VBI Vaccines Reports First Quarter 2024 Financial Results
VBI Vaccines (NASDAQ: VBIV) reported substantial growth in its first quarter 2024 financial results. Global net revenue for PreHevbrio, their Hepatitis B vaccine, surged 105% year-over-year to $1.0 million. VBI-1901, their cancer vaccine, showed encouraging early data in glioblastoma patients, with more results expected later in 2024. The company expanded its strategic partnership with the Canadian Government to develop its MLE technology, backed by CAD$28 million in funding. Financial highlights include a decrease in cost of revenues to $2.7 million and a reduction in R&D expenses to $2.6 million. Despite net losses, the company reduced its operating cash outflow by 46% year-over-year. SG&A expenses dropped 42% due to organizational changes.
- PreHevbrio net revenue increased 105% YoY to $1.0 million.
- Early tumor response data from VBI-1901 in glioblastoma was encouraging, showing a 40% disease control rate.
- Expansion of strategic partnership with the Canadian Government, supported by CAD$28 million in funding.
- Significant reduction in cost of revenues to $2.7 million from $3.6 million YoY.
- R&D expenses decreased to $2.6 million from $3.2 million YoY.
- SG&A expenses reduced to $7.7 million from $13.3 million YoY.
- 46% decrease in net cash used in operating activities, from $21.7 million to $11.8 million YoY.
- Net loss per share decreased from $3.22 to $0.73 YoY.
- Cash position dropped to $12.6 million from $23.7 million at the end of 2023.
- Net loss for Q1 2024 was $17.9 million, down from $27.8 million in Q1 2023.
- High foreign exchange loss of $4.3 million.
- Net revenues were still relatively low at $1.2 million despite growth.
- Continued reliance on organizational changes to reduce costs.
- Ongoing dependency on funding and strategic partnerships to support R&D.
VBI Vaccines reported a significant 105% year-over-year increase in net revenue for PreHevbrio in the first quarter of 2024. Such substantial growth in product revenue highlights strong market adoption and effective commercial execution. Despite this revenue growth, the company continues to face challenges in terms of profitability. The net loss for Q1 2024 was
The preliminary results from the Phase 2b study of VBI-1901 in recurrent glioblastoma (GBM) patients are worth noting. The 40% disease control rate achieved in the VBI-1901 arm contrasts sharply with the control arm's 0% rate, where all evaluable patients had significant tumor progression. This suggests that VBI-1901 might offer a potential therapeutic benefit over existing chemotherapies, which is significant for a condition with limited effective treatments. Investors should keep an eye on the additional tumor response data expected mid-year and initial survival data by year-end, as these results will be important in validating the efficacy of VBI-1901 and could lead to substantial valuation changes for VBI Vaccines if positive.
The evaluation of VBI’s novel mRNA-launched eVLP (MLE) platform technology by potential partners is another key development. This platform could be transformative for VBI, given the increasing interest in mRNA technology following the success of mRNA COVID-19 vaccines. The partnership with the Canadian Government, supported by a substantial
-
PreHevbrio® (Hepatitis B Vaccine [Recombinant]) global net revenue increased
105% year-over-year in the first quarter of 2024 compared to the first quarter of 2023 - Initial encouraging tumor response data from randomized Phase 2b study of VBI-1901 in recurrent glioblastoma (GBM) announced in April – additional data expected mid-year and year-end 2024
- Evaluation of novel mRNA-launched eVLP (MLE) platform technology underway by potential partners
“To date in 2024, our focus has centered around pipeline execution, expanding access and increased uptake of PreHevbrio in targeted market segments, and execution of strategic partnerships to drive opportunity for our portfolio assets, create shareholder value, and strengthen our balance sheet,” said Jeff Baxter, VBI’s President and CEO. “We remain committed to creating opportunities for our vaccines, candidates, and technologies to meaningfully impact public health and the lives of patients, providers, and families.”
Recent Key Program Achievements and Projected Upcoming Milestones
PreHevbrio® [Hepatitis B Vaccine (Recombinant)]
-
Product revenue, net increased
105% from Q1 2023, with earned in Q1 2024$1.0 million -
US:
-
H1 2024 PreHevbrio
U.S. sales continue to demonstrate substantial growth over 2023, with over80% of the 2023 full-year volume being sold in the first five months of 2024 - Commercial execution in Q1 2024 created new demand in the large Integrated Delivery Network (IDN) and hospital system space, and saw continued national and regional pharmacy uptake
- Public sector momentum building with PreHevbrio now available for purchase under the CDC Adult Vaccine Contract
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H1 2024 PreHevbrio
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Ex-US – PreHevbri®:
- VBI partners with Valneva SE to make PreHevbri available in certain European countries
-
In 2023, through this partnership, PreHevbri was launched in the
UK ,Sweden ,Netherlands , andBelgium – in early 2024, PreHevbri also became available inDenmark andNorway
VBI-1901: Cancer Vaccine Immunotherapeutic Candidate – Glioblastoma (GBM)
- VBI-1901 is being evaluated in an ongoing, randomized, controlled Phase 2b study in comparison to standard-of-care chemotherapy treatment in recurrent GBM patients
-
April 2024: Encouraging early tumor response data from Phase 2b study in recurrent GBM presented at World Vaccine Congress 2024:
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VBI-1901 Arm: 2 stable disease (SD) observations among patients eligible for evaluation at week 12 (n=2/5), achieving a
40% disease control rate, consistent with44% disease control rate observed in the Phase 1/2a portion of the study -
Control Arm (carmustine or lomustine chemotherapy): No tumor responses have been observed to date (n=0/6;
0% disease control rate) – all evaluable patients experienced a 2-8x increase in tumor size by week 6 and have been taken off study protocol
-
VBI-1901 Arm: 2 stable disease (SD) observations among patients eligible for evaluation at week 12 (n=2/5), achieving a
- Mid-Year 2024 and Year-End: Additional tumor response data from ongoing Phase 2b study expected mid-year 2024, with initial survival data from early-enrolled participants expected by year-end 2024, subject to speed of enrollment
Novel mRNA-Launched eVLP (MLE) Technology Platform
-
April 2024: Announced expansion of strategic partnership with the Canadian Government to advance the development of the MLE technology platform, supported by the
CAD funding award remaining under the original agreement$28 million - Throughout 2024: MLE technology remains under active evaluation by potential partners
Other Achievements and Upcoming Milestones
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February 2024: Announced a series of agreements with Brii Biosciences (“Brii Bio”), pursuant to which, subject to achievement of certain activities, VBI would receive up to
in consideration for VBI’s manufacturing capabilities and certain related assets at Rehovot manufacturing facility, the intellectual property for VBI-2601, VBI’s hepatitis B immunotherapeutic candidate, and a license for VBI-1901 in the$33 million Asia Pacific region, excludingJapan -
Following completion of the full transaction, target mid-year 2024, VBI expects its total debt principal to be significantly reduced to
$17 million
-
Following completion of the full transaction, target mid-year 2024, VBI expects its total debt principal to be significantly reduced to
- 2024: Additional data expected from Phase 1 study of VBI-2901, VBI’s multivalent pan-coronavirus vaccine candidate – initial data from which were reported in September 2023
Recent Peer-Reviewed Publications
-
Langley , Gantt, et al., “An enveloped virus-like particle alum-adjuvanted cytomegalovirus vaccine is safe and immunogenic: A first-in-humans Canadian Immunization Research Network (CIRN) study” published in Vaccine – Link Here
Financial Results for the Three Months Ended March 2024
-
Cash Position: As of March 31, 2024 VBI had
in cash as compared with$12.6 million in cash as of December 31, 2023. Cash position at March 31, 2024, does not include approximately$23.7 million gross proceeds from registered direct offering of common shares and warrants, warrant exercises, and sale of common shares through VBI’s at-the-market facility with Jefferies LLC, subsequent to March 31, 2024 and through early April 2024.$2.8 million -
Revenues, net: Revenues, net for the first quarter 2024 were
as compared to$1.2 million for the same period in 2023. The revenue increase was a result of an increase in product sales of PreHevbrio in the$0.5 million U.S. -
Cost of Revenues: Cost of revenues was
in the first quarter of 2024 as compared to$2.7 million in the first quarter of 2023. The decrease in the cost of revenues was a result of the April 2023 organizational changes and decreased inventory-related costs, offset by increased product sales.$3.6 million -
Research and Development (R&D): R&D expenses for the first quarter of 2024 were
as compared to$2.6 million for the same period in 2023. R&D expenses were offset by$3.2 million for the three months ended March 31, 2024, and$0.7 million for the three months ended March 31, 2023 due to government grants and funding arrangements. The decrease in R&D expenses is primarily a result of decreased development expenses for VBI’s pan-coronavirus and GBM candidates, VBI-2901 and VBI-1901, due to timing of ongoing clinical studies of each candidate.$2.4 million -
Sales, General, and Administrative (SG&A): SG&A expenses for the first quarter of 2024 were
as compared to$7.7 million in the first quarter of 2023. The decrease in SG&A expenses was mainly a result of the April 2023 organizational changes that reduced our internal workforce, commercial field teams, and operating expenses.$13.3 million -
Net Cash Used in Operating Activities: Net cash used in operating activities for the first quarter of 2024 was
compared to$11.8 million for the same period in 2023. The$21.7 million 46% decrease in cash outflows is largely due to a decrease in net loss as a result of the April 2023 organizational changes, in addition to the change in operating working capital, most notably in inventory, other current assets, accounts payable, and other current liabilities. -
Net Loss and Net Loss Per Share: Net loss and net loss per share for the first quarter of 2024 were
and$17.9 million , respectively, as compared to a net loss and net loss per share of$0.73 and$27.8 million for the first quarter of 2023, respectively.$3.22 -
Net Loss and Net Loss Per Share, Excluding Foreign Exchange Loss: Net loss and net loss per share, excluding foreign exchange loss, for the first quarter 2024 were
and$13.6 million , respectively, compared to$0.55 and$20.9 million for the first quarter 2023, respectively. See “Use of Non-GAAP Financial Measures” below for additional information regarding this non-GAAP financial measure, and “GAAP to Non-GAAP Reconciliation” for a reconciliation of this non-GAAP financial measure to net loss and net loss per share.$2.43 -
Foreign exchange loss for the first quarter of 2024 was
as compared to$4.3 million for the first quarter of 2023. Certain intercompany loans between the Company and its subsidiaries are denominated in a currency other than the functional currency of each entity. The decrease in foreign exchange loss was a result of the changes in the foreign currency exchange rates (of the New Israeli Shekel and the Canadian Dollar) in which the foreign currency transactions were denominated for each of those periods, including the foreign exchange impact of intercompany loans that are translated at period end.$6.8 million
-
Foreign exchange loss for the first quarter of 2024 was
Use of Non-GAAP Financial Measures
Net Loss, Excluding Foreign Exchange Loss, and Net Loss Per Share, Excluding Foreign Exchange Loss, are non-GAAP financial measures and are defined as Net Loss and Net Loss Per Share excluding the foreign exchange loss in both calculations. Net Loss, Excluding Foreign Exchange Loss, and Net Loss Per Share, Excluding Foreign Exchange Loss, are not intended to replace Net Loss or Net Loss Per Share or other measures of financial performance reported in accordance with generally accepted accounting principles (GAAP). VBI’s management believes that the presentation of Net Loss, Excluding Foreign Exchange Loss, and Net Loss Per Share, Excluding Foreign Exchange Loss, are useful to investors because management does not consider foreign exchange loss, which is primarily driven by changes in exchange rates related to certain intercompany loans, and is a non-recurring item, when evaluating VBI’s operating performance. Non-GAAP financial measures are meant to supplement, and to be viewed in conjunction with, GAAP financial results. The presentation of these non-GAAP financial measures should not be considered in isolation or as a substitute for comparable GAAP financial measures and should be read only in conjunction with the Company’s financial statements prepared in accordance with GAAP. Reconciliations of the Company’s non-GAAP measures are included below.
The following represents a reconciliation of Net Loss to Net Loss, Excluding Foreign Exchange Loss, and Net Loss Per Share to Net Loss Per Share, Excluding Foreign Exchange Loss. See “Non-GAAP Financial Information” below for additional information regarding this non-GAAP financial measure, and “GAAP to Non-GAAP Reconciliation” for a reconciliation of this non-GAAP financial measure to net loss and net loss per share.
GAAP to Non-GAAP Reconciliations
The following represents a reconciliation of Net Loss to Net Loss Excluding Impairment Charges and Foreign Exchange Loss and Net Loss per Share Excluding Foreign Exchange Loss.
|
Three Months Ended March 31 |
|||||||
|
2024 |
|
2023 |
|||||
|
(Unaudited) (In 000’s except share and per share amounts) |
|||||||
Net Loss |
$ |
(17,900 |
) |
$ |
(27,751 |
) |
||
Foreign exchange loss |
|
4,330 |
|
|
6,813 |
|
||
Net loss, excluding impairment charges and foreign exchange loss |
$ |
(13,570 |
) |
$ |
(20,938 |
) |
||
Weighted-average number of shares |
|
24,584,798 |
|
|
8,608,539 |
|
||
Net loss per share, excluding impairment charges and foreign exchange loss |
$ |
(0.55 |
) |
$ |
(2.43 |
) |
||
|
|
|
About PreHevbrio [Hepatitis B Vaccine (Recombinant)]
PreHevbrio is the only 3-antigen hepatitis B vaccine, comprised of the three surface antigens of the hepatitis B virus – Pre-S1, Pre-S2, and S. It is approved for use in the
Please visit www.PreHevbrio.com for
PreHevbrio is indicated for prevention of infection caused by all known subtypes of hepatitis B virus. PreHevbrio is approved for use in adults 18 years of age and older.
Do not administer PreHevbrio to individuals with a history of severe allergic reaction (e.g. anaphylaxis) after a previous dose of any hepatitis B vaccine or to any component of PreHevbrio.
Appropriate medical treatment and supervision must be available to manage possible anaphylactic reactions following administration of PreHevbrio.
Immunocompromised persons, including those on immunosuppressant therapy, may have a diminished immune response to PreHevbrio.
PreHevbrio may not prevent hepatitis B infection, which has a long incubation period, in individuals who have an unrecognized hepatitis B infection at the time of vaccine administration.
The most common side effects (>
There is a pregnancy exposure registry that monitors pregnancy outcomes in women who received PreHevbrio during pregnancy. Women who receive PreHevbrio during pregnancy are encouraged to contact 1-888-421-8808 (toll-free).
To report SUSPECTED ADVERSE REACTIONS, contact VBI Vaccines at 1-888-421-8808 (toll-free) or VAERS at 1-800-822-7967 or www.vaers.hhs.gov.
Please see Full Prescribing Information.
About VBI Vaccines Inc.
VBI Vaccines Inc. (“VBI”) is a biopharmaceutical company driven by immunology in the pursuit of powerful prevention and treatment of disease. Through its innovative approach to virus-like particles (“VLPs”), including a proprietary enveloped VLP (“eVLP”) platform technology and a proprietary mRNA-launched eVLP (“MLE”) platform technology, VBI develops vaccine candidates that mimic the natural presentation of viruses, designed to elicit the innate power of the human immune system. VBI is committed to targeting and overcoming significant infectious diseases, including hepatitis B, coronaviruses, and cytomegalovirus (CMV), as well as aggressive cancers including glioblastoma (GBM). VBI is headquartered in
Website Home: http://www.vbivaccines.com/
News and Resources: http://www.vbivaccines.com/news-and-resources/
Investors: http://www.vbivaccines.com/investors/
Cautionary Statement on Forward-looking Information
Certain statements in this press release that are forward-looking and not statements of historical fact are forward-looking statements within the meaning of the safe harbor provisions of the Private Securities Litigation Reform Act of 1995 and are forward-looking information within the meaning of Canadian securities laws (collectively, “forward-looking statements”). The Company cautions that such forward-looking statements involve risks and uncertainties that may materially affect the Company’s results of operations. Such forward-looking statements are based on the beliefs of management as well as assumptions made by and information currently available to management. Actual results could differ materially from those contemplated by the forward-looking statements as a result of certain factors, including but not limited to, the Company’s ability to regain and maintain compliance with the listing standards of the Nasdaq Capital Market, the Company’s ability to satisfy all of the conditions to the consummation of the transactions with Brii Biosciences, the Company’s ability to comply with its obligations under its loan agreement with K2 HealthVentures, the impact of general economic, industry or political conditions in
VBI Vaccines Inc. and Subsidiaries |
|||||||
Selected Condensed Consolidated Balance Sheet |
|||||||
(Unaudited, In Thousands) |
|||||||
|
Three Months Ended March 31 |
||||||
|
2024 |
|
2023 |
||||
|
(Unaudited) (In 000’s except share and per share amounts) |
||||||
Assets |
|
|
|||||
Cash |
$ |
12,595 |
|
$ |
23,685 |
||
Accounts receivable, net |
|
227 |
|
|
- |
||
Inventory, net |
|
9,944 |
|
|
8,499 |
||
Prepaid expenses and other current assets |
|
3,595 |
|
|
4,047 |
||
Total current assets |
|
26,361 |
|
|
36,231 |
||
Property and equipment, net |
|
9,088 |
|
|
9,665 |
||
Intangible assets, net |
|
35,734 |
|
|
36,499 |
||
Goodwill |
|
1,107 |
|
|
1,130 |
||
Other non-current assets |
|
3,153 |
|
|
3,426 |
||
Total Assets |
$ |
75,443 |
|
$ |
86,951 |
||
|
|
|
|||||
Liabilities and stockholders’ equity |
|
|
|||||
Accounts payable |
$ |
8,871 |
|
$ |
6,431 |
||
Other current liabilities |
|
68,723 |
|
|
69,305 |
||
Total current liabilities |
|
77,594 |
|
|
75,736 |
||
Total non-current liabilities |
|
3,316 |
|
|
3,688 |
||
Total liabilities |
|
80,910 |
|
|
79,424 |
||
Total stockholders' equity |
|
(5,467 |
) |
|
7,527 |
||
Total liabilities and stockholders' equity |
$ |
75,443 |
|
$ |
86,951 |
VBI Vaccines Inc. and Subsidiaries |
||||||||
Condensed Consolidated Statement of Operations and Comprehensive Loss |
||||||||
(Unaudited, In Thousands Except Share and Per Share Amounts) |
||||||||
|
Three Months Ended March 31 |
|||||||
|
2024 |
|
2023 |
|||||
|
(Unaudited) |
|||||||
Revenues, net |
$ |
1,214 |
|
$ |
485 |
|
||
Operating expenses |
||||||||
Cost of revenues |
|
2,724 |
|
|
3,559 |
|
||
Research and development |
|
2,571 |
|
|
3,151 |
|
||
Sales, general, and administrative |
|
7,671 |
|
|
13,284 |
|
||
Total operating expenses |
|
12,966 |
|
|
19,994 |
|
||
Loss from operations |
|
(11,752 |
) |
|
(19,509 |
) |
||
Interest expense, net of interest income |
|
(1,818 |
) |
|
(1,429 |
) |
||
Foreign exchange loss |
|
(4,330 |
) |
|
(6,813 |
) |
||
Loss before income taxes |
|
(17,900 |
) |
|
(27,751 |
) |
||
Income tax benefit |
|
- |
|
|
- |
|
||
Net Loss |
$ |
(17,900 |
) |
$ |
(27,751 |
) |
||
Basic and diluted net loss per share |
$ |
(0.73 |
) |
$ |
(3.22 |
) |
||
Weighted-average number of shares used to compute basic and diluted net loss per share |
|
24,584,798 |
|
|
8,608,539 |
|
||
Other comprehensive income |
|
3,484 |
|
|
6,599 |
|
||
Comprehensive Loss |
$ |
(14,416 |
) |
$ |
(21,152 |
) |
View source version on businesswire.com: https://www.businesswire.com/news/home/20240515040100/en/
VBI
Nicole Anderson
Director, Corporate Communications & IR
(617) 830-3031 x124
IR@vbivaccines.com
Source: VBI Vaccines Inc.
FAQ
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