mRNA Vaccine Core Enzyme Market to Reach USD 7 Billion by 2034
Luton, Bedfordshire, United Kingdom, June 16, 2025 (GLOBE NEWSWIRE) -- The global mRNA vaccine core enzyme market is witnessing unprecedented growth, driven by heightened demand for rapid vaccine development and growing advancements in biotechnology. As of 2024, the market is valued at approximately USD 2.3 billion, with projections indicating it will reach nearly USD 7 billion by 2034, reflecting a CAGR of 13.4% over the forecast period. This growth trajectory is underpinned by expanding applications of mRNA technology across infectious diseases, cancer therapeutics, and personalized medicine, along with increased public and private sector investments.
Download PDF Brochure: https://exactitudeconsultancy.com/request-sample/64421
The COVID-19 pandemic played a transformative role in bringing mRNA vaccine technologies into the spotlight, proving their potential for rapid response and scalable deployment. As governments, pharmaceutical companies, and research institutions pivot towards future pandemic preparedness and broader therapeutic applications, the core enzymes essential for mRNA synthesis and delivery—such as polymerases and lipid nanoparticles—are in increasingly high demand.
Market Segmentation Analysis
By Product Type
The market is segmented into Poly(A) Polymerase, RNA Polymerase, Nudge Enzyme, and Other Enzymes. Among these, Poly(A) Polymerase holds a dominant share due to its essential role in stabilizing synthetic mRNA transcripts for vaccine formulation. Enhanced purification techniques have also improved the quality and reliability of Poly(A) Polymerase, increasing its demand.
RNA Polymerase, equally critical, is widely used in transcription processes to synthesize mRNA from DNA templates. It finds applications in both commercial vaccine production and academic research. Nudge Enzymes, although newer to the market, are gaining traction due to their emerging role in improving mRNA stability and delivery efficiency. These innovations signal strong growth prospects, particularly for advanced research and personalized therapies.
By Application
The therapeutics segment is emerging as a key growth driver within the application spectrum, spurred by research into using mRNA technology for cancer treatment, autoimmune conditions, and rare diseases. Collaborations between biotech startups and large pharmaceutical firms are fostering the development of new therapeutic platforms leveraging mRNA enzymes.
In contrast, preventive vaccines remain the cornerstone of the mRNA enzyme market, bolstered by ongoing global vaccination programs and the anticipation of future pandemics. The success of COVID-19 mRNA vaccines has underscored the need for faster, adaptable vaccine platforms.
Research and development (R&D) also constitutes a significant market share. A surge in clinical trials and funding for pre-clinical mRNA studies—especially in academic and research institutions—continues to drive enzyme demand, particularly as R&D efforts expand to newer disease areas.
By End User
Pharmaceutical companies form the largest end-user segment, leveraging their production capacity, regulatory expertise, and global distribution networks to manufacture large volumes of mRNA-based products. These firms rely heavily on high-quality enzymes for consistent vaccine efficacy.
Academic and research institutions, while smaller in scale, play a vital role in early-stage innovation and pilot studies. They frequently collaborate with biotech firms to explore novel mRNA applications, thereby fueling demand for research-grade enzymes.
Biotech companies, particularly startups focused on gene editing and personalized medicine, represent a fast-growing end-user base. These companies require scalable and customizable enzyme solutions, thereby creating a niche yet dynamic demand profile.
By Technology
The market is further categorized by technology into In Vitro Transcription, Purification Technologies, and Quality Control and Characterization Technologies. Among these, In Vitro Transcription (IVT) is foundational to mRNA synthesis. Continued optimization has enhanced both yield and cost-efficiency, making IVT indispensable for vaccine production.
Purification technologies ensure removal of contaminants and increase product stability. Emerging trends involve automating these processes to minimize human error and improve throughput.
Meanwhile, quality control and characterization technologies are becoming increasingly vital due to stringent regulatory requirements. These technologies facilitate consistency, batch reproducibility, and compliance, making them a key area for future investments.
By Distribution Channel
Distribution of mRNA enzymes occurs through direct sales, online platforms, and third-party distributors. Direct sales remain preferred by pharmaceutical companies for custom orders and quality assurance, ensuring close coordination with enzyme manufacturers.
However, online sales are on the rise, particularly among academic institutions and smaller biotech firms looking for convenience and cost savings. The trend reflects a broader shift toward digital procurement models in the life sciences sector.
Third-party distributors serve an important role in extending enzyme availability to emerging markets and underserved regions. Their reach and logistical support are critical to ensuring timely supply in areas lacking direct access to manufacturers.
Browse full Report - https://exactitudeconsultancy.com/reports/64421/global-mrna-vaccine-core-enzyme-market
Market Segmentation
By Product Type - Poly(A) Polymerase - RNA Polymerase - Nudge Enzyme
By Application - Therapeutics - Preventive Vaccines - Research and Development
By End-user - Pharmaceutical Companies - Academic and Research Institutions - Biotech Companies
By Distribution Channel - Direct Sales - Online Sales - Third-party Distributors
By Technology - In Vitro Transcription - Purification technologies - Quality control and characterization technologies
By Region - North America - Europe - Asia Pacific - Latin America - Middle East and Africa
Regional Insights
North America
North America leads the global mRNA vaccine core enzyme market, contributing approximately 45% of global revenue in 2024. The U.S. stands at the forefront due to its robust biotech ecosystem, deep investment in R&D, and support from regulatory bodies like the FDA. Strategic collaborations between pharma giants and research institutions further accelerate innovation and commercialization. The region is expected to grow at a CAGR of around 8.5% through 2034.
Europe
Europe holds a significant market share of around 30%, led by countries like Germany, the UK, and France. Favorable government policies, strong academic research infrastructure, and a growing emphasis on biotechnology are propelling market growth. A CAGR of 7.0% is anticipated through 2034 as EU nations enhance their domestic vaccine capabilities and biotech investments.
Asia Pacific
Asia Pacific is the fastest-growing region, projected to expand at a CAGR of 10.5% by 2034. Major drivers include rising investments in health infrastructure, expanding pharmaceutical manufacturing hubs in China and India, and increasing public health awareness. However, challenges such as regulatory complexity and uneven infrastructure persist across the region.
Latin America and Middle East & Africa
Emerging markets like Latin America and Africa are exhibiting strong growth potential, driven by improvements in public health funding and localized vaccine production. Though still nascent, these regions are expected to attract future investment. Infrastructure and regulatory challenges, however, may temper the pace of growth unless addressed through public-private collaboration.
Buy Now: https://exactitudeconsultancy.com/purchase/?currency=USD&type=single_user_license&report_id=64421
Key Competitors
Moderna Inc.
BioNTech SE
Pfizer Inc.
CureVac AG
Gennova Biopharmaceuticals
Zydus Cadila
Sanofi
AstraZeneca
Merck & Co., Inc.
Novavax Inc.
Regeneron Pharmaceuticals
Translate Bio
Genexine Inc.
AbCellera Biologics
Takeda Pharmaceutical Company Limited
Recent Market Developments
Moderna Inc. expanded its mRNA production facility in Norwood, Massachusetts in August 2023, aiming to scale up production in response to growing global demand.
BioNTech SE launched a next-generation mRNA-based influenza vaccine in September 2023, signaling a shift toward seasonal applications beyond COVID-19.
CureVac AG announced a strategic partnership in July 2023 with a major pharmaceutical firm to co-develop mRNA therapies, highlighting a trend toward collaboration and shared risk.
Zydus Cadila received regulatory approval in India for its mRNA COVID-19 vaccine in October 2023, positioning the country as a significant player in localized mRNA production.
Pfizer Inc. acquired a biotech firm specializing in advanced mRNA platforms in November 2023, bolstering its pipeline and reaffirming its commitment to innovation.
This report is also available in the following languages : Japanese (mRNAワクチンコア酵素市場), Korean (mRNA 백신 핵심 효소 시장), Chinese (mRNA疫苗核心酶市场), French (Marché des enzymes de base des vaccins à ARNm), German (Markt für mRNA-Impfstoff-Kernenzyme), and Italian (Mercato degli enzimi fondamentali del vaccino mRNA), etc.
Request Sample Pages: https://exactitudeconsultancy.com/reports/64421/global-mrna-vaccine-core-enzyme-market#request-a-sample
More Research Finding –
Tozinameran Market
The global market for Tozinameran, a key COVID-19 mRNA vaccine, is valued at approximately $21 billion. The market is expected to grow significantly, with a projected value of around $45 billion by 2034. This represents a Compound Annual Growth Rate (CAGR) of about 8.1% from 2025 to 2034.
https://exactitudeconsultancy.com/reports/66480/tozinameran-market
mRNA Vaccine and Therapeutics Raw Material Market
The global market for mRNA vaccine and therapeutics raw materials is valued at approximately $4.5 billion, driven by the accelerating demand for innovative vaccine solutions and therapeutic modalities. The market is projected to reach around $9.2 billion by 2034, reflecting a robust Compound Annual Growth Rate (CAGR) of approximately 8.2% from 2025 to 2034.
https://exactitudeconsultancy.com/reports/65932/mrna-vaccine-and-therapeutics-raw-material-market
Non-invasive Vaccine Market
The global non-invasive vaccine market is projected to reach a value of approximately $2.5 billion in 2024, driven by advancements in vaccine delivery systems and increasing demand for pain-free immunization methods. During the forecast period from 2025 to 2034, the market is expected to experience significant growth, with an estimated compound annual growth rate (CAGR) of 11.5%.
https://exactitudeconsultancy.com/reports/59766/global-non-invasive-vaccine-market
Foot and Mouth Disease FMD Vaccines for Pig Market
The global market for Foot and Mouth Disease (FMD) vaccines for pigs is projected to reach approximately $1.2 billion in 2024, with a significant growth trajectory anticipated through the next decade. By 2034, the market value is expected to rise to about $2.3 billion, reflecting a robust Compound Annual Growth Rate (CAGR) of 6.9% from 2025 to 2034.
https://exactitudeconsultancy.com/reports/59747/global-foot-and-mouth-disease-fmd-vaccines-for-pig-market
Flu RNA Vaccines Market
The global market for flu RNA vaccines is valued at approximately $2.5 billion, reflecting a growing demand for innovative vaccination solutions amid rising flu cases and the ongoing need for enhanced public health measures. Projections indicate that the market will expand to around $6 billion by 2034, with a Compound Annual Growth Rate (CAGR) of 9.1% over the forecast period from 2025 to 2034.
https://exactitudeconsultancy.com/reports/55918/global-flu-rna-vaccines-market
Pediatric Vaccines Market
The global pediatric vaccines market is valued at approximately $40 billion, driven by increasing immunization rates and the growing incidence of infectious diseases among children. With advancements in vaccine technologies and rising awareness of preventive healthcare, the market is projected to reach around $70 billion by 2034, marking substantial growth.
https://exactitudeconsultancy.com/reports/52011/pediatric-vaccines-market
Shingles Vaccine Market
The global shingles vaccine market is valued at approximately $5.1 billion, driven by increasing awareness of shingles and rising vaccination rates among older populations. The market is projected to grow significantly, reaching an estimated value of $10 billion by 2034, with a Compound Annual Growth Rate (CAGR) of 7.1% from 2025 to 2034.
https://exactitudeconsultancy.com/reports/51861/shingles-vaccine-market
U.S. Meningococcal Vaccines Market
The U.S. meningococcal vaccines market is valued at approximately $1.5 billion, reflecting a robust demand driven by increasing awareness of meningococcal disease and vaccination initiatives. The market is projected to grow at a CAGR of 6.2%, reaching an estimated $2.7 billion by 2034. This growth trajectory is propelled by several factors, including expanded recommendations for vaccination among adolescents and young adults, and the ongoing efforts to enhance vaccine accessibility and education.
https://exactitudeconsultancy.com/reports/50804/u-s-meningococcal-vaccines-market
Rna Based Therapeutics Market
The RNA-based therapeutics market is projected to reach a value of approximately $7.3 billion in 2024, driven by advancements in mRNA technology and increasing investments in gene therapies. The market is expected to expand significantly with a projected value of around $19.6 billion by 2034, reflecting a robust Compound Annual Growth Rate (CAGR) of 10.4% during the forecast period from 2025 to 2034.
https://exactitudeconsultancy.com/reports/50749/rna-based-therapeutics-market
U.S. Vaccine Technologies Market
The U.S. vaccine technology market is valued at approximately $70 billion, buoyed by increasing demand for innovative vaccines and heightened awareness of public health needs. The market is projected to grow significantly, with an estimated value reaching $110 billion by 2034, reflecting a robust growth trajectory.
https://exactitudeconsultancy.com/reports/50446/u-s-vaccine-technologies-market
Chikungunya Vaccine Future Trends and Market
The global chikungunya vaccine market is projected to hold a value of approximately $2.5 billion in 2024. Given the increasing incidence of chikungunya virus infections and the growing awareness regarding preventative healthcare measures, the market is expected to reach around $5.6 billion by 2034. This outlook suggests a robust Compound Annual Growth Rate (CAGR) of 8.5% during the forecast period from 2025 to 2034.
https://exactitudeconsultancy.com/reports/50225/chikungunya-vaccine-market
Innovations in Vaccine Technologies Market
The global vaccine technologies market is projected to reach a value of approximately $65 billion in 2024, with expectations to grow to about $110 billion by 2034. This trajectory represents a compound annual growth rate (CAGR) of around 5.3% during the forecast period from 2025 to 2034.
https://exactitudeconsultancy.com/reports/50217/vaccine-technologies-market
Dendritic Cell Therapy Vaccine Market
The dendritic cell therapy vaccine market is valued at approximately $1.2 billion, reflecting a robust interest in innovative immunotherapy solutions. The market is projected to reach around $3.4 billion by 2034, indicating a substantial growth trajectory driven by advancements in personalized medicine and an increasing prevalence of cancer worldwide.
https://exactitudeconsultancy.com/reports/66582/dendritic-cell-therapy-vaccine-market
Gammaretroviral Vector Market
The gammaretroviral vector market is anticipated to reach approximately $1.2 billion in 2024, driven by advancements in gene therapies and increasing applications in biomedical research. The market is projected to grow significantly, with an estimated compound annual growth rate (CAGR) of 8.5% from 2025 to 2034, ultimately reaching around $2.7 billion by the end of this forecast period.
https://exactitudeconsultancy.com/reports/66577/gammaretroviral-vector-market
Multi Use Bioreactor Market
The global multi-use bioreactor market is valued at approximately $3.2 billion, reflecting significant growth driven by advances in biopharmaceutical manufacturing and increased demand for personalized medicine. The projected market value for 2025-2034 is estimated to reach $6.5 billion, highlighting the sector's robust expansion.
https://exactitudeconsultancy.com/reports/66574/multi-use-bioreactor-market
Medical Refrigerated Market
The global medical refrigerated market is valued at approximately $6.5 billion in 2024, with projections indicating a potential increase to around $10 billion by 2034. This growth reflects a robust Compound Annual Growth Rate (CAGR) of approximately 4.5% during the forecast period from 2025 to 2034.
https://exactitudeconsultancy.com/reports/66520/medical-refrigerated-market
Needle for Disposable Injection Pen Market
The disposable injection pen market is valued at approximately $4.5 billion in 2024, with expectations to grow significantly over the next decade, reaching an estimated $9 billion by 2034. This growth reflects a Compound Annual Growth Rate (CAGR) of around 7.5% during the forecast period from 2025 to 2034.
https://exactitudeconsultancy.com/reports/66462/needle-for-disposable-injection-pen-market
Meningitis B Vaccine Market
The global market for Meningitis B vaccines is valued at approximately $1.1 billion. Projections indicate robust growth, with the market expected to reach $2.4 billion by 2034, driven by increasing awareness of preventive healthcare and advancements in vaccine technology. This represents a Compound Annual Growth Rate (CAGR) of around 8.2% from 2025 to 2034.
https://exactitudeconsultancy.com/reports/65956/meningitis-b-vaccine-market
Human Papillomavirus Vaccine Types 16 18 Market
The global market for Human Papillomavirus (HPV) vaccines, particularly those aimed at preventing types 16 and 18, is valued at approximately $3 billion. The market is projected to reach around $5 billion by 2034, reflecting heightened awareness of HPV-related health risks and increased vaccination initiatives worldwide.
https://exactitudeconsultancy.com/reports/65955/human-papillomavirus-vaccine-types-16-18-market
CONTACT: Irfan Tamboli (Head of Sales) Phone: + 1704 266 3234 Email: sales@exactitudeconsultancy.comSign in to access your portfolio
Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles
Business Upturn
2 hours ago
- Business Upturn
Nuvama initiates buy call on Hexaware Tech with Rs 950 target price, says growth and margins to outpace peers
By Markets Desk Published on August 21, 2025, 07:31 IST Nuvama has initiated coverage on Hexaware Technologies with a buy rating and a target price of ₹950, expecting the mid-cap IT services player to continue outgrowing and outperforming its large-cap peers. The brokerage highlighted Hexaware's current revenue base of USD 1.4 billion and market capitalisation of ₹438 billion, which it believes positions the company in a 'sweet spot' for accelerating growth. Nuvama said Hexaware's strong client relationships, presence across verticals and service lines, and robust cash flow profile provide confidence in sustained growth. Over the CY24–27 period, it forecasts revenue to grow at a compound annual rate of 11% in dollar terms, with margin expansion of 250 basis points driving EBIT and EPS growth of 19% and 18% respectively. At current levels, Hexaware trades at 28 times and 24 times estimated earnings for CY26 and CY27, broadly in line with mid-cap peers such as LTIMindtree and Mphasis. Nuvama believes this valuation is justified given the company's superior growth outlook and improving profitability. Disclaimer: The views and recommendations made in this article are those of Nuvama. This article does not constitute investment advice. Investors should consult their financial advisors before making any investment decisions. Ahmedabad Plane Crash Markets Desk at
Yahoo
3 hours ago
- Yahoo
Dollar drifts as investors ponder Fed independence ahead of Powell speech
By Ankur Banerjee SINGAPORE (Reuters) -The U.S. dollar drifted on Thursday as investors fretted about the Federal Reserve's independence after yet another attack from President Donald Trump ahead of remarks from Chair Jerome Powell later this week that could influence the outlook for rates. Trump called on Fed Governor Lisa Cook to resign on the basis of allegations made by one of his political allies about mortgages she holds in Michigan and Georgia, intensifying his effort to gain influence over the U.S. central bank. Cook said she had "no intention of being bullied to step down" from her position at the central bank. Trump has also told aides he is considering trying to fire Cook, the Wall Street Journal reported on Wednesday. "It has the potential to raise questions around the Fed's oversight and regulatory functions but it has little to no near-term monetary policy implications," said Prashant Newnaha, senior Asia-Pacific rates strategist at TD Securities. That explained the relatively muted reaction in the currency markets to the news as the dollar initially dipped on the news but was mostly calm into the Asian session. The Japanese yen held onto gains made in previous sessions and was little changed at 147.41 per dollar, while the euro was steady at $1.1642. Sterling last fetched $1.34535. That left the dollar index, which measures the U.S. currency against six other peers, steady at 98.301. Trump has repeatedly criticised Powell for being too slow to cut rates, stoking investor worries about the central bank's independence and its credibility. Investors expect Trump will replace Powell with a more dovish appointment when his term ends in May. Trump earlier this month said he would nominate Council of Economic Advisers Chairman Stephen Miran to serve out the final few months of a vacant Fed seat after Adriana Kugler unexpectedly resigned. Kristina Clifton, a senior economist at the Commonwealth Bank of Australia in Sydney, said if Cook resigns it would create another opening for Trump to appoint a Fed Governor who will vote to lower interest rates. "Perceived political interference in the Federal Reserve can undermine its independence, steepening the yield curve and denting the USD's safe haven status." POWELL SPEECH The main focus this week has been on whether Powell will push back against market expectations for a rate cut at the Fed's September 16-17 meeting when he speaks on Friday at the Jackson Hole meeting, following a weak jobs report for July. "Markets are adamant that recent labour market data necessitates some policy calibration and are expecting Chair Powell to tip his hat in that direction," TD's Newnaha said. Traders are pricing in an 82% chance of a 25-basis-point rate cut next month, CME FedWatch tool showed. While the odds have lowered from last week after hotter than expected producer price inflation tempered expectations, investors are still pricing in over 50 bps of easing this year. Some analysts cautioned that markets could end up being disappointed by Powell's speech, noting that the impact of Trump's tariffs on inflation remains uncertain. "It is not clear that Powell will deliver strong guidance," said Benoit Anne, managing director in the investment solutions group at MFS Investment Management. If the dovish signals elude us, there will be significant pricing out of the odds for a September cut." In other currencies, the New Zealand dollar was nursing steep overnight losses at $0.58205 after diving 1.2% to its lowest level since April. New Zealand's central bank cut interest rates on Wednesday as expected but left the door wide open to yet more easing if needed. The Australian dollar eased 0.13% to $0.64245, hovering near a two-week low. [AUD/]
Indianapolis Star
3 hours ago
- Indianapolis Star
A Drug that Could Reduce Metastatic Cancer Resurgence due to Its Anti-Inflammatory Effects in Viral Infections is in Clinical Trials
SHELTON, CONNECTICUT / ACCESS Newswire NanoViricides, Inc., a publicly traded company (NYSE American:NNVC) (the 'Company'), and a clinical stage, leading global pioneer in the development of broad-spectrum antivirals based on host-mimetic nanomedicine technology that viruses cannot escape, reports that its broad-spectrum antiviral drug NV-387 could help reduce resurgence of metastatic cancer caused by awakening of 'sleeping' cancer cells due to viral infections. NV-387 has successfully completed a Phase I clinical trial and is being advanced into Phase II clinical trials. Recently, increase in inflammation, and particularly the cytokine IL-6, caused by viral infections has been found to be linked to an increased risk of resurgence of metastatic cancer, in a study of COVID-19 (SARS-CoV-2 infection) and breast cancer, as well as Influenza virus infections and cancer [1] . This study has further substantiated that viral infections can lead to resurgence of metastatic cancers by re-activating 'sleeping' cancer cells. 'NV-387 is a remarkable antiviral drug, in that it not only attacks the virus, but also reduces inflammation, calming the human immune system so that untoward effects do not take place,' said Anil R. Diwan, Ph.D., President and Chairman of the Company, adding, 'We have found that NV-387 treatment reduces inflammation markers, particularly, IL-6, thereby protecting lungs. This reduction in inflammation and cyto-protective effect of NV-387 would also help minimize the risk of reawakening cancer, based on these reported studies.' Thus NV-387 treatment could have a strong impact in the treatment of cancer patients in remission who suffer from a viral infection that could lead to the cancer returning with metastasis to multiple sites in the body. COVID-19 has become endemic globally, with generally two waves every year. The summer surge is already occurring in the USA, with approximately 4,000 hospitalizations per week in the week ending July 26 at the beginning of the surge, fueled by ever-changing variants [2] . Influenza virus is a well-known endemic virus that causes pandemics globally. RSV is an endemic virus that causes particularly severe diseases in infants and children as well as adults. Measles virus causes 'immune system amnesia' and is increasing globally. NV-387 is the only antiviral drug that has been uniquely found to be effective in the treatment of lethal lung viral infections caused by all of these viruses in animal model studies that are predictive of human clinical effectiveness. This clearly demonstrates the unmet medical need for NV-387, a broad-spectrum antiviral that the viruses cannot escape even as new variants are created. In contrast, antibodies and vaccines readily fail with new variants arising, as is now well known. NV-387 treatment has been found to reduce the level of IL-6 in lethal viral infections causing lung diseases in animal models. Excellent protection of lungs was found to occur in NV-387-treated animals but not in ribavirin treated animals in a lethal RSV infection study. Strong protection of lungs was found to occur in NV-387-treated animals in a lethal lung-infection of Influenza A/H3N2 study. In this Influenza study, the approved drugs Tamiflu (oseltamivir), Rapivab (peramivib), and Xofluza (baloxavir) failed to protect the lungs of animals to any appreciable extent, indicating the superiority and clinical viability of NV-387. The Company further investigated the extra-ordinary effect of NV-387 on protection of lungs in lethal viral infections. Reduction in inflammatory cytokines, particularly IL-6, was found to occur to an appreciable extent in NV-387 treated animals. ABOUT NANOVIRICIDES NanoViricides, Inc. (the 'Company') ( is a publicly traded (NYSE-American, stock symbol NNVC) clinical stage company that is creating special purpose nanomaterials for antiviral therapy. The Company's novel nanoviricide™ class of drug candidates and the nanoviricide™ technology are based on intellectual property, technology and proprietary know-how of TheraCour Pharma, Inc. The Company has a Memorandum of Understanding with TheraCour for the development of drugs based on these technologies for all antiviral infections. The MoU does not include cancer and similar diseases that may have viral origin but require different kinds of treatments. The Company has obtained broad, exclusive, sub-licensable, field licenses to drugs developed in several licensed fields from TheraCour Pharma, Inc. The Company's business model is based on licensing technology from TheraCour Pharma Inc. for specific application verticals of specific viruses, as established at its foundation in 2005. Our lead drug candidate is NV-387, a broad-spectrum antiviral drug that we plan to develop as a treatment of RSV, COVID, Long COVID, Influenza, and other respiratory viral infections, as well as MPOX/Smallpox infections. Our other advanced drug candidate is NV-HHV-1 for the treatment of Shingles. The Company cannot project an exact date for filing an IND for any of its drugs because of dependence on a number of external collaborators and consultants. The Company is currently focused on advancing NV-387 into Phase II human clinical trials. The Company is also developing drugs against a number of viral diseases including oral and genital Herpes, viral diseases of the eye including EKC and herpes keratitis, H1N1 swine flu, H5N1 bird flu, seasonal Influenza, HIV, Hepatitis C, Rabies, Dengue fever, and Ebola virus, among others. NanoViricides' platform technology and programs are based on the TheraCour® nanomedicine technology of TheraCour, which TheraCour licenses from AllExcel. NanoViricides holds a worldwide exclusive perpetual license to this technology for several drugs with specific targeting mechanisms in perpetuity for the treatment of the following human viral diseases: Human Immunodeficiency Virus (HIV/AIDS), Hepatitis B Virus (HBV), Hepatitis C Virus (HCV), Rabies, Herpes Simplex Virus (HSV-1 and HSV-2), Varicella-Zoster Virus (VZV), Influenza and Asian Bird Flu Virus, Dengue viruses, Japanese Encephalitis virus, West Nile Virus, Ebola/Marburg viruses, and certain Coronaviruses. The Company intends to obtain a license for RSV, Poxviruses, and/or Enteroviruses if the initial research is successful. As is customary, the Company must state the risk factor that the path to typical drug development of any pharmaceutical product is extremely lengthy and requires substantial capital. As with any drug development efforts by any company, there can be no assurance at this time that any of the Company's pharmaceutical candidates would show sufficient effectiveness and safety for human clinical development. Further, there can be no assurance at this time that successful results against coronavirus in our lab will lead to successful clinical trials or a successful pharmaceutical product. This press release contains forward-looking statements that reflect the Company's current expectation regarding future events. Actual events could differ materially and substantially from those projected herein and depend on a number of factors. Certain statements in this release, and other written or oral statements made by NanoViricides, Inc. are 'forward-looking statements' within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934. You should not place undue reliance on forward-looking statements since they involve known and unknown risks, uncertainties and other factors which are, in some cases, beyond the Company's control and which could, and likely will, materially affect actual results, levels of activity, performance or achievements. The Company assumes no obligation to publicly update or revise these forward-looking statements for any reason, or to update the reasons actual results could differ materially from those anticipated in these forward-looking statements, even if new information becomes available in the future. Important factors that could cause actual results to differ materially from the company's expectations include, but are not limited to, those factors that are disclosed under the heading 'Risk Factors' and elsewhere in documents filed by the company from time to time with the United States Securities and Exchange Commission and other regulatory authorities. Although it is not possible to predict or identify all such factors, they may include the following: demonstration and proof of principle in preclinical trials that a nanoviricide is safe and effective; successful development of our product candidates; our ability to seek and obtain regulatory approvals, including with respect to the indications we are seeking; the successful commercialization of our product candidates; and market acceptance of our products. The phrases 'safety', 'effectiveness' and equivalent phrases as used in this press release refer to research findings including clinical trials as the customary research usage and do not indicate evaluation of safety or effectiveness by the US FDA. FDA refers to US Food and Drug Administration. IND application refers to 'Investigational New Drug' application. cGMP refers to current Good Manufacturing Practices. CMC refers to 'Chemistry, Manufacture, and Controls'. CHMP refers to the Committee for Medicinal Products for Human Use, which is the European Medicines Agency's (EMA) committee responsible for human medicines. API stands for 'Active Pharmaceutical Ingredient'. WHO is the World Health Organization. R&D refers to Research and Development. Public Relations Contact: ir@ [1] Publication: 'Respiratory viral infections awaken metastatic breast cancer cells in lungs', Chia et al, J DeGregori group, [2] Centers for Disease Control and Prevention. COVID Data Tracker. Atlanta, GA: U.S. Department of Health and Human Services, CDC; 2025, August 18. SOURCE: NanoViricides, Inc. View the original press release on ACCESS Newswire The post A Drug that Could Reduce Metastatic Cancer Resurgence due to Its Anti-Inflammatory Effects in Viral Infections is in Clinical Trials appeared first on DA80 Hub.
