116.0) million, or $(0.86) per share,
basic and diluted, compared to a net loss of $(101.6) million, or
$(0.76) per share, basic and diluted, for the same period in 2022.
Net loss attributable to Vir for the year of 2023 was $(615.1)
million, or $(4.59) per share, basic and diluted, compared to a net
income of $515.8 million, or $3.89 per share, basic and $3.83 per
share, diluted, in 2022.
2024 Financial Guidance
Vir is providing full year 2024 guidance below (in
millions):
GAAP combined R&D and SG&A expense
range:
$
650
to
$
680
The following expenses are included in the
GAAP combined R&D and SG&A expense range:
Stock-based compensation expense
$
115
to
$
105
Restructuring charges*
$
35
to
$
25
* Restructuring charges are primarily
non-cash expenditures, related to the closing of two R&D sites
previously announced on December 13, 2023.
Approximately three to four percent of the GAAP combined R&D
and SG&A expense will be funded by grants. These grants are
recognized as revenue.
The GAAP combined R&D and SG&A 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 fourth quarter
and full year 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
Tobevibart is an investigational subcutaneously administered
antibody designed to block entry of hepatitis B and hepatitis delta
viruses into hepatocytes and to reduce the level of virions and
subviral particles in the blood. Tobevibart, which incorporates
Xencor’s Xtend™ and other Fc technologies, has been engineered to
potentially function as a T cell vaccine against hepatitis B virus
and hepatitis delta virus, as well as to have an extended
half-life. Tobevibart was identified using Vir’s proprietary mAb
discovery platform.
About Elebsiran
Elebsiran is an investigational subcutaneously administered
hepatitis B virus-targeting small interfering ribonucleic acid
(siRNA) that Vir believes has the potential to stimulate an
effective immune response and have direct antiviral activity
against hepatitis B virus and hepatitis delta virus. It is the
first siRNA in the clinic to include Enhanced Stabilization
Chemistry Plus (ESC+) technology to enhance stability and minimize
off-target activity, which potentially could result in an increased
therapeutic index. Elebsiran is the first asset in the Company’s
collaboration with Alnylam Pharmaceuticals, Inc. to enter clinical
trials.
About VIR-2482
VIR-2482 is an investigational hemagglutinin targeting,
intramuscularly administered influenza A-neutralizing monoclonal
antibody. In vitro, it has been shown to cover all major strains of
influenza A that have arisen since the 1918 flu pandemic. VIR-2482
is designed as a prophylactic for influenza A. VIR-2482
incorporates Xencor’s Xtend™ and was identified using Vir’s
proprietary mAb discovery platform.
The PENINSULA trial has been supported in whole or in part with
federal funds from the Department of Health and Human Services
(HHS); Administration for Strategic Preparedness and Response
(ASPR); Biomedical Advanced Research and Development Authority
(BARDA), under Other Transaction Number: 75A50122C00081.
About VIR-2981
VIR-2981 is an investigational neuraminidase-targeting
monoclonal antibody against influenza viruses. It targets a region
of the neuraminidase protein that is highly conserved across
influenza A and B strains and is designed to inhibit the influenza
neuraminidase, a key viral protein that facilitates release of new
viruses in infected individuals. Preclinical data demonstrate the
antibody’s breadth and potency against all major strains of
seasonal and pandemic influenza viruses and support the potential
of this antibody in the prevention of influenza illness. VIR-2981
was identified using Vir’s proprietary mAb discovery platform.
About VIR-1388
VIR-1388 is a preclinical subcutaneously administered HIV T cell
vaccine based the T cell-based viral vector platform and has been
designed to elicit abundant T cells that recognize HIV epitopes
with the goal of creating a safe and effective HIV vaccine.
About Sotrovimab
Sotrovimab is an investigational SARS-CoV-2 neutralizing
monoclonal antibody that was developed in collaboration with GSK.
The antibody binds to an epitope on SARS-CoV-2 shared with
SARS-CoV-1 (the virus that causes SARS). Sotrovimab, which
incorporates Xencor, Inc.’s Xtend™ technology, has been designed to
achieve high concentration in the lungs to achieve optimal
penetration into airway tissues affected by SARS-CoV-2 and to have
an extended half-life. Sotrovimab was identified using Vir’s
proprietary mAb discovery platform. Sotrovimab is currently not
authorized in the US.
About VIR-7229
VIR-7229 is an investigational next generation COVID-19
monoclonal antibody with a distinct combination of potency, breadth
and viral inescapability. VIR-7229 is designed as a prophylactic
for COVID-19 and was identified using Vir’s proprietary mAb
discovery platform. VIR-7229 incorporates Xencor, Inc.’s Xtend™
technology and is affinity matured using machine learning to
increase its effectiveness in binding to SARS-CoV and SARS-CoV-2
variants.
The development of VIR-7229 has been supported in whole or in
part with federal funds from the Department of Health and Human
Services (HHS); Administration for Strategic Preparedness and
Response (ASPR); Biomedical Advanced Research and Development
Authority (BARDA), under Other Transaction Number:
75A50122C00081.
About VIR-8190
VIR-8190 is an investigational dual specificity monoclonal
antibody that has the ability to potently neutralize both
respiratory syncytial virus (RSV) and human metapneumovirus (hMPV)
strains. RSV and HMPV are recognized as significant causes of lower
respiratory tract disease in high-risk populations, including
infants and immunocompromised individuals. VIR-8190 was identified
using Vir’s proprietary mAb discovery platform.
About VIR-1949
VIR-1949 is an investigational therapeutic vaccine based the T
cell-based viral vector platform that is designed to treat
HPV-related high-grade squamous epithelial pre-cancer lesions
(HSIL) and cancers. This vaccine uses HCMV as the vaccine vector.
Based on preclinical data, HCMV vectors have the potential to
induce high frequencies of antigen-specific, tissue-localizing
effector memory T cells.
About Vir Biotechnology, Inc.
Vir Biotechnology, Inc. is an immunology company focused on
powering the immune system to transform lives by treating and
preventing infectious diseases and other serious conditions,
including viral-associated diseases. Vir has assembled two
technology platforms that are designed to modulate the immune
system by exploiting critical observations of natural immune
processes. Its current clinical development pipeline consists of
product candidates targeting hepatitis delta and hepatitis B
viruses and human immunodeficiency virus. Vir has several
preclinical candidates in its pipeline, including those targeting
influenza A and B, COVID-19, RSV/MPV and HPV. 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 “may,” “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
strategy and plans; Vir’s cash balance; Vir’s financial guidance;
Vir’s future financial and operating results and its expectations
related thereto; potential of, and expectations for, Vir’s
pipeline; Vir’s clinical and preclinical development programs,
clinical trials, including the enrollment of Vir’s clinical trials,
and the expected timing of data readouts and presentations; the
potential benefits, safety, and efficacy of Vir’s investigational
therapies; and risks and uncertainties associated with drug
development and commercialization. Many important factors may cause
differences between current expectations and actual results,
including uncertainty as to whether the anticipated benefits of the
BARDA collaboration can be achieved; unexpected safety or efficacy
data or results observed during clinical trials or in data
readouts; the timing and outcome of Vir’s planned interactions with
regulatory authorities; difficulties in obtaining regulatory
approval; uncertainty as to whether the anticipated benefits of
Vir’s collaborations with other companies can be achieved;
difficulties in collaborating with other companies; challenges in
accessing manufacturing capacity; clinical site activation rates or
clinical trial enrollment rates that are lower than expected;
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 trials, Vir’s use of artificial intelligence and machine
learning in its efforts to engineer next-generation proteins and in
other research and development efforts; the timing and amount of
actual expenses, including, without limitation, Vir’s anticipated
combined GAAP R&D and SG&A expenses; geopolitical changes
or other external factors; 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 trials may not be indicative of full results
or results from later-stage or larger-scale clinical trials 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 U.S. Securities and Exchange
Commission, including the section titled “Risk Factors” contained
therein. Except as required by law, Vir assumes no obligation to
update any forward-looking statements contained herein to reflect
any change in expectations, even as new information becomes
available.
VIR BIOTECHNOLOGY,
INC.
Condensed Consolidated Balance
Sheets
(in thousands, except share
and per share data)
(unaudited)
December 31,
2023
2022
ASSETS
CURRENT ASSETS:
Cash and cash equivalents
$
241,576
$
848,631
Short-term investments
1,270,980
1,521,517
Restricted cash and cash equivalents,
current
13,268
12,681
Equity investments
9,853
31,892
Prepaid expenses and other current
assets
52,549
104,356
Total current assets
1,588,226
2,519,077
Intangible assets, net
22,565
32,755
Goodwill
16,937
16,937
Property and equipment, net
96,018
105,609
Operating right-of-use assets
71,182
82,557
Restricted cash and cash equivalents,
noncurrent
6,448
6,656
Long-term investments
105,275
23,927
Other assets
12,409
14,570
TOTAL ASSETS
$
1,919,060
$
2,802,088
LIABILITIES AND STOCKHOLDERS’
EQUITY
CURRENT LIABILITIES:
Accounts payable
$
6,334
$
6,422
Accrued and other liabilities
104,220
489,090
Deferred revenue, current
64,853
15,517
Total current liabilities
175,407
511,029
Deferred revenue, noncurrent
1,526
53,207
Operating lease liabilities,
noncurrent
111,673
123,837
Contingent consideration, noncurrent
25,960
24,937
Other long-term liabilities
14,258
11,115
TOTAL LIABILITIES
328,824
724,125
Commitments and contingencies (Note
10)
STOCKHOLDERS’ EQUITY:
Preferred stock, $0.0001 par value;
10,000,000 shares authorized as of December 31, 2023 and 2022,
respectively; no shares issued and outstanding as of December 31,
2023 and 2022
—
—
Common stock, $0.0001 par value;
300,000,000 shares authorized as of December 31, 2023 and 2022,
respectively; 134,781,286 and 133,236,687 shares issued and
outstanding as of December 31, 2023 and 2022, respectively
13
13
Additional paid-in capital
1,828,862
1,709,835
Accumulated other comprehensive loss
(815
)
(9,122
)
(Accumulated deficit) retained
earnings
(237,824
)
377,237
TOTAL STOCKHOLDERS’ EQUITY
1,590,236
2,077,963
TOTAL LIABILITIES AND STOCKHOLDERS’
EQUITY
$
1,919,060
$
2,802,088
VIR BIOTECHNOLOGY,
INC.
Condensed Consolidated
Statements of Operations
(in thousands, except share
and per share data)
(unaudited)
Three Months Ended
December 31,
Year Ended December
31,
2023
2022
2023
2022
Revenues:
Collaboration revenue
$
8,858
$
21,609
$
37,266
$
1,505,469
Contract revenue
744
180
2,228
52,714
License revenue from a related party
—
—
—
22,289
Grant revenue
7,185
27,621
46,686
35,325
Total revenues
16,787
49,410
86,180
1,615,797
Operating expenses:
Cost of revenue
798
5,996
2,765
146,319
Research and development
111,915
155,173
589,671
474,648
Selling, general and administrative
43,090
38,743
178,049
161,762
Total operating expenses
155,803
199,912
770,485
782,729
(Loss) income from operations
(139,016
)
(150,502
)
(684,305
)
833,068
Other income (loss):
Change in fair value of equity
investments
(992
)
8,879
(21,888
)
(111,140
)
Interest income
20,736
16,172
86,990
28,092
Other (expense) income, net
(1,485
)
(26,187
)
(8,991
)
4,260
Total other income (loss)
18,259
(1,136
)
56,111
(78,788
)
(Loss) income before benefit from
(provision for) income taxes
(120,757
)
(151,638
)
(628,194
)
754,280
Benefit from (provision for) income
taxes
4,784
50,035
13,077
(238,443
)
Net (loss) income
$
(115,973
)
$
(101,603
)
$
(615,117
)
$
515,837
Net loss attributable to noncontrolling
interest
$
—
$
—
$
(56
)
$
—
Net (loss) income attributable to Vir
$
(115,973
)
$
(101,603
)
$
(615,061
)
$
515,837
Net (loss) income per share attributable
to Vir, basic
$
(0.86
)
$
(0.76
)
$
(4.59
)
$
3.89
Net (loss) income per share attributable
to Vir, diluted
$
(0.86
)
$
(0.76
)
$
(4.59
)
$
3.83
Weighted-average shares outstanding,
basic
134,608,811
133,154,960
134,130,924
132,606,767
Weighted-average shares outstanding,
diluted
134,608,811
133,154,960
134,130,924
134,810,908
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version on businesswire.com: https://www.businesswire.com/news/home/20240222740501/en/
Media Carly Scaduto Senior Director, Media Relations
cscaduto@vir.bio +1 314-368-5189
Investors Richard Lepke Senior Director, Investor
Relations rlepke@vir.bio +1 978-973-9986
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