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Zika Vaccines

Zika Virus Vaccine Candidates December 2025

Developing a safe and efficacious Zika vaccine and monoclonal antibody (mAb) is a global health priority, says the World Health Organization (WHO). However, as of December 2025, the U.S. Food and Drug Administration (FDA), Brazil, the European Medicines Agency (EMA), and the United Kingdom have not approved any Zika vaccine or mAb. A series of papers summarizes the key challenges and knowledge gaps that must be addressed to advance Zika vaccine research. As of 2025, a review identified 16 Zika vaccine candidates in Phase 1 or 2 trials, and three monoclonal antibodies (mAbs) were in Phase 1 trials. Zika vaccine clinical trials involving a DNA-based, modified vaccinia Ankara vector platform and purified inactivated vaccine candidates (January 2023May 2023October 2023) demonstrate that these vaccine candidates can induce Zika-neutralizing monoclonal antibodies.

Since 2016, approximately $350 million in research funding for a Zika vaccine has been mobilized (Chapman et al., 2020; U.K.'s Newton Fund, U.S. HHS). The U.S. National Institute of Allergy and Infectious Diseases (NIAID) is developing multiple vaccine candidates to prevent Zika infection.

France-based Valneva SE's VLA1601 is the most advanced Zika vaccine candidate. It is a second-generation, highly purified, inactivated, adjuvanted vaccine candidate adsorbed on aluminum hydroxide. On March 26, 2024, Valneva Austria GmbH announced the initiation of an additional two-dose, Phase 1 clinical trial (VLA1601-102), with initial results posted on November 4, 2025.

ZPIV is a Zika virus vaccine candidate with a purified, formalin-inactivated Zika virus. In June 2023, a study found that ZPIV was well tolerated in flavivirus-naïve and previously vaccinated adults; the immunogenicity of ZPIV in bats varied significantly by flavivirus vaccination status. Immune bias towards the flavivirus antigen of initial exposure and the timing of vaccination may have impacted responses. In this Phase 1 clinical trial, a third ZPIV dose significantly reduced, but did not eliminate, the immunogenicity discrepancy.

TAK-426 (PIZV) is a purified, inactivated, alum-adjuvanted, whole Zika virus vaccine candidate. It is being tested to provide safety and immunogenicity data for further clinical development.

Brazil-based Butantan Institute is developing a vaccine against the Zika virus. Animal tests are expected to begin in the second half of 2024.

iosBio OraPro-Zika is an orally administered Zika virus vaccine candidate based on a non-replicating human adenovirus type 5 (AdHu5) (E1/E3 deleted) expressing Zika transgenes.

GEO-ZM02 is constructed using a modified vaccinia Ankara vector platform. Preclinical studies demonstrated that a single dose of GEO-ZM02 provided 100% protection against the lethal Zika virus. This Zika vaccine is based on the virus's NS1 protein, which is not associated with the antibody-dependent enhancement of infection.

Ad26.ZIKV.001 is a replication-incompetent human adenovirus serotype 26 (ad26) vector vaccine candidate. In a clinical trial, researchers found that two doses of Ad26 were effective. ZIKV. 001 were safe, causing mild to moderate reactogenicity and inducing persistent neutralizing antibody responses. The single dose had lower peak antibody levels but was durable for a year. 

GeneOne Life Science and Inovio Pharmaceuticals' phase 1, open-label clinical trial of the DNA vaccine GLS-5700 elicited anti-ZIKV immune responses. 

VRC5283 is a Zika virus DNA vaccine candidate composed of a single closed-circular DNA plasmid encoded with wild-type precursor transmembrane M and envelope proteins from the H/PF/2013 strain of ZIKV. It is being tested in a phase 2 clinical study.

The University of Adelaide was awarded $1.35 million in funding to develop a novel DNA vaccine, pVAX-tpaNS1, for the treatment of the Zika virus. Dry-coating of pVAX-tpaNS1 on the HD-MAP device resulted in no loss of vaccine stability at 40°C storage over 28 days.

rZIKV/D4Δ30-713 is a live attenuated chimeric Zika candidate vaccine expressing the premembrane (prM) and envelope (E) genes of a contemporary ZIKV strain within a dengue DEN4Δ30 background. It completed a phase 1 clinical trial. The researchers wrote: Our results suggest rZIKV/DEN4Δ30 is over-attenuated and thus will not be further developed as a candidate ZIKV vaccine.

ZikaEnv:aghFc is a plant-based recombinant vaccine that transiently expresses the ZIKV envelope protein. At a low dose (1–5 μg), it induces humoral and cellular immunity.

Duke-NUS researchers used live-attenuated vaccine (ZIKV-LAV) strains of the Zika virus, which are weakened and have limited ability to infect healthy cells.

ZIKV E DIII-specific antibody ZK2B10, isolated from a ZIKV convalescent individual, is being developed by Uvax Bio.

Research suggests that the novel, auto-adjuvanted, virus-like particle technology EDIII-QβVLP vaccine is a promising candidate for preventing ZIKV infection, with potential applications in combating this and other emerging flaviviruses.

Zika Infection in Infants

On July 3, 2025, The Lancet published: A decade later, what have we learned from the Zika epidemic in children with intrauterine exposure? The Zika virus in pregnancy carries severe teratogenic potential to the fetus, ranging from congenital Zika syndrome to milder neurodevelopmental sequelae. Congenital Zika syndrome is associated with a spectrum of alterations that can affect cognitive, language, and motor development. The first human cases were detected in 1952. Since 2013, 31 countries and territories have reported cases of congenital microcephaly and other central nervous system malformations associated with Zika virus infection.

Zika and Dengue Co-Infections

A significant safety concern for vaccine development against ZIKV is the antibody-dependent enhancement of infection between ZIKV and the Dengue virus. Preexisting immunity to ZIKV has been recognized as a factor that can aggravate subsequent Dengue infection in animal models and humans. As of November 2025, Dengue vaccines are offered in various countries, but not in the United States. 

Zika Outbreaks

Zika outbreaks have been confirmed in numerous countries in 2025.

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Thursday, December 11, 2025 - 11:10
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Zika vaccine candidates are conducting clinical trials in 2025.
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Ambirix Hepatitis Vaccine

Ambirix Vaccine Description - 2022

Ambirix contains inactivated (killed) hepatitis A virus and ‘surface antigen’ (proteins from the surface) parts of the hepatitis B virus as active substances.

These vaccines are used to protect against the same diseases, but Twinrix Adult is given as a three-dose schedule, whereas Ambirix is given as 2 injections 6 to 12 months apart.

Protection against hepatitis B infections may not be obtained until after the second dose.

Ambirix is a registered trademark of the GlaxoSmithKline Group of Companies.

Ambirix Vaccine Indication

Ambirix is indicated in non-immune children and adolescents from 1 year up to and including 15 years of age for protection against hepatitis A and hepatitis B infection.

Ambirix should be used only when there is a relatively low risk of hepatitis B infection during the vaccination course.

Ambirix Vaccine Dosage

It is recommended that Ambirix be administered in settings where completion of the two-dose vaccination course can be assured. A dose of 1.0 ml is recommended for subjects from 1 year up to and including 15 years of age.

The standard primary course of vaccination consists of two doses, the first administered at the selected date and the second between 6 and 12 months after the first dose.

The recommended schedule should be adhered to. Once initiated, the vaccination's primary course should be completed with the same vaccine.

Vaccine Schedules for 2022

The CDC issues vaccine guidelines each year.  This year's recommended immunization schedules can be found here.

Ambirix Vaccine Clinical Studies

Three main studies of Ambirix were carried out in a total of 615 children from one year of age. All of the children received two doses of Ambirix six months apart. Two of the studies compared Ambirix with other vaccines against hepatitis A and B. The main measure of effectiveness was the proportion of vaccinated children who developed protective levels of antibodies one month after the last injection.

An additional study in 208 children compared the vaccine’s effectiveness when a six-month or a 12-month interval was used between the two injections.

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Travel Discounts

Travel Discounts December 2025

Vax-Before-Travel empowers travelers with information to have a healthy travel experience abroad while minimizing costs. Vaccine discounts are available for qualifying people from government agencies and commercial firms in 2025.

Lab Test Discounts

Lab testing discounts are offered by Ulta Labs Tests in 2025.

    Travel Insurance

    Get up to $5 million of travel medical insurance from Goose Insurance Services.

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    Cruise Ship Discounts

    Carnival Cruise Line offers 'last-minute' deals.

    Royal Caribbean offers 'quick-getaway' cruise discounts in 2025.

    Airport Lounge Travel Discounts

    Airport Lounges are among the most exclusive lounges in the American Express Global Lounge Collection.

    Priority Pass offers access to over 1,700 airport lounges, complimentary Food and Drinks, and Discounts on Airport Dining and Spa Treatments.

    Travel Credit Cards

    Turn your everyday purchases into more rewarding stays with the Hilton Honors American Express Cards.

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    Travel discounts include vaccines, lab tests, cruises, hotels, insurance

    Ad5-EBOV Ebola Vaccine

    CanSinoBio Ad5-EBOV Ebola Vaccine Description 2022

    CanSinBio Ad5-EBOV is an adenovirus type 5 recombinant vector-based Ebola virus disease vaccine that protects against Ebola by relying on the recombinant replication-defective human adenovirus type-5 vector immune response. In addition, ad5-EBOV is manufactured as a lyophilized powder, highly stable, and does not require storage at ultra-low temperatures. This feature renders it viable for use in resource-limited tropical areas.

    CanSino Biologics's Ad5-EBOV received NDA approval in China in October 2017. Ad5-EBOV has shown an acceptable stability profile and does not require ultra-low temperature storage conditions.

    In 2014, a single-center, double-blind, placebo-control, dose-escalation phase 1 clinical trial was performed in Taizhou, China. The findings showed that the Ad5-EBOV vaccine was safe and robustly immunogenic. In this add-in study, the investigators intended to evaluate the safety and immunogenicity of a booster dose of the recombinant Ebola adenovirus vector vaccine (Ad5-EBOV) in healthy adults after primary immunization. The investigators expect that boosting immunization with the same vaccine for primary immunization is possible and could confer longer-lived protection when needed.

    In July 2015, the First Affiliated Hospital of Zhejiang University launched a single-center, open, dose-escalation phase 1 clinical trial. This study will determine the safety and side-effect profile and immunogenicity of an investigational Ad5-EBOV vaccine in Healthy Adult Africans aged 18-60 years in China.

    CanSino Biologics Inc.'s Ad5-EBOV vaccine is currently in China's national stockpile. In addition, CanSinoBio announced its new brand identity on April 24, 2022.

    CanSinoBio Ad5-EBOV Ebola Vaccine Indication

    Ad5-EBOV is indicated to prevent an infection of the Ebola disease. One shot of the high dose vaccine could mount a glycoprotein-specific humoral and T-cell response against the Ebola virus in 14 days. In addition, the company says, 'As compared to competing products from multinational companies, our Ad5-EBOV has shown a better stability profile and does not require ultra-low temperature storage conditions.'

    CanSinoBio Ad5-EBOV Ebola Vaccine News 2014 - 2022

    April 23, 2022 - Bloomberg.com reported a man infected with Ebola disease died in the north western province of the DRC.

    August 12, 2020 - CanSino Biologics Inc. announced that it has successfully listed on the Sci-Tech Innovation Board (STAR Market) of the Shanghai Stock Exchange, making it the first "A+ H" dual listing vaccine company.

    October 24, 2017 - Ad5-EBOV, the recombinant adenovirus vector-based vaccine, is the first Ebola shot based on the strain behind the recent epidemic in West Africa in 2014—the deadliest outbreak in recorded history.

    October 14, 2014 - A Booster Dose of Ad5-EBOV in Healthy Adults After Primary Immunization.

    CanSinoBio Ad5-EBOV Ebola Vaccine Clinical Trials

    Yu Xuefeng, chairman and CEO of CanSinoBIO, points out that from a concept to an approved product, the development of the Ad5-EBOV vaccine took just a little more than three years, demonstrating CanSinoBIO’s strong capability for efficiently pushing a candidate through R&D and completing pre-clinical studies and clinical trials. 

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    Vitagerpavac Herpesvirus Vaccine

    Vitagerpavac Herpesvirus Vaccine Description

    Vitagerpavac is a multivalent vaccine for treating chronic herpesvirus infection (HCV) of types I and II. Vitagerpavac is a dry, inactivated herpes simplex virus (HSV) culture vaccine that has been obtained by using the Vero B continuous cell line as a substrate for the accumulation of herpes simplex virus types 1 (US strain) and 2 (VN strain).

    The vaccine stimulates body mechanisms of cellular resistance to herpes simplex virus type 1 and type 2. The tolerability and therapeutic effectiveness of the vaccine were tested in patients diagnosed as having chronic, frequently recurring herpes.

    The clinical trials have yielded positive results that suggest it is expedient to introduce the new Vitagerpavac into practice to treat chronic recurrent herpetic infection of various localizations. 

    The vaccine was developed at the Research Institute of Virology. DI. Ivanovsky RAMS and has been used in the Russian Federation for over 15 years. Approved by the Ministry of Health in the form of guidelines of the Russian Federation MR 3.3.1.0002-10 "Immunization with the" Vitagerpavac "vaccine. ATX codeJ07BX 

    JSC "FIRM" VITAFARMA ", 125124, Moscow, 1st street Yamskogo Polya ST. 17, building 15.  TEL: (499) 257-10-90

    Vitagerpavac Herpesvirus Vaccine Indication

    This Russian vaccine is indicated to prevent the chronic herpes virus infection of HSV1 and HSV2.  It is indicated for patients with a chronic herpes infection in remission.

    Contraindications for vaccination: active herpes infection (relapse), acute infectious and non-infectious diseases, chronic diseases in the acute stage, malignant neoplasms, pregnancy, and the presence of active symptoms of AIDS.

    Vitagerpavac Herpesvirus Vaccine Dosage

    The vaccination course includes 5 injections carried out at intervals of 7-10 days between injections.

    Vaccination is carried out in a medical institution under the supervision of medical staff. The vaccine is used during the remission stage, including ophthalmic herpes, not earlier than 10 days after the complete disappearance of the clinical manifestations of herpes infection. The vaccination course consists of 5 injections with an interval of 7 days, revaccination (repeated administration according to the same course of treatment) - after 6 months.

    If, after the 1st or subsequent injections, herpetic infection reoccurs, this means a case of pronounced immunosuppression. In such cases, vaccination should be temporarily discontinued, and anti-viral agents containing recombinant alpha-2 interferon (Genferon 500 000 IU suppositories) should be used to suppress the reoccurrence of herpes, 1 suppository 2 times a day for 5-10 days. Then, 10 days after the herpes rash or lesions disappear, the Vitagerpavac course of treatment should be restarted from the beginning.

    Coadministration of the Vitagerpavac vaccine and the immunomodulator Giaferon has been shown to have some advantage over the vaccination only. The new formulation of the agent as suppositories (per rectum) enhances the vaccine's immunogenicity and protective properties reducing the frequency of its application and making it more convenient for patients to use, says the company.

    Vitagerpavac Herpesvirus Vaccine Availability

    This vaccine has only been approved for use in Russia. According to this website, this product only ships in cold months, and the next scheduled shipment will be in October 2022.

    Vitagerpavac Herpesvirus Vaccine News

    September 2009 - Vitagerpavac is the first Russian herpes simplex virus vaccine obtained on the Vero B cell line.

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    Delta gD-2 (∆gD-2) Herpes Vaccine

    Delta gD-2 (∆gD-2) Herpes Vaccine Description 2022

    X-Vax Technology, Inc.'s Delta gD-2 (∆gD-2) herpes vaccine candidate is reported to elicit antibodies that facilitate the killing of infected cells, which then rapidly clears the HSV-1 HSV-2 viruses. X-Vax's approach eliminates the immunodominant protein found on the virus's surface that other researchers have focused on developing a reaction against. In addition, x-Vax believes that it would stimulate the body to produce different and more effective antibodies by deleting a gene from the virus.

    ∆gD-2 acts via a novel mechanism of action mediated by non-neutralizing, Fc receptor activating antibodies to prevent both HSV-1 and HSV-2 infection with a wide range of clinical and laboratory isolates. The vaccine induces Fc receptor activating antibodies that mediate antibody-dependent cellular cytotoxicity (ADCC) as the primary protection mechanism. ADCC is induced to flag infected cells for destruction by natural immune cells. The broad protection observed in various preclinical models combined with the potential for sterilizing immunity, as evidenced by the absence of latent virus, supports the clinical development of ∆gD-2, says X-Vax.

    'We have created a herpes vaccine candidate that we call ∆gD-2 (delta gD-2) because it is based on an HSV-2 virus genetically deleted for glycoprotein D (gD-2). With it, we have been able to prevent infections caused by herpes type 1 and type 2 in multiple preclinical models—with encouraging results,' says the company's website.

    X-Vax Technology, Inc. is a biotech company based in Jupiter, Florida, committed to developing vaccines against pathogens acquired by a mucosal infection such as herpes. "Our research leads us to believe that the new approach we are taking could succeed in defeating herpes." The company investors include but are not limited to Johnson & Johnson Innovation – JJDC, Inc. (JJDC); Adjuvant Capital, an impact investment fund supported by the Bill & Melinda Gates Foundation as an anchor investor; Serum Institute of India; Alexandria Venture Investments; and FF DSF VI, a scout investment vehicle out of Founders Fund. Company address: 3507 Kyoto Gardens Dr. Suite 310, Palm Beach Gardens, FL 33410.

    Delta gD-2 (∆gD-2) Indication

    The ∆gD-2 Herpes Vaccine candidate is indicated to clear the virus and prevent latency. Latency is a non-replicating state that periodically will reactivate, resulting in lifelong infection and the ongoing risk of shedding the virus to others.

    Delta gD-2 (∆gD-2) Clinical Development

    X-Vax pipeline states, 'we plan to gain commercial approval for the ∆gD-2 vaccine to prevent HSV type 1 and type 2. In addition, the potential for therapeutic application of the vaccine is under investigation.' 

    Extensive molecular and preclinical work has been completed for ∆gD-2, which induces unprecedented sterilizing immunity against both HSV-1 and HSV-2 challenge in multiple preclinical models. Not only did the vaccine prevent disease, but ∆gD-2 also prevented the virus from establishing latency, which no herpes vaccine has shown before. Latency refers to the ability of the herpes virus to remain dormant, particularly in nerve tissue, often establishing lifelong infection with frequent subclinical or clinical reactivation.

    Delta gD-2 (∆gD-2) News 2015 - 2022

    May 19, 2021 - Mark Terry with Biospace reported that X-Vax Technology is preparing to submit an Investigational New Drug Application to the U.S. Food and Drug Administration for its experimental vaccine against herpes simplex virus 1 and 2 (HSV-1 and -2). 

    November 6, 2020 - Study: The R2 non-neuroinvasive HSV-1 vaccine affords protection from genital HSV-2 infections in a guinea pig model.

    July 17, 2020 - Florida-based X-Vax Technology, Inc. announced Isaac Blech's appointment as Vice Chairman of the company's board of directors. As a co-founder of X-VAX, Mr. Blech previously served on the company's Board until December 2019.

    June 16, 2020 - A Single-Cycle Glycoprotein D Deletion Viral Vaccine Candidate, ΔgD-2, Elicits Polyfunctional Antibodies That Protect against Ocular Herpes Simplex Virus.

    October 10, 2019 - Murine Model of Maternal Immunization Demonstrates Protective Role for Antibodies That Mediate Antibody-Dependent Cellular Cytotoxicity in Protecting Neonates From Herpes Simplex Virus Type 1 & Type 2.

    October 3, 2019 - X-Vax believes the key to immunity against HSV is to prevent new virion production and release by killing infected cells. Its lead vaccine, ΔgD-2, elicits non-neutralizing antibodies that trigger antibody-dependent cellular cytotoxicity.

    July 23, 2019: Proceeds from the $56 million Series A financing will be used to advance X-VAX's lead program, a vaccine candidate against herpes called ∆gD-2 (delta gD-2), for further development and production, including a Phase 1 clinical study. "We believe that ∆gD-2 may be more promising than other previous vaccine candidates because it elicits a different type of immune response against HSV-1 and HSV-2 that is more effective in preclinical models at clearing virus and preventing the establishment of latency. In addition, in nonclinical models, immunization with ∆gD-2 elicits antibodies that facilitate the killing of infected cells, rapidly clearing the virus and thereby inducing sterilizing immunity," added William Jacobs, Ph.D., co-Inventor and Professor of Microbiology & Immunology at Albert Einstein College of Medicine.

    August 4, 2016 - Study published by JCI Insight: HSV-2 ΔgD elicits FcγR-effector antibodies that protect against clinical isolates - A single-cycle herpes simplex virus (HSV) deleted in glycoprotein D (ΔgD-2) elicited high titer HSV-specific antibodies (Abs) that (i) were rapidly transported into the vaginal mucosa; (ii) elicited antibody-dependent cell-mediated cytotoxicity but little neutralization; (iii) provided complete protection against lethal intravaginal challenge; and (iv) prevented the establishment of latency in mice. However, clinical isolates may differ antigenically and impact vaccine efficacy.

    May 10, 2015 - Research article: Herpes simplex type 2 virus deleted in glycoprotein D protects against vaginal, skin, and neural disease. 

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    IPOL Polio Vaccine

    IMOVAX Polio® Ipol® Vaccine 2025

    Sanofi Pasteur's single-antigen inactivated poliovirus vaccine (IPV), Imovax® (Ipol®), is highly purified, with enhanced potency, says the U.S. Food and Drug Administration (FDA). The IPOL is a sterile suspension consisting of three types of poliovirus that have been chemically killed: Type 1 (Mahoney), Type 2 (MEF-1), and Type 3 (Saukett). In addition, some combination vaccines (containing different vaccines in the same dose) include IPV, such as Pentacel (DTaP-IPV/Hib). IPV is also included in the children's vaccine series Pentacel and Quadracel.

    The U.S. Centers for Disease Control and Prevention's (CDC) Advisory Committee on Immunization Practices (ACIP) reviewed and voted on updated guidance for IPV vaccination on June 21, 2023. The ACIP reviewed a presentation on October 19, 2022, that confirmed IPV induces some nasopharyngeal mucosal immunity but limited intestinal immunity. However, IPV induces effective humoral immunity and prevents paralysis in approximately 90% of cases after two doses of the vaccine. Children in the USA should get an IPV to protect against poliomyelitis, according to the U.S. CDC's 2023 vaccination schedule. Additionally, the CDC recommends that children traveling to countries with a risk of contracting poliovirus complete the series before departure. Most adults do not need a polio vaccine booster because they received the vaccine as children, unless they are visiting areas with ongoing polio outbreaks.

    The WHO's Prequalification date was 09/12/2005. For more information, visit Sanofi Pasteur Vaccines.

    Fractional-Dose IPV

    The U.S. CDC says Fractional IPV (fIPV) is administered intradermally using one-fifth of the regular dose. The use of fIPV has been recommended by WHO as a response strategy for VDPV2 outbreaks. In July 2017, the WHO/PAHO published a Practical Guide to support countries in planning and implementing fIPV in the routine immunization schedule. Currently, fIPV is not recognized as a dose that satisfies immunization requirements in the U.S.

    IMOVAX IPOL Indication

    Polio immunization has been available in the United States since 1955 and has been part of the U.S. CDC's routine childhood immunization schedule for many decades. The IPOL vaccine is indicated for active immunization of infants (as young as six weeks), children, and adults to prevent poliomyelitis caused by poliovirus types 1, 2, and 3.

    IMOVAX IPOL Dosage

    IPOL is administered intramuscularly or subcutaneously. Single-antigen IPV is distributed in single-dose syringes or 10-dose vials. The recommended dose for both children and adults is 0.5 mL. It can be administered by the intramuscular or subcutaneous route, using a needle of an appropriate length for the age and size of the vaccine recipient.

    IMOVAX IPOL Active Substance

    IPOL Vaccine Active substance: Inactivated Poliovirus type 1 (Mahoney) 40D antigen units, Inactivated Poliovirus type 2 (MEF-1) 8D antigen units, Inactivated Poliovirus type 3 (Saukett) 32D antigen units.

    Poliomyelitis

    Poliomyelitis is a highly infectious disease caused by a virus that can invade the nervous system and cause total paralysis in hours. The virus enters the body through the mouth and replicates in the gastrointestinal tract, specifically in the intestine. Initial symptoms are fever, fatigue, headache, vomiting, neck stiffness, and limb pain. One in 200 infections leads to irreversible paralysis (usually in the legs). According to the World Health Organization, 5% to 10% of those paralyzed die when their breathing muscles become immobilized.

    IMOVAX IPOL Vaccine News

    June 9, 2025 - A Phase 3 Study - Safety and immunogenicity of a reduced-dose inactivated poliovirus vaccine versus a full-dose inactivated poliovirus vaccine in infants in Bangladesh, concluded that the Delivery of three intramuscular doses of the novel ds-IPV vaccine is safe and immunologically non-inferior to the Delivery of three intramuscular doses of IPV. The dose-sparing formulation may therefore become an attractive option for some national immunization programs due to lower expected vaccine costs.

    May 12, 2023 - The U.S. CDC reported that from January 1, 2021, to March 31, 2023, GPEI supported 48 countries in implementing 219 SIAs, during which approximately 988 million bOPV, 616,000 IPV, 960,000 fractional IPV, 90 million mOPV2, 595 million nOPV2, and 100 million tOPV doses were administered. 

    October 12, 2022 - The Lancet published an analysis that stated: Polio outbreak risk can be exacerbated in countries using inactivated polio vaccine, which offers excellent protection against paralysis but is less effective than an oral vaccine against poliovirus shedding, potentially allowing circulation without detection of paralytic cases

    October 5, 2022—Cattaraugus County, New York, Public Health Director Dr. Kevin D. Watkins is urging county residents who have not been vaccinated against polio to get vaccinated. Currently, polio cases are in upstate New York.

    September 28, 2022 - New York State Health Commissioner Dr. Mary T. Bassett declared poliovirus an imminent threat to public health in New York State, thereby expanding the availability of funding and resources to support local health departments in establishing immunization clinics, deploying vaccines to health care partners, and conducting outreach to unvaccinated and under-vaccinated New Yorkers to increase immunization rates, particularly in the areas affected by the virus and among children.

    September 28, 2022 - HEALTH ADVISORY: Update #3 Regarding Poliovirus in New York State. If an adult at risk has reason to believe they were not vaccinated. Records cannot be easily and quickly obtained, so they are treated as if they were not vaccinated. Additionally, all children and adolescents (up to 17 years of age) who are unvaccinated or under-vaccinated should be brought up to date with all routine CDC-recommended IPV doses. This is particularly urgent if they live, work, attend school, or have frequent social interactions with communities where poliovirus has been repeatedly detected in wastewater (currently Rockland, Orange, and Sullivan Counties).

    September 26, 2022 - Due to a recent confirmed poliovirus case in a neighboring state, the New Jersey Department of Health (NJDOH) requests that healthcare provider offices and pharmacies consider stocking IPV to increase access for people seeking vaccination.

    August 4, 2022: The New York State Department of Health stated, "This unprecedented circulation of polio in our community must be stopped. All unvaccinated children and adults should receive their first polio immunization immediately."

    April 26, 2022 - The rise of vaccine-derived polio cases has almost tripled from 2019 to 2020.

    March 27, 2022: The 'Two Drops' campaign will begin in Israel after health officials confirmed the first case of the potentially debilitating disease in the country in over thirty years.

    December 11, 2019 - FDA: Poliovirus Vaccine Inactivated (Monkey Kidney Cell). IPOL vaccine is indicated for active immunization of infants (as young as six weeks of age), children, and adults to prevent poliomyelitis caused by poliovirus types 1, 2, and 3.

    March 25, 2015: Sanofi Pasteur announced that the U.S. FDA has approved the use of Quadracel™ (Diphtheria and Tetanus Toxoids and Acellular Pertussis Absorbed and Inactivated Poliovirus; DTaP-IPV) vaccine for active immunization against diphtheria, tetanus, pertussis, and poliomyelitis in children 4 through 6 years of age.

    December 11, 1987 - Recommendations of the CDC Immunization Practices Advisory Committee Poliomyelitis Prevention: Enhanced-Potency Inactivated Poliomyelitis Vaccine -- Supplementary Statement.

    IMOVAX IPOL Clinical Trials

    IPOL has been tested in multiple clinical trials. Click here to review all the trials.

    The primary objective of this Phase III trial is to compare IMOVAX Polio to the current Chinese standard of care (OPV), which is administered over 2-3-4 months. The objective is to demonstrate that IMOVAX Polio is not inferior to OPV in seroprotection rates after the three-dose primary series. Additionally, the safety of IPV will be assessed after each dose of IPV.

    Clinical Safety Evaluation Phase 3 Study of the Sanofi Pasteur's Inactivated Poliomyelitis Vaccine (IMOVAX Polio™) Administered as a Single Booster Dose at 18 Months of Age in Healthy Chinese Children and as the First Dose of Primary Vaccination at 2 Months of Age in Healthy Chinese Infants.

    The primary objective of this Phase 2 study is to demonstrate the non-inferiority of fractional doses of IMOVAX Polio administered intradermally versus full doses of IMOVAX Polio administered intramuscularly in terms of seroprotection rates (polio types 1, 2, and 3) one month after the three-dose primary vaccination administered at 6, 10, and 14 weeks of age.

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    IPV
    Clinical Trial: 
    https://www.sanofi.com/en/science-and-innovation/clinical-trials-and-results/our-disclosure-commitments/pasteur
    Drug Class: 
    Inactivated Vaccine
    Condition: 
    Last Reviewed: 
    Wednesday, September 3, 2025 - 07:15
    Brand: 
    Imovax Polio®; Ipol®
    Status: 
    Manufacturer Country ID: 
    Kosher: 
    Yes
    Halal: 
    Yes
    Rate Vaccine: 
    pRKwzmy6

    MVA-BN RSV Vaccine

    MVA-BN® RSV Vaccine 2023

    Bavarian Nordic A/S's MVA-BN® RSV vaccine incorporates five different respiratory syncytial viruses (RSV) antigens to stimulate a broad immune response against both RSV subtypes (A and B), thus mimicking the immune response observed following a natural reaction to an RSV infection. The RSV vaccine candidate is based on Bavarian Nordic's proprietary MVA-BN® platform technology, also used in the Company's approved vaccines for smallpox and Ebola. 

    The U.S. Food and Drug Administration (FDA) granted Breakthrough Therapy Designation for MVA-BN® RSV targeting seniors 60 years and older. It has also been granted access by the European Medicines Agency (EMA) to its priority medicines (PRIME) scheme for MVA-BN® RSV in active immunization for the prevention of lower respiratory tract disease (LRTD) caused by RSV in adults ≥60 years of age.

    The peer-review Journal of Infectious Diseases published a Major Article on April 20, 2023, results from a phase 2a randomized double-blind, placebo-controlled clinical trial with adults that concluded MVA-BN-RSV vaccination resulted in lower viral load and symptom scores, fewer confirmed infections, and induced humoral and cellular responses.

    On July 22, 2023, Bavarian Nordic announced that its Phase 3 clinical trial of MVA-BN® RSV did not meet all the primary endpoints of preventing LRTD from RSV. The final study results showed that the vaccine candidate had a 59% efficacy in preventing at least two pre-defined LRTD symptoms meeting one of the efficacy criteria of the study. However, when measuring more severe LRTD based on at least three pre-defined symptoms, the vaccine candidate only demonstrated a 42.9% efficacy and missed the study's co-primary endpoint. Based on this outcome, Bavarian Nordic will discontinue its RSV program, including its partnership with Nuance Pharma to develop and launch the vaccine for selected Asian markets.

    Denmark-based Bavarian Nordic A/S (OMX: BAVA) is a fully integrated vaccines company focused on developing, manufacturing, and commercializing life-saving vaccines.

    Nuance Pharma Agreement in China

    In 2021, Nuance Pharma agreed with Bavarian Nordic, granting the Company exclusive rights to develop and commercialize MVA-BN RSV in the Chinese Mainland, Hong Kong, Macau, Taiwan, South Korea, and Southeast Asia addition on On November 13, 2022, the Company announced the Center for Drug Evaluation approved its Investigational New Drug application supporting its pivotal phase III clinical trial of the MVA-BN RSV vaccine against RSV in adults in mainland China. Founded by Mark Lotter in 2014, Nuance has built a late clinical-stage innovative portfolio.

    MVA-BN RSV Indication

    The MVA-BN-RSV Vaccine is indicated to prevent RSV, a highly infectious and the most common cause of lower respiratory tract infection in infants and children worldwide, resulting in many hospitalizations. RSV infections are also a serious health concern in the elderly and adults with cardiopulmonary disease. RSV is a common virus that usually causes mild, cold-like symptoms but, in serious cases, can cause severe lung infections, including bronchiolitis and pneumonia.

    According to the U.S. CDC, those at risk are typically young infants, the elderly, and people with weakened immune systems.

    MVA-BN RSV Side Effects

    No vaccine-related serious adverse events were observed in a recent phase 2 study. In addition, the vaccine was well-tolerated, consistent with the safety profile previously reported in phase 1 and phase 2 clinical studies announced by the Company.

    MVA-BN RSV Vaccine News 2023

    July 22, 2023 - "We are disappointed that our RSV vaccine candidate was unsuccessful in this pivotal trial," said Paul Chaplin, President and Chief Executive Officer of Bavarian Nordic. "While this outcome was unexpected and will impact our short-term growth expectations, we continue to have a unique commercial business, and given the recent strong brand and market growth, this provides a solid foundation for profitable growth in the years to come." 

    April 20, 2023 - A peer-review study concluded: The MVA-BN-RSV vaccine appears to represent a mode of action broader than other vaccine candidates focused on the production of neutralizing antibodies to the preF protein. Dependence of RSV vaccines on the activity of neutralizing antibodies against a specific epitope of one protein conformation may be risky, as such reliance may provide selective pressure for the development of mutant viruses capable of neutralizing antibody escape.

    April 11, 2023 - Bavarian Nordic A/S announced that the Phase 3 clinical trial of MVA-BN® RSV has accrued the number of cases required to complete the primary efficacy analysis, which is expected around mid-2023. Adjudicated data have confirmed enough patients with both 2+ symptoms and 3+ symptoms as required in the trial.

    December 22, 2022 - Bavarian Nordic A/S announced 20,000 adults aged 60 years and older had been enrolled in a phase 3 study. Topline results are anticipated in mid-2023.

    November 13, 2022 - "The MVA-BN RSV vaccine holds the potential to become the first to market adult RSV vaccine in China," in a press release, commented Mark G. Lotter, CEO and Co-Founder of Nuance Pharma.

    March 21, 2022 - Bavarian Nordic A/S announced an exclusive license and supply agreement with Nuance Pharma on the development and commercialization of MVA-BN® RSV against RSV in adults in the Chinese Mainland-Hong Kong, Macau, Taiwan, South Korea, and certain Southeast Asian countries.

    February 14, 2022 - The Company announced that the U.S. FDA had granted Breakthrough Therapy Designation for MVA-BN RSV for active immunization to prevent lower respiratory tract disease caused by RSV in adults aged 60 years or older. 

    September 1, 2021 - Bavarian Nordic A/S announced results from a human challenge trial of MVA-BN® RSV. The study demonstrated a significant reduction in viral load in vaccinated subjects (n=30) versus placebo (n=31), thus meeting the primary endpoint of this pivotal study. At the same time, the vaccinated subjects showed a significant reduction in clinical symptoms typically associated with RSV infections. As a result, the MVA-BN RSV vaccine demonstrated an efficacy of up to 79% in preventing symptomatic RSV infections.

    August 8, 2018: Bavarian Nordic announced positive data from the extension study of its Phase 2 study investigating the safety and immune responses of its universal RSV vaccine, MVA-BN® RSV, in an older adult population. 

    September 29, 2016: Bavarian Nordic announced the presentation of data from a Phase 1 study of its novel, broad-spectrum RSV (respiratory syncytial virus) vaccine candidate, MVA-BN RSV®.

    MVA-BN RSV Clinical Trials

    The Company developed a Phase 3 program. The global, randomized, placebo-controlled, double-blind Phase 3 VANIR clinical trial has enrolled more than 20,000 participants across more than 100 centers in the U.S. and Germany. The study's primary objective will assess the vaccine candidate's efficacy against LTRD caused by RSV. The trial is designed to run through the RSV season 2022/2023, with topline results expected mid-2023 if the pre-defined number of lower-respiratory tract disease events has occurred.

    Phase 2a Randomised, Double-Blinded, Placebo-Controlled Study to Assess the Safety, Immunogenicity, and Efficacy of the Recombinant MVA-BN® RSV Vaccine Against Respiratory Syncytial Virus Infection in the Virus Challenge Model in Healthy Adult Participants. Clinical Trial NCT02873286:  After receiving MVA-BN-RSV or placebo, 31 and 32 participants, respectively, were challenged. Viral load areas under the curve from nasal washes were lower (p = 0.017) for MVA-BN-RSV (median = 0.00) than placebo (median = 49.05). Total symptom scores also were lower (median = 2.50 and 27.00, respectively; p = 0.004). Vaccine efficacy against symptomatic, laboratory-confirmed, or culture-confirmed infection was 79.3% to 88.5% (p = 0.022 and 0.013). Serum immunoglobulin A and G titers increased ∼4-fold after MVA-BN-RSV vaccination. Interferon-γ-producing cells increased 4- to 6-fold after MVA-BN-RSV in response to stimulation with the encoded RSV internal antigens. Injection site pain occurred more frequently with MVA-BN-RSV. No serious adverse events were attributed to vaccination.

    0 min read
    Clinical Trial: 
    https://www.bavarian-nordic.com/what-we-do/resources/clinical-trials.aspx
    Drug Class: 
    Vaccine
    Last Reviewed: 
    Monday, July 24, 2023 - 06:45
    Brand: 
    MVA-BN® RSV
    Status: 
    Manufacturer Country ID: 

    Flublok Influenza Vaccine

    FluBlok® Vaccine Clinical Trials, Dosage, Indication, Side Effects

    Sanofi Flublok® is a recombinant influenza vaccine produced without using eggs. It, therefore, is not subject to the mutations that are sometimes introduced into the vaccine during the process of egg adaptation that can cause the traditional vaccines to be ineffective. Flublok was initially licensed (STN: 125285) for use in the USA by the Food and Drug Administration (FDA) in 2013 and the European Medicines Agency (EMA, EMEA/H/C/005159). It has been used since 2016 and distributed to over 9 million people. The FDA considers the vaccine safe and acceptable for use. Unlike other flu vaccines, Flublok is highly purified and does not contain influenza virus, antibiotics, formaldehyde, preservatives, egg protein, latex, gluten, or gelatin. Flublok Quadrivalent is given to people 18 years of age and older.

    On December 14, 2023, an Original Article published by the NEJM reported that the high-dose recombinant vaccine FluBlok conferred more protection against PCR-confirmed influenza than an egg-based standard-dose vaccine among adults between the ages of 50 and 64.

    FluBlok quadrivalent is marketed in the E.U. as Supemtek. The European Commission authorized it on November 18, 2020. Visit SanofiFluShots.com to learn about potential flu complications, including heart attack, stroke, and pneumonia, and more about Sanofi's Flublok Quadrivalent (Influenza Vaccine). 

    Sanofi is located at 14 Espace Henry Vallée, 69007 Lyon, France.

    FluBlok Vaccine Price

    Sanofi provides a guide for coding and reimbursement for vaccines. According to CMS.gov, the payment allowance for FluBlok in 2022-2023 is $69.94.

    FluBlok Vaccine Indication

    Flublok vaccine is given to people 18 years and older. Flublok should not be given to anyone with a severe allergic reaction (anaphylaxis) to any vaccine component (including eggs or egg products for Fluzone High-Dose Quadrivalent).

    On October 16, 2024, the U.S. FDA updated the label for FLUBLOK to include data from a new safety study involving pregnant women 18 years and older. In this study, FLUBLOK demonstrated no increased risk of pregnancy, birth, or neonatal/infant outcomes compared to a standard-dose flu vaccine and estimated pregnancy outcomes for the general population. Recombinant or inactivated flu vaccines are recommended by the U.S. CDC, Advisory Committee on Immunization Practices, and American College of Obstetricians and Gynecologists for individuals who are or will become pregnant during flu season.

    FluBlok and COVID-19 Vaccines

    The US Centers for Disease Control and Prevention (CDC) issued interim clinical considerations stating that 'COVID-19 vaccines and other vaccines, including influenza vaccines, can be administered without regard to timing.

    FluBlok Vaccine Dosage

    Administer Flublok Quadrivalent as a single 0.5 mL dose intramuscular injection only.

    FluBlok Vaccine News

    October 16, 2024 - Thomas Grenier, Head of Vaccines, North America, Sanofi, stated, "Today, we're proud to announce an important update to our label for FLUBLOK, from one of Sanofi's largest flu vaccine safety studies ever done in pregnant women, an important at-risk population group for influenza."

    September 13, 2023 - "The flu can be a serious public health threat, leading to complications such as heart attack, stroke, and pneumonia. These can be especially dangerous for older adults, ethnic and racial minority groups who are at an increased risk for being hospitalized from the flu, and those living with chronic conditions, like asthma, diabetes, and heart disease," commented Michael Greenberg, MD, MPH, North America Medical Head of Vaccines at Sanofi.

    August 26, 2022 - Sanofi's Flublok® Quadrivalent Vaccine was among the flu vaccines preferentially recommended by the U.S. CDC's ACIP for adults 65+.

    October 22, 2020 - Flublok has been given authorization for temporary supply by the U.K. Department of Health and Social Care and the Medicines and Healthcare products Regulatory Agency (MHRA) for immunization against flu in this year's seasonal flu program to meet public health needs. Their assessment was partly based on evidence from another closely related Sanofi flu vaccine, Supemtek. This was recommended for approval by the European Medicines Agency in September 2020. The MHRA assessment showed that the two products are fundamentally similar based on a review of the manufacturing, control, quality, non-clinical, and clinical evaluations.

    FluBlok Vaccine Clinical Trials

    As of October 2024, the Flublok vaccine has been studied in various clinical trials.

    The results from the study of more than 48,000 pregnant individuals across multiple flu seasons were recently published in the American Journal of Obstetricians and Gynecologists (AJOG) Global Reports. They demonstrate that FLUBLOK safety is consistent with a standard-dose flu vaccine and pregnancy-related outcomes in the general population.

    A phase 3 efficacy trial demonstrated improved protection against influenza compared to a standard-dose influenza vaccine and reduced the risk of flu by an additional 30% in adults aged 50 years and older.

    0 min read
    Availability: 
    Worldwide
    Generic: 
    Influenza Vaccine
    Drug Class: 
    Vaccine
    Condition: 
    Last Reviewed: 
    Thursday, October 17, 2024 - 10:55
    Brand: 
    FluBlok, Supemtek
    Status: 
    Manufacturer Country ID: 
    Rate Vaccine: 
    t0CeuQ0E

    EpiVacCorona Vaccine

    EpiVacCorona (Aurora-CoV) Vaccine Description

    EpiVacCorona (Aurora-CoV) is a COVID-19 preventive vaccine developed by the Vektor State Research Center of Virology and Biotechnology in Russia. EpiVacCorona is an antigens-based vaccine that provokes an immune reaction against COVID-19 and promotes immunity development. The EpiVacCorona vaccine contributes to developing protective immunity against SARS-CoV-2 coronavirus following two intramuscular administrations spaced 21-28 days apart.

    The EpiVacCorona vaccine relies on chemically synthesized peptide antigens of SARS-CoV-2 proteins, conjugated to a carrier protein and adsorbed on an aluminum-containing adjuvant (aluminum hydroxide). The vaccine does not contain the live virus and forms immunity due to artificially synthesized peptides.

    According to researchers, the peptides and the viral part of the chimeric protein should immunize people who received this vaccine against the SARS-CoV-2 coronavirus and trigger the production of protective antibodies.

    On October 14, 2020, Tatyana Alekseevna Golikova stated, 'I want to note that one hundred volunteers' clinical studies were carried out. Unlike the first Russian vaccine, "Sputnik V," which is a vector vaccine that is, produced based on adenovirus, the new vaccine was created based on one of the promising synthetic platforms, and it is a peptide vaccine; it consists of artificially synthesized short fragments of viral proteins - peptides, through which the immune system learns and subsequently recognizes and neutralizes the virus. I must say that the vaccine is characterized by the absence of reactogenicity and a sufficiently high level of safety.'

    The vaccine was licensed in Russia by State Virology and Biotechnology Center on October 14, 2020, and patented on December 7, 2020.

    A study published in 2021 stated, 'the vaccine (EpiVacCorona) is a suspension for intramuscular administration containing a composition of chemically synthesized peptide immunogens of the S protein of the SARS-CoV-2 coronavirus conjugated to a carrier protein and adsorbed on aluminum hydroxide.'

    On June 28, 2021, the CEO of the State Research Center of Virology and Biotechnology Vector, Rinat Maksyutov, said there were no fundamental distinctions between EpiVacCorona-N and the previous version of EpiVacCorona. "The vaccines are different from the standpoint of manufacturing techniques. This is precisely the main reason why more clinical tests had to be carried out. To achieve largescale production, not hundreds of thousands, but millions of the vaccine doses, certain manufacturing problems had to be addressed, and this required some amendments," as reported by TASS.

    Drugbank Accession Number: DB16439. Vaccine available as of Feb. 28, 2022, was in four countries.

    Federal Budgetary Institution of Science The State Research Center for Virology and Biotechnology "Vector" is one of Russia's largest scientific virological and biotechnological centers. The Center was organized in 1974. It includes a branch - the Institute of Medical Biotechnology, located in Berdsk, Novosibirsk Region.

    EpiVacCorona (Aurora-CoV) Vaccine Indication

    EpiVacCorona Vaccine is indicated to prevent COVID-19, a disease caused by SARS-Cov-2. The composition, dose, and administration of the future vaccine will be determined.

    Pregnant women and children will not participate in post-registration trials of a vaccine against the coronavirus developed by the Vector State Research Center of Virology and Biotechnology, the Federal Service for Surveillance press service on Consumer Rights Protection Human Wellbeing told TASS on October 2, 2020.

    EpiVacCorona Children

    As of September 2, 2021, no date has been announced for the start of clinical trials of the EpiVacCorona COVID-19 vaccine in children, reported TASS.

    EpiVacCorona Price

    TASS reported on May 15, 2021, the Industry and Trade Ministry stated that vaccines are being purchased under the price established by the Federal Antimonopoly Service based on the production capacities of the facility that produces them. According to TASS, the maximum purchase price of the EpiVacCorona vaccine is 842 rubles (US$11).

    EpiVacCorona-N Vaccine (AURORA-Covid-19)

    On August 26, 2021, local media reported the Russian Health Ministry registered the EpiVacCorona-N coronavirus vaccine. EpiVacCorona-N was developed by the Vector Center of Russian public health and Rospotrebnadzor. EpiVacCorona-N is now the fifth coronavirus vaccine registered in Russia. The vaccine can reduce the risk of contracting the novel coronavirus infection in adults aged 18 to 60 and shall be administered twice, with each shot 14 days apart.

    According to the information, the vaccine will be manufactured at Vector-BiAlgam, Geropharm, and the Vector Center.

    The Federal Service for Intellectual Property (Rospatent) registered the AURORA-CoV trademark on July 5, 2021, as a brand name for marketing the EpiVacCorona-N vaccine.

    EpiVacCorona Vaccine News

    March 24, 2022 - Reporting and data sharing level for COVID-19 vaccine trials: A cross-sectional clinical study. We recommend establishing a comprehensive, accurate data-sharing system for future vaccine trials.

    January 25, 2022 - The Ministry of Health explained why it suspended the purchase of EpiVacKorona.

    January 24, 2022 - Local media reported the Roszdravnadzor drug distribution database indicates the EpiVacCorona and Epivaccorona-H vaccines have not been distributed in 2022. 

    December 28, 2021 - TASS reported over 85% of Russian athletes bound for the 2022 Winter Olympic Games in China had been vaccinated against COVID-19.

    December 17, 2021 - TASS reported the first 12,000 doses of the EpiVacCorona-N vaccine had been released. The batch will be used for the third phase of clinical trials.

    November 26, 2021 - TASS reported Russia plans to supply EpiVacCorona vaccines to Kazakhstan.

    October 15, 2021 - ANI reported Russia will provide EpiVacCorona vaccines to Venezuela.

    October 4, 2021 - TASS reported athletes inoculated with Russian-made anti-COVID-19 vaccines will be allowed to participate in the 2022 Winter Olympic Games in Beijing, China.

    September 22, 2021 - Anna Popova, the Head of the Federal Service for Surveillance on Consumer Rights Protection and Human Wellbeing, announced "Today, almost 40 mln adults have been fully inoculated against COVID-19 in Russia," Popova told the NTV channel.

    August 26, 2021 - Interfax reported EpiVacCorona-N is now the fifth coronavirus vaccine registered in Russia. EpiVacCorona-N was developed by the Vector Center of Russian public health and consumer protection watchdog Rospotrebnadzor. The vaccine can be used to reduce the risk of contracting the novel coronavirus infection in adults aged from 18 to 60 and shall be administered twice, with each shot 14 days apart, according to the vaccine's manual.

    August 14, 2021 - TASS reported no deaths related to the EpiVacCorona anti-coronavirus vaccine that had been registered in Russia, the Vektor Center told TASS.

    August 5, 2021 - TASS reported the efficacy of the EpivacCorona vaccine, according to the provisional results documented in the quality control review of the third phase of the vaccine's clinical trials, is 79%, citing Clinical Research Laboratory, an independent research organization.

    July 3, 2021 - Tass reported EpiVacCorona to be tested on teens when adult trials are over, and the developers see no need to modify the vaccine for children and teenagers.

    July 2, 2021 - TASS reported that more than 3.4 million doses of the anti-COVID vaccine EpiVacCorona had been manufactured in Russia, and more than 3.1 million doses have been released to use Virology and Biotechnology Vector under the consumer rights watchdog Rospotrebnadzor told the media.

    July 1, 2021 - Moscow Mayor Sergei Sobyanin announced a booster vaccine campaign across the capital. Sobyanin said revaccination was available with any of the four Russian-registered vaccines.

    June 28, 2021 - TASS reported an application for registering the anti-COVID vaccine EpiVacCorona-N submitted to the Russian Health Ministry. Earlier, the CEO of the State Research Center of Virology and Biotechnology Vector, Rinat Maksyutov, said there were no fundamental distinctions between EpiVacCorona-N and the previous version EpiVacCorona.

    June 24, 2021 - The EpiVacCorona vaccine is effective against the Delta and Delta Plus SARS-CoV-2 coronavirus strains, stated head of the Vector State Research Center of Virology and Biotechnology Rinat Maksyutov, reported TASS.

    June 17, 2021 - Local media reported the Russian Vector Research Center had started clinical trials of a three-dose regimen of its EpiVacCorona vaccine against COVID-19 on a group of volunteers, with the first results expected by Fall 2021.

    June 10, 2021 - TASS reported the production volumes of the EpiVacCorona vaccine are not yet sufficient to satisfy requests from abroad. Still, the applications can be satisfied at the end of the year, Industry and Trade Minister Denis Manturov said.

    June 4, 2021 - Venezuela agreed to purchase and manufacture doses of the EpiVacCorona vaccine. Geropharm director Pyotr Rodionov and Venezuelan Health Minister Carlos Alvarado signed the agreement, while Russian Minister of Industry and Trade Denis Manturov attended the event. Vaccine shipments are planned to begin in September 2021.

    June 2, 2021 - TASS reported the EpiVacCorona vaccine is expected to provide immunity from the COVID-19 for one year, according to Director General Rinat Maksyutov.

    May 14, 2021 - TASS reported Moscow residents might get inoculated against the coronavirus infection with the Sputnik V jab and the EpiVacCorona vaccine, Deputy Moscow Mayor Anastasia Rakov.

    April 28, 2021 - TASS reported 1,833,230 doses of the EpiVacCorona vaccine had been produced, and 1,271,560 doses have gone into civil circulation.

    April 9, 2021 - TASS reported the Russian Health Ministry had issued a permit to conduct Phase One and Two clinical trials of the EpiVacCorona-N vaccine against the coronavirus developed by the Vector State Research Center according to the Ministry's state registry of trial permits. Volunteers aged 18 to 60 will participate in the trials, the entry stated. The trials will involve 300 volunteers and will be conducted at the Federal Medical Biological Agency's medical facility in the Novosibirsk Region, beginning in April 2021, the completion - September 30, 2021.

    April 9, 2021 - Science Magazine published an article: Latest Russian vaccine comes with a big dose of mystery.

    April 6, 2021 - ScienceMag.org article wrote: 'no peptide-based vaccines have been licensed to date by the United States, Europe, or the World Health Organization (WHO). "There are several in clinical trials. This means we don't have definitive evidence they are effective, but they do look promising," says Sarah Caddy of the Cambridge Institute for Therapeutic Immunology and Infectious Disease.'

    April 5, 2021 - TASS reported about 230,000 sets of the EpiVacCorona vaccine by the Vector State Research Center of Virology and Biotechnology had been shipped to 40 Russian regions, the press service of the Federal Service for Surveillance on Consumer Rights Protection and Human Wellbeing reported.

    March 30, 2021 - Reuters reported Russia supplied Venezuela with 115,000 doses of EpiVacCorona vaccine to be used as part of the Russian coronavirus vaccine candidate's trials.

    March 30, 2021 -  TASS reported around 200,000 doses of the EpiVacCorona coronavirus vaccine had been made available for general use in Russia, deputy head of the vaccine developer, Vector Center, Tatyana Nepomnyashchikh, confirmed.

    March 25, 2021 - TASS reported Russia's EpiVacCorona coronavirus vaccine is safe and effective, according to the results of clinical trials on volunteers aged between 18 and 60 published in the Infection and Immunity journal, the Federal Service for Surveillance on Consumer Rights Protection and Human Wellbeing said in a statement.

    March 22, 2021 - Meduza journalists Svetlana Reiter and Alexander Ershov asked the main questions about EpiVacCoron to its developer Alexander Ryzhikov and Deputy Director-General of the Vector Center Tatiana Nepomnyashikh.

    March 22, 2021 - Reuters reported Russian scientists said the EpiVacCorona vaccine was effective against variants of the coronavirus.

    March 12, 2021 - It takes people inoculated with EpiVacCorona vaccine 42 days to develop immunity, according to the head of the Federal Service for Surveillance on Consumer Rights Protection and Human Wellbeing, Dr. Anna Popova, reported TASS. Popova says EpiVacCorona produces "quite strong and effective immunity" but works "rather slowly."

    March 5, 2021 - TASS reported inoculations with the EpiVacCorona vaccine developed by Russia's State Research Center of Virology and Biotechnology Vector would begin in the second half of March 2021, the center's Director-General Rinat Maksyutov told Vesti news.

    February 18, 2021 - TASS reported that all volunteers aged 18 to 60 had generated antibodies to COVID-19. However, Ryzhikov noted that the immunological efficacy in the volunteers aged over 60 was slightly lower and amounted to 94%. "It's an excellent result for this age," the expert concluded.

    February 16, 2021 - TASS reported experts of the Vector State Research Center of Virology and Biotechnology had confirmed the efficacy of Russian anti-coronavirus vaccines Sputnik V and EpiVacCorona against the virus' British strain. "The protective effect was demonstrated in neutralization reactions with the use of serum from people inoculated with the Sputnik V and EpiVacCorona vaccines, which contain antibodies to the SARS-CoV-2 virus," it said.

    February 3, 2021 - Local media reported Russia delivered the new coronavirus vaccine, EpiVacCorona, to Belarus, Head of the Federal Service for Surveillance on Consumer Rights Protection and Human Well-Being [Rospotrebnadzor] Anna Popova told reporters following her meeting with Belarusian Prime Minister Roman Golovchenko, BelTA has learned. Belarus' Healthcare Minister Dmitry Pinevich spoke highly of the new Russian vaccine. "We certainly hope that this vaccine will be supplied in larger quantities and that it will be highly instrumental in our efforts to combat the coronavirus."

    January 22, 2021 -  TASS reported the immune response to novel coronavirus is not developed earlier than 32-45 days after the vaccination, or 52 days later maximum, said Alexander Gorelov, the deputy director for science of the Central Research Institute of Epidemiology at the Russian Federal Service for Surveillance on Consumer Rights Protection and Human Wellbeing. On January 18th, Russian residents were informed they could receive one of the two registered vaccines Sputnik V or EpiVacCorona, for free.

    January 19, 2021 - Russia's Second COVID-19 Vaccine EpiVacCorona' 100% Effective' In Early Trials, according to the Russian local media outlet. The data based on Phase I and II trials were released before starting the Phase III trial. "The effectiveness of the vaccine is made up of its immunological effectiveness and preventative effectiveness," the TASS news agency reported, citing Rospotrebnadzor.

    January 18, 2021 - TASS reported mass production of the experimental Epivaccorona vaccine would be launched in February 2021, according to comments by Russian Deputy Prime Minister Tatiana Golikova.

    January 18, 2021 - TASS reported that Russians who were willing to be vaccinated could choose between two COVID-19 vaccines, Sputnik V and EpiVacCorona, registered in Russia. The Sputnik V vaccine was developed by the Gamaleya Scientific Research Institute of Epidemiology and Microbiology, and EpiVacCorona was created by the Research Center of Virology and Biotechnology Vector.

    December 30, 2020 - EpiVacCorona, Russia's potential COVID-19 vaccine, does not harm the embryo's health, the national consumer rights watchdog, Rospotrebnadzor, based on a pre-clinical, non-human study. "Based on the data obtained, it concluded that the EpiVacCorona vaccine does not have embryotoxic properties and does not affect the generative function," Rospotrebnadzor said. The watchdog added that the vaccine did not affect the offspring's survival rate and did not cause any disturbances in their physical development.

    December 25, 2020 - Media reported Russian regions received over 7,000 doses of the EpiVacCorona vaccine. And by the end of 2020, this amount will rise to over 14,000 doses, and by February, medical organizations should receive over 50,000 doses of the preparation, Russian Prime Minister Mikhail Mishustin said.

    December 15, 2020 - Over 1,400 volunteers get Russia's first EpiVacCorona vaccine jab. As many as 1,316 volunteers over the age of 18 and 122 volunteers over the age of 60 have received the first shot of Russia's EpiVacCorona coronavirus vaccine as part of post-registration trials Service for Surveillance on Consumer Rights Protection, and Human Wellbeing said in a statement on Tuesday.

    December 9, 2020 -  Documents related to the EpiVacCorona coronavirus vaccine developed by the Vector Center of the Federal Service for Surveillance on Consumer Rights Protection and Human Wellbeing (Rospotrebnadzor) have been submitted to the World Health Organization, Rospotrebnadzor head, and Russian chief public health official Anna Popova said.

    November 24, 2020 - Russia's EpiVacCorona vaccine developed by the Vector Center has been received by nine medical organizations for post-registration clinical trials. Two clinical trials are scheduled; the first will involve 150 people aged over 60, and the second will see 3,000 volunteers 18 years, and older get the vaccine. Five volunteers over 60 were inoculated on November 23, 2020.

    October 27, 2020 - Output of the vaccine developed by former biological weapons lab Vector State Virology and Biotechnology Center in Novosibirsk will ramp up by the end of the year, Anna Popova, the head of Russia's public-health watchdog, said at a conference.

    October 20, 2020 - Director-General Rinat Maksyutov told a virtual conference: "The expected advantage of this vaccine compared to other vaccine platforms is the effectiveness of the vaccine against antigenically evolving strains since the vaccine contains conservative SARS-COV-2 epitopes, the safety of the vaccine, … simplicity of production and stability of the components, as well as the mode of storage and transportation."

    October 14, 2020 - The Russian Federation President announced the 'Novosibirsk center "Vector" has registered the 2nd Russian vaccine against coronavirus "EpiVacCorona.'

    October 5, 2020 - Nearly 30,000 volunteers will participate in post-registration trials of the coronavirus vaccine developed by Russia's Vector State Research Center of Virology and Biotechnology, the Federal Service's press service for Surveillance on Consumer Rights Protection and Human Wellbeing told TASS.

    October 2, 2020 - Post-registration trials of a vaccine against the coronavirus developed by the Vector State Research Center of Virology and Biotechnology will begin in November-December 2020.

    September 30, 2020 - Experts from the Federal Institute of Industrial Property (FIPS) have completed the second examination phase related to the medicines from coronavirus infection SARS-Cov-2. The State Scientific Center of Virology and Biotechnology "Vector," located in Novosibirsk, has received patents for the vaccine from COVID-19.

    August 17, 2020 - The Vector State Research Center of Virology and Biotechnology in Novosibirsk has started the second phase of clinical studies of the vaccine against the novel coronavirus.

    August 6, 2020 - Another 86 volunteers will be inoculated with the vaccine against the novel coronavirus developed by the Vektor State Research Center of Virology and Biotechnology during the second stage of clinical trials, the press service of the Federal Service for Surveillance on Consumer Rights Protection and Human Wellbeing told TASS.

    August 5, 2020 - EpiVacCorona is being developed by VECTOR, taking into account all mandatory requirements and regulatory recommendations provided by the Russian Federation's legislation, the watchdog said. According to Rospotrebnadzor, the research protocols that comply with the Russian and world experience and strictly adhere to the research rules indicate the drug's quality.

    August 2, 2020 - "All vaccinated volunteers are in good health. No complications after the inoculation with the EpiVacCorona vaccine against the coronavirus have been recorded," the statement said.

    July 30, 2020 - The Russian Vektor State Research Center will monitor volunteers testing a vaccine against COVID-19 from three to six weeks. The official government site stop coronavirus. rf's Telegram channel, citing Russia's Rospotrebnadzor, a consumer watchdog.

    July 28, 2020 - Center "Vector" began testing the Russian peptide vaccine against COVID-19 disease.

    March 20, 2020 - In Russia, vaccine prototypes based on six different technological platforms for the prevention and control of the COVID-19 epidemic in the State Research Center of VB "Vector" of Rospotrebnadzor were developed in the shortest possible time.

    EpiVacCorona-N Vaccine Clinical Trials

    On October 13, 2020, a government statement indicated 'Vector will begin post-registration clinical trials in various Russian regions with 40,000 volunteers. At the same time, I want to say, "Vector" plans to conduct a clinical study among 150 people over 60 years old.'

    0 min read
    Availability: 
    Russia and other countries
    Generic: 
    EpiVakKorona
    Drug Class: 
    Peptide Subunit Vaccine
    Condition: 
    Last Reviewed: 
    Thursday, June 23, 2022 - 05:10
    Brand: 
    EpiVacCorona
    Status: 
    Manufacturer Country ID: