Diphtheria (D), Tetanus (T), Pertussis (Acellular, Component) (Pa), Hepatitis B (Rdna) (Hbv), Poliomyelitis (Inactivated) (Ipv) And Haemophilus Influenzae Type-B (Hib) Conjugate Vaccine(Glaxosmithkline Plc)

Collaboration leverages HilleVax’s leading norovirus vaccine development expertise and adds a Phase 1-ready next-generation program to HilleVax’s pipelineBOSTON and CHENGDU, China, Jan. 08, 2024 (GLOBE NEWSWIRE) -- HilleVax, Inc. (Nasdaq: HLVX), a clinical-stage biopharmaceutical company focused on developing and commercializing novel vaccines, and Chengdu Kanghua Biological Products Co., Ltd. (Kangh) (SHE: 300841), a biopharmaceutical company engaged in the research, development, production, and sale of bioproducts, today announced the entry into an exclusive license agreement for rights to Kangh’s hexavalent virus-like particle (VLP) vaccine candidate for norovirus, referred to by HilleVax as HIL-216, outside of Greater China. HIL-216 includes VLPs for six of the most common norovirus genotypes, including GI.1, GII.2, GII.3, GII.4, GII.6, and GII.17. The Investigational New Drug (IND) application for HIL-216 was cleared by the U.S. FDA in September 2023. As part of the exclusive license agreement, Kangh will supply HIL-216 for use in HilleVax’s near-term clinical trials, including a Phase 1 trial that HilleVax expects to initiate in 2024. “We are extremely pleased to enter this collaboration with Kangh as we seek to build out a long-term norovirus vaccine leadership position,” said Rob Hershberg, MD, PhD, Chairman and Chief Executive Officer at Hillevax. “Our bivalent norovirus VLP vaccine candidate, HIL-214, remains the most advanced norovirus vaccine candidate in clinical development, and we are on-track to report topline safety and efficacy data in mid-2024 from our ongoing Phase 2b NEST-IN1 trial. We believe that HIL-214 will be the first norovirus vaccine submitted for registration and, if approved, would address the significant unmet medical need in infants and other at-risk populations. We further believe that HIL-216 is an exciting addition to the HilleVax portfolio as a next generation, higher valency VLP-based vaccine and is an ideal fit with the expertise, capabilities and long-term aspirations of HilleVax.” “We are delighted to partner with HilleVax, a company with world-class expertise in norovirus vaccine development and a deep commitment to making an impact on the considerable morbidity, mortality, and economic burden associated with norovirus,” said Mr. Wang Zhentao, Chairman of Kangh. “This agreement represents a significant milestone for Kangh in our aim to bring our novel pipeline of vaccine products to global markets and is representative of our significant vaccine discovery, development, and manufacturing capabilities.” HilleVax will pay Kangh an upfront payment of $15 million with the potential for additional payments of up to $255.5 million upon achieving certain development and sales milestones. Kangh is also eligible to receive a single-digit tiered royalty on net sales outside of Greater China. BFC Group, Ltd. acted as advisors to HilleVax. About HilleVax HilleVax is a clinical-stage biopharmaceutical company focused on developing and commercializing novel vaccines. Its initial program, HIL-214, is a virus-like particle (VLP) based vaccine candidate in development for the prevention of moderate-to-severe acute gastroenteritis (AGE) caused by norovirus infection. Globally, norovirus is estimated to result in over approximately 700 million cases of AGE and 200,000 deaths per year, resulting in over $4 billion in direct health system costs and $60 billion in societal costs per year. The burden of norovirus falls disproportionately on young children and older adults. For more information about HilleVax, visit the company’s website at http://www.HilleVax.com. About Kangh Chengdu Kanghua Biological Products Co., Ltd. (SHE: 300841) is a biopharmaceutical company engaged in the research, development, production, and sale of bioproducts. Established in 2004, Kangh is equipped with an animal testing center and high-tech GMP production workshops for bacterial and viral vaccines. The current product portfolio includes “ACYW135 Meningococcal Polysaccharide Vaccine” (trade name: Micin®) and “Freeze-dried Human Rabies Vaccine (Human Diploid Cells)” (trade name: HDCV®). Since its establishment, Kanghua Biological has been honored with titles such as “Postdoctoral Innovation Practice Base” and “Innovative Enterprise Cultivation in Sichuan Province” by the Ministry of Personnel and the Ministry of Science and Technology, and recognized as an “Outstanding and Honest Demonstration Unit in Sichuan Province.” The company has also obtained GMP certification from the National Medical Products Administration. In recent years, Kanghua Biological has undertaken several scientific and technological projects and applied for over a hundred patents. For more information about Kangh, please visit the website at www.kangh.com. HilleVax Forward-Looking Statements HilleVax cautions you that statements contained in this press release regarding matters that are not historical facts are forward-looking statements. The forward-looking statements are based on our current beliefs and expectations and include, but are not limited to, the potential opportunity for and benefits of HIL-216 and HIL-214, the planned initiation of a Phase 1 clinical trial of HIL-216 and the timing thereof, the expected timing of a data readout from the NEST-IN1 clinical trial, the advancement of HIL-214 to registration as the first norovirus vaccine, and longer-term market leadership plans. Actual results may differ from those set forth in this press release due to the risks and uncertainties inherent in our business, including, without limitation: we currently depend entirely on the success of HIL-214, and we have not yet completed any clinical trials of HIL-214; potential delays in the commencement, enrollment, data readouts and completion of clinical trials and preclinical studies; our dependence on third parties in connection with manufacturing, research and clinical and preclinical testing; unexpected adverse side effects or inadequate immunogenicity or efficacy of HIL-214, HIL-216 or any future vaccine candidates that may limit their development, regulatory approval, and/or commercialization; unfavorable results from clinical trials; results from prior clinical trials and studies not necessarily being predictive of future results; and unstable market and economic conditions may adversely affect our business and financial condition and the broader economy and biotechnology industry; regulatory developments in the United States and foreign countries; any future impacts to our business resulting from the military conflicts or other geopolitical developments outside our control; our reliance on intellectual property rights under our license agreements with Takeda Vaccines, Inc. and Kangh; our ability to obtain, maintain and enforce intellectual property protection for our vaccine candidates; we may use our capital resources sooner than we expect; and other risks described in our prior press releases and our filings with the Securities and Exchange Commission (SEC), including under the heading “Risk Factors” in our annual report on Form 10-K and any subsequent filings with the SEC. You are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date hereof, and we undertake no obligation to update such statements to reflect events that occur or circumstances that exist after the date hereof. All forward-looking statements are qualified in their entirety by this cautionary statement, which is made under the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. Kangh Forward-Looking Statements Kangh cautions you that statements contained in this press release regarding matters that are not historical facts are forward-looking statements. The forward-looking statements are based on our current beliefs and expectations. Actual results may differ from those set forth in this press release due to the risks and uncertainties inherent in our business, including, without limitation: the vaccine product has characteristics such as a long research and development cycle, high technical difficulty, and high research and development risks. Additionally, considering the changes in external environmental factors, there is a certain level of uncertainty regarding the clinical trial progress, results, and the successful achievement of large-scale production and sales of the product. Furthermore, the milestone payments stipulated in the agreement are subject to specific conditions, and the final milestone payment amount remains uncertain. Investors are advised to make decisions cautiously, taking note of and guarding against investment risks. Kangh will closely monitor the subsequent developments of the authorized licensing matters and promptly fulfill the obligation of information disclosure. HilleVax Contact: Shane Maltbie IR@hillevax.com +1-617-213-5054 Kangh Contact: Wennian Wu khbso@kangh.com +86-28-84882755

CHICAGO--(BUSINESS WIRE)-- ISO 13485 certified Surface Solutions Laboratories (SSG), a leading provider of coating technologies for the medical device industry, today announced that it will be showcasing its GlideMed™ sustainable, compliant coating and its 12 other coating solutions in Booth #3226 at the Medical Design & Manufacturing Conference & Expo (MD&M) in Minneapolis on October 10-11, 2023. MD&M attendees are invited to meet with SSG’s team and learn more about GlideMed™, a water-based, low friction coating for medical devices. Available in No PTFE and Low PTFE formulations, it is free from PFOS, PFOA, solvent and hexavalent chromium. Developed using established, proven coating technology, it is biocompatible, environmentally friendly, and REACH and RoHS compliant. Certain chemicals have come under increased scrutiny by the US Environmental Protection Agency and EU Medical Device Regulation. “This is a significant change for medical device companies and their design engineers who are increasingly seeking functional coatings that meet or exceed regulatory requirements,” said Kevin Hess, president of SSG. “The response to GlideMed™ from major OEM device manufacturers and their tier one suppliers has been quite positive.” Sustainable GlideMed™ coatings provide excellent adhesion and permanently bonded, low friction properties that are a good alternative to traditional PTFE coatings. Available in a variety of colors, it can be applied to multiple wire configurations, lengths and types, including nitinol, stainless steel alloys, and titanium, and medical devices such as needles, guidewires, coils, cables, mandrels, hypotubes, and continuous wire. About Surface Solutions Group, LLC Surface Solutions Group is dedicated to providing proven coating technologies and solutions for the global medical device industry, and offers 13 categories of functional coatings. With 60 years of coating industry experience, SSG’s extensive automation and state-of-the-art facility provides its customers with consistently applied coatings, and meets or exceeds its customers’ demanding performance and delivery requirements. SSG serves large medical device OEMs and their contract manufacturers, component suppliers, and R&D startups primarily in the cardiovascular, neurovascular, peripheral vascular, orthopedic, surgical, spine, and dental segments. SSG is wholly owned by the Elektrisola group, a privately held company with 19 production plants and 4,700 employees worldwide. To learn more about SSG, visit surfacesolutionsgroup.com, call 773-427-2084 or follow on LinkedIn or Twitter.