
A commercial-stage biopharmaceutical company leveraging proprietary virus-like particle platforms to develop next-generation vaccines and immunotherapeutics targeting infectious disease and immuno-oncology. VBI Vaccines builds its pipeline around two distinct but often interrelated disease categories, prioritizing targets that are challenging and underserved. Its commercial anchor is PreHevbrio (previously marketed as PreHevbri in Europe), the only FDA-approved 3-antigen hepatitis B vaccine for adults in the United States. The company's dual-platform approach spans both preventive vaccines and therapeutic immunological candidates.
VBI is headquartered in Cambridge, Massachusetts, with research facilities in Ottawa, Ontario, Canada, and a research and manufacturing site in Rehovot, Israel. This tri-site footprint supports both its commercial vaccine supply chain and active research and development programs across infectious disease and oncology.
VBI Vaccines was founded in 2007 as an early-stage biotechnology startup in Cambridge, Massachusetts. A pivotal expansion came when the company acquired Epixis SA, a French biotech that brought the proprietary enveloped VLP (eVLP) platform into VBI's portfolio. SciVac Therapeutics subsequently acquired VBI in an all-stock merger, consolidating the Sci-B-Vac hepatitis B vaccine asset with VBI's platform technologies. The merged entity retained the VBI Vaccines name and went public in 2019, trading on Nasdaq.
VBI's primary focus spans infectious disease — anchored by hepatitis B — and immuno-oncology, where VLP-based immunotherapeutics are being explored as treatment-oriented approaches. Hepatitis B remains a significant global unmet need, with an estimated 296 million people chronically infected worldwide and existing vaccines offering only two-antigen coverage. VBI's 3-antigen approach was designed to address seroconversion gaps in immunocompromised and difficult-to-immunize adult populations. The oncology arm leverages the same VLP biology to stimulate targeted immune responses against tumor antigens.
VBI's core platform is the enveloped VLP (eVLP) technology, which mimics the structure of natural viral envelopes to elicit robust and durable immune responses. Unlike conventional recombinant subunit vaccines, eVLPs present antigens in their native conformation, improving immunogenicity without requiring live virus. VBI has also developed a second-generation mRNA-launched eVLP (MLE) platform, which uses mRNA to direct in vivo production of eVLPs, combining the programmability of mRNA with the potency of VLP-based immunity. This dual-platform architecture positions the company across both prophylactic vaccine and therapeutic immunotherapy applications.
PreHevbrio (hepatitis B vaccine, recombinant, adsorbed) is VBI's commercial-stage 3-antigen hepatitis B vaccine, approved by the FDA for adults and the only such product authorized in both the US and Europe. It incorporates the S, pre-S1, and pre-S2 surface antigens of HBV, compared to the single S-antigen in legacy vaccines. The Phase III PROTECT study evaluated its immunogenicity in adults aged 18 and older, and while top-line data generated a volatile market reaction, the asset reached commercial launch and VBI announced a distribution partnership with Valneva for select European markets.
VBI-2601 (BRII-179) is a therapeutic hepatitis B candidate developed in collaboration with Brii Biosciences, designed as an immunotherapy to restore functional immune control over chronic HBV infection rather than simply suppress viral replication. Brii Biosciences reported durable hepatitis B surface antigen loss in a Phase II analysis in April 2026, representing a meaningful functional cure signal. The asset leverages VBI's eVLP platform to present HBV antigens and reactivate exhausted T-cell responses.
On the coronavirus front, VBI received a commitment of up to US$33 million from CEPI to develop an eVLP vaccine candidate targeting the Beta (B.1.351) COVID-19 variant, with the partnership subsequently expanded to cover broader sarbecovirus preparedness under a renewed "Coronavirus X" collaboration.
Brii Biosciences reported positive Phase II data for VBI-2601 (BRII-179) in April 2026, showing durable control of hepatitis B surface antigen — a key functional cure marker — strengthening the therapeutic HBV program's clinical rationale. In June 2024, VBI and Valneva announced a distribution partnership for PreHevbri across select European markets, broadening the commercial reach of the 3-antigen hepatitis B franchise. Brii Biosciences also entered a second licensing agreement with VBI around the same period, signaling expanded collaboration beyond the initial VBI-2601 deal and sending VBI's pre-market shares up nearly 10%. CEPI's expanded "Coronavirus X" partnership further diversified VBI's non-HBV pipeline with pandemic-preparedness funding.
Jeffrey Baxter serves as President and Chief Executive Officer. He joined VBI in September 2009 following a role as managing partner at The Column Group, a life sciences venture capital firm, and has guided the company through its public listing and commercial launch of PreHevbrio. The management team collectively brings over 50 years of experience in immunology, vaccinology, and pharmaceutical industry development across the company's US, Canadian, and Israeli operations.
VBI's most significant collaboration is with Brii Biosciences, a China-based biotech, covering the co-development of VBI-2601 (BRII-179) as a therapeutic HBV immunotherapy; Brii entered a second agreement with VBI in June 2024, expanding the relationship. CEPI committed up to US$33 million for VBI's eVLP-based coronavirus vaccine program, with the scope subsequently broadened to address a wider range of betacoronaviruses. The Valneva distribution agreement for PreHevbri in select European markets adds a commercial-stage partnership to complement VBI's pipeline collaborations.
Existing hepatitis B vaccines contain only the S-antigen surface protein, leaving a meaningful proportion of adults — particularly immunocompromised patients, dialysis patients, and older individuals — with suboptimal immune responses. PreHevbrio incorporates three surface antigens (S, pre-S1, and pre-S2), generating broader and more durable immunity in populations that historically fail to seroconvert. VBI also extends the HBV franchise into therapeutic territory through VBI-2601, targeting the estimated 296 million people living with chronic HBV infection globally.
VBI's eVLP platform presents antigens in their native, membrane-associated conformation — mimicking the surface of an actual virus without containing genetic material capable of replication. This structural fidelity drives stronger and more relevant immune responses compared to soluble recombinant proteins. The MLE (mRNA-launched eVLP) second-generation platform extends this biology by using mRNA to direct in vivo eVLP assembly, combining the rapid programmability of mRNA technology with the immunological potency of particle-based display.
Standard HBV antivirals such as nucleos(t)ide analogs suppress viral replication but rarely achieve functional cure, requiring indefinite treatment in most patients. VBI-2601 (BRII-179) is designed to restore the immune system's ability to control HBV by reactivating exhausted CD8+ T-cell responses using eVLP-presented antigens. Brii Biosciences' Phase II data published in April 2026 showed durable hepatitis B surface antigen loss in treated patients — a surrogate marker for functional cure that current antivirals almost never achieve.
PreHevbrio is commercially available in the United States as the only FDA-approved 3-antigen hepatitis B vaccine for adults, with VBI having announced the commercial launch on Nasdaq-moving terms. In Europe, the same vaccine is marketed as PreHevbri, and VBI entered a distribution agreement with French vaccines specialist Valneva in June 2024 to expand its reach across select European markets. The Phase III PROTECT study supported the US approval, though its top-line data release triggered significant share price volatility despite the underlying regulatory success.
Beyond HBV, VBI's pipeline addresses coronavirus pandemic preparedness through a CEPI-funded eVLP vaccine program originally targeting the Beta COVID-19 variant and later broadened to cover a wider sarbecovirus threat landscape under an expanded partnership worth up to US$33 million. The company also has stated ambitions in immuno-oncology, where its VLP platform is intended to stimulate tumor-directed immune responses. The two therapeutic domains — infectious disease and oncology — are linked by the company's underlying immunological belief that appropriately powered immune responses can address both viral and malignant diseases.
VBI is commercial-stage in hepatitis B prevention, with PreHevbrio generating revenue in both the US and select European markets through the Valneva distribution deal. Its lead pipeline asset, VBI-2601, is in Phase II for therapeutic HBV, with Brii Biosciences reporting durable functional cure signals in April 2026. The CEPI-partnered coronavirus eVLP program is in earlier development, providing a longer-horizon catalyst independent of the HBV franchise.
Key catalysts and risks to monitor include:
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