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VTP-500 MERS Vaccine

VTP-500 MERS Vaccine Clinical Trials, Dosage, Indication, Side Effects

Barinthus Biotherapeutics plc VTP-500 (ChAdOx1) vaccine candidate prevents the Middle East Respiratory Syndrome Coronavirus (MERS) Coronaviruses (CoV). The ChAdOx1 MERS vaccine candidate contains the replication-deficient simian adenovirus vector ChAdOx1, containing the MERS Spike protein antigen. VTP-500 MERS vaccine utilizes the ChAdOx1 virus platform to encode MERS coronavirus spike protein to induce T cells and antibodies that block virus-host cell receptor binding and fusion or neutralize virus infection.

The patented Vaccitech adenovirus vectors are known as chimpanzee adenovirus Oxford 1 and 2 (ChAdOx1 and ChAdOx2) and are in the group E simian adenovirus family, similar to the widely-studied chimpanzee adenovirus 63. These viruses have been engineered to be replication-deficient and manufactured in well-established HEK293 cell lines containing the adenoviral E1 gene. Vaccitech licensed the needed patents from Oxford University to advance its programs. The ChAdOx1 vector patent was granted in the US and the EU, and the MVA-NP+M1 patent was granted in the EU and is pending in the US. 

The University of Oxford’s Jenner Institute, in collaboration with The King Abdullah International Medical Research Centre (KAIMRC), announced on December 20, 2019, that it has started a Phase I clinical trial in the Kingdom of Saudi Arabia (KSA) for a vaccine against the MERS-CoV. VTP-500 has completed Phase I clinical trials in Britain and Saudi Arabia, and the University of Oxford is now extending the Phase Ib trial in the UK to assess vaccination of older adults.

On December 21, 2023, Barinthus Bio announced a project with the Coalition for Epidemic Preparedness Innovations (CEPI) and the University of Oxford, aiming to fast-track the development of a vaccine candidate known as VTP-500 to prevent MERS. The project will see CEPI, Barinthus Bio, and the University of Oxford take the MERS vaccine candidate from early development through Phase II clinical trials and, if the Phase II clinical trials are successful, develop an investigational ready reserve of 100,000 vaccines. Barinthus Bio will receive $34.8m in addition to previous funds that were committed to the University of Oxford and the CEPI will invest up to $47m to develop and stockpile the ready reserve of the MERS vaccine candidate. The development partners are committed to enabling equitable access to VTP-500 in line with CEPI’s Equitable Access Policy. Due to VTP-500’s potential to significantly address MERS outbreaks, the European Medicines Agency (EMA) confirmed support for the program through the PRIME designation. 

Oxford, England-based Barinthus Biotherapeutics plc (Vaccitech) (NASDAQ: BRNS) is an immunotherapy and vaccine company. The Company’s proprietary platform comprises proprietary modified simian adenoviral vectors, known as ChAdOx1 and ChAdOx2, and the well-validated Modified Vaccinia Ankara, or MVA, boost vector, both with demonstrable tolerability profiles and without the ability to replicate in humans. 

VTP-500 MERS Vaccine Indication

VTP-500 (ChAdOx1) vaccine candidate is designed to protect people against MERS-CoV.

VTP-500 MERS Vaccine News

December 21, 2023 - “Coronaviruses are one of the most urgent infectious disease threats the world faces, so it’s vital that we get on with developing medical defenses against this particularly deadly one – MERS,” said Dr. Richard Hatchett, CEPI’s Chief Executive Officer. “With this project, we will both advance scientific understanding of the coronavirus family as a whole and, at the same time, bolster humanity’s ability to respond to an ever-present epidemic threat.”

September 18, 2023 - A vaccine to protect people against MERS was launched in September 2023. This is the third Phase I clinical trial of the ChAdOx1 MERS vaccine.

August 12, 2021 - Vaccitech plc provided an overview of the Company’s recent corporate developments. 

April 29, 2021 - Vaccitech plc announced the pricing of its initial public offering in the United States for total gross proceeds of $110.5 million.

March 22, 2021 - Vaccitech Ltd. announces Joseph Scheeren, PharmD, as an independent director to its Board of Directors.

August 21, 2020 - CEPI, Oxford University, and Janssen have entered into a collaboration worth up to $19M to progress the vaccine through Phase 2 studies and establish a human vaccine stockpile with the University. 

June 10, 2020 - RESEARCH ARTICLE: A single dose of ChAdOx1 MERS provides protective immunity in rhesus macaques.

April 17, 2020 - NIH press release: Investigational chimp adenovirus MERS-CoV vaccine protects monkeys. Vaccine neutralizes multiple MERS-CoV strains.

December 20, 2019 - Vaccitech’s partner, the University of Oxford’s Jenner Institute, in collaboration with The King Abdullah International Medical Research Centre (KAIMRC), announced that it had started a Phase I clinical trial in the Kingdom of Saudi Arabia (KSA) for a vaccine against the Middle East Respiratory Syndrome Coronavirus (MERS-CoV). Vaccitech retains commercial rights to this vaccine. The trial will be the first Phase I clinical trial ever conducted in the KSA and will provide valuable clinical data. The trial is a collaboration between the Jenner Institute and the King Abdullah International Medical Research Center (KAIMRC), funded by the Department of Health and Social Care.

November 8, 2019 - Study: Humoral Immunogenicity and Efficacy of a Single Dose of ChAdOx1 MERS Vaccine Candidate in Dromedary Camels.The vaccination reduced virus shedding and nasal discharge (p = 0.0059 and p = 0.0274). The vaccine enhanced antibody responses in seropositive camels; these camels had a higher average age than seronegative. Older seronegative camels responded more strongly to vaccination than younger animals, and neutralizing antibodies were detected in nasal swabs.

VTP-500 Clinical Trials

Clinical Trial NCT04170829A Clinical Trial to Determine the Safety and Immunogenicity of Healthy Candidate MERS-CoV Vaccine. This research was funded by the Department of Health and Social Care (project number 16/107/01) as part of the UK Vaccine Network (UKVN), a UK Aid program to develop vaccines for diseases with epidemic potential in low and middle-income countries.

Findings: Between Dec 17, 2019, and June 1, 2020, 24 participants were enrolled (six to the low-dose, nine to the intermediate-dose, and nine to the high-dose group) and received a dose; 23 were available for follow-up at six months. The one dose of ChAdOx1 MERS vaccine was well tolerated with no serious adverse event reported during the six months of follow-up. Most adverse events were mild (67, 74%) and moderate (17, 19%). Six (7%) severe adverse events were reported by two participants in the intermediate-dose group (two feverish, two headache, one joint pain, and one muscle pain). Pain at the injection site was the most common local and overall adverse event, reported by 15 (63%) of the 24 participants. The most common systemic adverse event was headache, reported by 14 (58%), followed by muscle pain reported by 13 (54%). The vaccine-induced antibody and T cell immune responses in all volunteers; antibodies peaked at day 28, and T cell responses peaked at day 14 and continued until the end of follow-up at six months.

Clinical Trial NCT03399578: Suspended (The SARS-CoV-2 pandemic delayed recruitment but also provided an opportunity to apply findings from the rapid development of a ChAdOx1-vectored vaccine against SARS-CoV-2 to the further development of the MERS vaccine).

Findings: Between March 14 and Aug 15, 2018, 24 participants were enrolled: six were assigned to the low-dose group, nine to the intermediate-dose group, and nine to the high-dose group. All participants were available for follow-up at six months, but five (one in the low-dose group, one in the intermediate-dose group, and three in the high-dose group) were lost to follow-up at 12 months. A single dose of ChAdOx1 MERS was safe at doses up to 5 × 1010 viral particles with no vaccine-related serious adverse events reported by 12 months. One serious adverse event reported was deemed unrelated to ChAdOx1 MERS. 92 (74% [95% CI 66-81]) of 124 solicited adverse events were mild, 31 (25% [18-33]) were moderate, and all were self-limiting. Unsolicited adverse events in the 28 days following vaccination considered possibly, probably, or related to ChAdOx1 MERS were predominantly mild and resolved within the follow-up period of 12 months. The proportion of moderate and severe adverse events was significantly higher in the high-dose group than in the intermediate-dose group (relative risk 5·83 [95% CI 2·11-17·42], p<0·0001). Laboratory adverse events considered at least possibly related to the study intervention were self-limiting and predominantly mild in severity. A significant increase from baseline in T-cell (p<0·003) and IgG (p<0·0001) responses to the MERS-CoV spike antigen was observed at all doses. Neutralizing antibodies against live MERS-CoV was observed in four (44% [95% CI 19-73]) of nine participants in the high-dose group 28 days after vaccination, and 19 (79% [58-93]) of 24 participants had antibodies capable of neutralization in a pseudotyped virus neutralization assay.

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Availability: 
TBD
Generic: 
VTP-500
Drug Class: 
Vaccine
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Friday, May 10, 2024 - 05:45
Abbreviation: 
ChAdOx1 MERS vaccine
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FDA First In Class: 
Yes

VRC5283 Zika Virus Vaccine

VRC5283 Zika Virus Vaccine

VRC5283 is a Zika Virus DNA Vaccine candidate composed of a single closed-circular DNA plasmid that encodes with wild-type precursor transmembrane M and envelope proteins from the H/PF/2013 strain of ZIKV.  The vaccine was developed by the Vaccine Research Center, NIAID. VRC5283 is a new vaccine candidate that instructs the body to make a small amount of Zika virus protein. The body may use this to build an immune response.

An overview of the continuing development of vaccines and monoclonal antibodies against the Zika virus was published on May 24, 2024.

VRC5283 Vaccine Dosage

The vaccine is supplied in single-dose vials at a concentration of 4 mg/mL. ZIKV DNA vaccine dose will be 4 mg administered as an intramuscular (IM) injection in the deltoid muscle.

VRC5283 Vaccine News

December 4, 2017 - Gene-based Zika vaccine is safe and immunogenic in healthy adults

VRC5283 Clinical Trials

VRC5283 has completed two clinical trials.

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Generic: 
VRC5283
Drug Class: 
DNA plasmid
Condition: 
Last Reviewed: 
Thursday, June 20, 2024 - 05:50
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EXD-12 Herpes Simplex Vaccine

EXD-12 Herpes Simplex Vaccine Description 2022

EXD-12 is a live attenuated herpes simplex vaccine candidate. EXD-12 is going to be tested as a prophylactic and therapeutic vaccine candidate in the guinea pig model. EXD-12 is currently in preclinical testing for safety and efficacy as both a prophylactic and therapeutic vaccine for both Herpes Simplex Virus-1, HSV-1, and Herpes Simplex Virus-2, HSV-2.

For 30 years, vaccines against herpes viruses have failed to achieve U.S. FDA approval. Research groups have tried subunit vaccines repeatedly and failed. There is no cure for herpes. However, some medicines can prevent or shorten outbreaks, and preventive vaccines are in development.

Excell Biotech is setting out to clinically test a Herpes vaccine, which may also be a possible therapeutic intervention in humans. 

EXD-12 Indication

EXD-12 is currently in preclinical testing for safety and efficacy as both a prophylactic and therapeutic vaccine. Data indicates that glycoprotein D acts as a decoy, so the immune system cannot form an effective antibody response to other antigens. Without glycoprotein D, Herpes is visible to the immune system and is also unable to spread between cells.

The human population can either be infected with HSV1 (predominantly oral) or HSV2 (mostly genital). Most people think of it just as an annoyance, but there are many diseases associated with Herpes. Oral herpes is usually caused by HSV-1 and can result in cold sores or fever blisters on or around the mouth. However, most people do not have any symptoms. Most people with oral herpes were infected during childhood or young adulthood from non-sexual contact with saliva.

Genital herpes is common in the United States. More than one out of every six people aged 14 to 49 years have genital herpes. You can get genital herpes by having vaginal, anal, or oral sex with someone who has the disease. HSV-2 infection is more common among women than among men; the percentages of those infected during 2015-2016 were 15.9% versus 8.2% respectively, among 14 to 49-year-olds. This is possible because the genital infection is more easily transmitted from men to women than from women to men during penile-vaginal sex. Most people who have genital herpes have no symptoms or have very mild symptoms. You may not notice mild symptoms, or you may mistake them for another skin condition, such as a pimple or ingrown hair. Because of this, most people who have herpes do not know it.

Neonatal herpes is one of the most serious complications of genital herpes. Healthcare providers should ask all pregnant women if they have a history of genital herpes. Herpes infection can be passed from mother to child during pregnancy or childbirth, or babies may be infected shortly after birth, resulting in a potentially fatal neonatal herpes infection. Infants born to women who acquire genital herpes close to the delivery time and are shedding the virus at delivery are at a much higher risk of developing neonatal herpes than women with recurrent genital herpes.

EXD-12 News 2018 - 2022

June 15, 2022 - The Excell Team statedWe are about to start a study with the NIH to test our vaccine for pathogenesis and prophylactic capability in the animal model. Once that is complete, and if successful, we will be moving forward with a prophylactic study.

November 29, 2019: The company indicates it hopes to have its preclinical animal data completed by the end of 2019 and move into the clinic in early 2020.

September 14, 2018: Excell files a new provisional patent application with the United States Patent and Trademark office for their EXD-12 HSV vaccine candidate. New data indicates that glycoprotein D acts as a decoy, so the immune system cannot form an effective antibody response to other antigens. Without glycoprotein D, Herpes is visible to the immune system and can also be spread between cells.

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Generic: 
EXD-12
Drug Class: 
Vaccine Candidate
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Last Reviewed: 
Wednesday, August 24, 2022 - 05:45
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VBI-2601 Hepatitis B Vaccine

VBI-2601 (BRII-179) Vaccine Clinical Trials, Dosage, News, Side Effects, Usage

VBI Vaccines Inc. VBI-2601 (BRII-179) is a novel recombinant, protein-based immunotherapeutic hepatitis B vaccine candidate that targets B- and T-cell immunity through several key mechanisms of action, including neutralizing circulation of the hepatitis B virus (HVB) and blocking hepatocytes' infection Pre-S1 immunity, and enabling immune-mediated clearance of HBV-infected hepatocytes. VBI-2601 is uniquely formulated to target B-cell and T-cell immunity through multiple action mechanisms, including neutralizing the circulating hepatitis B virus, blocking hepatitis B infection of hepatocytes mediated through Pre-S1, and enabling immune-mediated clearance of HBV-infected hepatocytes. Many investigational agents work inside the infected liver cells downstream of transcription; BRII-179 is designed to impact the key extracellular steps in the HBV lifecycle to sustain immunologic control over the infection. VBI-2601 is being developed and led by Brii Bio in partnership with VBI Vaccines for patients with chronic HBV infection.

On February 15, 2023, the Company announced interim data from the Phase 2 study evaluating the combination of VBI-2601 (BRII-179) and BRII-835 (VIR-2218) in chronically infected HBV patients. The data, which will be featured in an oral presentation on February 18, 2023, demonstrated that the combination therapy was generally well-tolerated, restored strong anti-HBsAg antibody responses, and led to improved HBsAg-specific T-cell responses when compared to BRII-835 alone. Notably, in two participants who received the combination therapy, maximum reductions in HBsAg to an undetectable level or the lower limit of quantification (LLOQ) were achieved by Week 40, associated with robust HBV-specific antibody and T-cell responses. Based on the results of this study (ACTRN12619001210167), Brii Biosciences plans to conduct additional combination studies within the Asia-Pacific Economic Cooperation and the more significant China areas.

In July 2023, VBI and Brii Bio announced an expansion of their HBV partnership to include an exclusive global license to develop and commercialize BRII-179 (VBI-2601) and an exclusive license to develop and commercialize PreHevbri®, VBI's prophylactic 3-antigen adult HBV vaccine, in the Asia Pacific region, excluding Japan.

On September 6, 2023, the Company announced topline cohort-level unblinded Week 24 and Week 36 data from interim analysis of a randomized, placebo-controlled, and double-blinded Phase 2 study of BRII-179, a first-in-class Pre-S1/Pre-S2/S therapeutic vaccine, in combination treatment with pegylated interferon-alpha (PEG-IFNα) in patients with chronic hepatitis B (CHB) compared with PEG-IFNα only treatment.

On February 13, 2024, Brii Biosciences Limited announced that it has entered into agreements with VBI Vaccines, Inc., ensuring expansion and control of future clinical and commercial supplies of BRII-179. Brii Bio had commercial rights to BRII-179 (VBI-2601) in the licensed territories of China, Hong Kong, Macau, and Taiwan. Brii Bio will also take control of VBI's Rehovot-based manufacturing facilities for BRII-179 and PreHevbrio/PreHevbri. With operations in the People's Republic of China and the United States, Brii Bio is poised to serve as a bridge to carry transformative medicines to patients, help create significant growth for our partners, and establish an innovation engine to help improve the public health and wellbeing of patients around the world.

VBI Vaccines Inc. is a commercial-stage biopharmaceutical company developing the next generation of vaccines to address unmet infectious disease and immuno-oncology needs. VBI (Nasdaq: VBIV).

VBI-2601 (BRII-179) Vaccine Indication

BRII-179 (VBI-2601) is a novel recombinant, protein-based immunotherapeutic candidate developed and led by Brii Bio in partnership with VBI Vaccines for patients with chronic HBV infection. VBI-2601 is indicated as the functional cure for treating chronic hepatitis B infection. Hepatitis B infection is the most prevalent global infection, with 250 million infected worldwide, according to the U.S. CDC. Global HBV infection is rampant, and there is also a high unmet need for effective therapies, as current treatments generate a functional cure in less than 10 percent of those treated. Achieving a functional cure, therefore, is a global health priority.

VBI-2601 (BRII-179) Vaccine Dosage

A two-part dose-escalation study assessing a low dose and a high dose of VBI-2601 (BRII-179), with and without an undisclosed adjuvant, has enrolled 46 patients. BRII-179 (VBI-2601) was given by intramuscular injection. On June 23, 2021, 20 μg and 40 μg doses of BRII-179 (VBI-2601) with and without low dose IFN-α administered through intramuscular injection were well-tolerated with no significant adverse events identified.

VBI-2601 (BRII-179) Vaccine Side Effects

A phase 3 study found vaccine discontinuation due to adverse events was uncommon, and serious AEs were infrequent, reported in 42 participants (2%) and 3 participants (0.4%) in the 3A-HBV and 1A-HBV groups, respectively.

VBI-2601 (BRII-179) Vaccine News

February 13, 2024—Dr. Zhi Hong, Ph.D., Chairman and Chief Executive Officer of Brii Bio, stated, "As Brii transitions to late-stage development of HBV programs, a global manufacturing strategy becomes critically important. We look forward to working with the biologics manufacturing experts at the Rehovot site and timely integrating our R&D and manufacturing capabilities."

September 6, 2023 - "We are excited by the data from this proof-of-concept study, which are consistent with our previous proof-of-mechanism studies that BRII-179 induces functional immune responses complementing other curative treatment modalities such as PEG-IFNα," said David Margolis, MD, Chief Medical Officer of Brii Bio.

February 15, 2023 - VBI-2601 (BRII-179) and BRII-835 combination were generally well-tolerated, with no new safety signals observed. The Initial study data suggest that VBI-2601 (BRII-179) and BRII-835 combination induced meaningfully more potent anti-hepatitis B surface antigen (HBsAg)-specific T-cell and antibody responses compared to BRII-835 alone. Data will be featured in an oral presentation by Dr. Man Fung Yuen, M.D., Ph.D., D.Sc., on February 18, 2023.

January 5, 2022 - VBI Vaccines Inc. announced that the first patient had been dosed in a second Phase 2a/2b clinical study evaluating VBI-2601 (BRII-179). This newly announced Phase 2 study will assess VBI-2601 as an add-on therapy to the standard-of-care, nucleos(t)ide reverse transcriptase inhibitor and pegylated interferon (PEG-IFN-α) therapy, which currently has a functional cure rate of approximately 9%. Data from these two Phase 2 studies could become available in the second half of 2022 and the first half of 2023, respectively.

November 3, 2021 - The U.S. CDC's ACIP unanimously passed a universal HBV vaccination recommendation for all adults aged 19-59 and adults aged 60+ with risk factors for infection. The U.S. PDUFA target action date is November 30, 2021.

August 2, 2021 - VBI Vaccine provided a corporate update.

June 23, 2021 - Brii Biosciences and VBI Vaccines Inc. announced final results from a Phase 1b/2a study on BRII-179 (VBI-2601), a novel recombinant, protein-based immunotherapeutic candidate, in patients with chronic hepatitis B virus (HBV) infection. Data from the study, which evaluated the safety, antiviral activity, and immunogenicity of BRII-179 (VBI-2601) alone or admixed with interferon-alpha as a co-adjuvant, demonstrated that the investigational immunotherapeutic induced both B cell (antibody) and T cell responses and was well-tolerated with no safety signals observed, in non-cirrhotic chronic hepatitis B patients under nucleos(t)ide analog therapy. Furthermore, BRII-179 (VBI-2601) induced and/or boosted S-, Pre-S1-, and/or Pre-S2-specific IFN-gamma producing T cells in 77% of patients across all treatment cohorts, compared to no detectable response in patients in control, NUC-only arm. Additionally, BRII-179 induced hepatitis B antibody responses in 44.2% of patients in the BRII-179 treatment arms.

June 9, 2021 - Brii Biosciences announced that it would present the complete dataset from its Phase 1b/2a study evaluating BRII-179 (VBI-2601) as a treatment for chronic hepatitis B virus (HBV) infection as a late-breaker ePoster at the European Association for the Study of the Liver's (EASL) International Liver Congress 2021, which is taking place virtually from June 23-26, 2021.

May 10, 2021 - VBI Vaccines Inc. reported financial results for the first quarter ending March 31, 2021, and provided a corporate update. Additional data from Phase 1b/2a study in chronic HBV patients demonstrated robust HBV-specific T cell and antibody responses across all study arms.

April 21, 2021 - Vir Biotechnology, Inc. (Nasdaq: VIR), VBI Vaccines Inc., and Brii Biosciences announced that the first patient had been dosed in Phase 2 clinical study evaluating BRII-835 (VIR-2218), an investigational small interfering ribonucleic acid-targeting hepatitis B virus (HBV), in combination with BRII-179 (VBI-2601), an investigational HBV immunotherapeutic, for the treatment of chronic HBV infection. This is the first clinical trial in the field to evaluate the combination of these two HBV mechanisms of action.

March 2, 2021 - VBI Vaccines Inc. announced financial results for the fourth quarter and twelve months ended December 31, 2020. The Company also provided a corporate update and its outlook for 2021. Partner Brii Biosciences is expected to initiate a Phase 2 combination study to assess VBI-2601 (BRII-179) and BRII-835 (VIR-2218), a novel RNAi therapeutic potential functional cure in chronically infected patients.

December 17, 2020 - Interim data from a Phase 1b/2a trial designed to assess the safety, tolerability, and antiviral activity of BRII-179 (VBI-2601), a novel recombinant, protein-based immuno-therapeutic, demonstrated the induction of both antibody and T cell responses in chronically infected HBV patients. The Company announced that recruitment was completed for a Phase 2 clinical trial for BRII-835 (VIR-2218), a novel, investigational RNA interference (RNAi) therapeutic designed to inhibit the expression of all HBV proteins, including hepatitis B surface antigen (HBsAg). Interim results are expected in the second quarter of 2021. During the first quarter of 2021, the Company is also preparing to launch a Phase 2 clinical trial examining the safety and efficacy of BRII-179 and BRII-835 in combination with patients on the stable nucleus (t)ide therapies.

November 18, 2020 - VBI Vaccines Inc. announced positive interim clinical results from the ongoing Phase 1b/2a study of VBI-2601 (BRII-179), a novel recombinant, protein-based immunotherapeutic candidate for the treatment of chronic hepatitis B virus infection, in development in collaboration with Brii Biosciences.

November 14, 2019 - VBI Vaccines Inc. and Brii Biosciences ("Brii Bio") announced the first patient dosed in Phase 1b/2a proof-of-concept study of BRII-179 (VBI-2601), a novel recombinant, a protein-based immuno-therapeutic candidate in development for the treatment of chronic hepatitis B virus infection.

VBI-2601 (BRII-179) Vaccine Clinical Trial

Brii Biosciences is the sponsor of this newly announced Phase 2a/2b study and, with the support of VBI, has led the design and implementation of this study and the ongoing Phase 2 combination study. The Phase 2a/2b trial of VBI-2601 (BRII-179) is a double-blind, randomized, placebo-controlled, parallel-group study to evaluate the clinical effect of adding VBI-2601 (BRII-179) to existing PEG-IFN-α and Nrtl standard-of-care therapy in non-cirrhotic chronic HBV patients. Patients participating in the study have had partial responses to ongoing PEG-IFN-α and NrtI treatment.

The phase 2, multicenter, randomized, open-label study is designed to evaluate the safety and efficacy of BRII-835 (VIR-2218) compared to the combination of BRII-835 (VIR-2218) and BRII-179 (VBI-2601) with and without interferon-alpha as a co-adjuvant. Both agents have demonstrated proof of mechanism in HBV patients (NCT04507269 BRII-835 China study and ACTRN12619001210167 BRII-179 APEC study). Brii Bio has led the design and implementation of this functional cure proof-of-concept study with the support of VIR and VBI and is the sponsor of the Phase 2 study (NCT04749368). It will be conducted at sites in Australia, China, Taiwan, Hong Kong, the Special Administrative Region of China, South Korea, New Zealand, Singapore, and Thailand.

Clinical Trial ACTRN12619001210167: A Study to Evaluate Safety, Tolerability, and Antiviral Activity of BRII-179 (VBI-2601) among Subjects with Chronic Hepatitis B. A Phase 1b/2a clinical study of BRII-179 (VBI-2601) is a randomized, controlled study designed to assess the safety, tolerability, and antiviral activity of BRII-179 (VBI-2601) in patients with chronic HBV infection.

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Availability: 
TBD
Generic: 
VBI-2601 (BRII-179)
Drug Class: 
Recombinant, protein-based immunotherapeutic vaccine
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Last Reviewed: 
Saturday, March 23, 2024 - 06:30
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Manufacturer Country ID: 

ChiroRab Rabies Vaccine

ChiroRab® Rabies Vaccine

Chirorab® (Rabipur) is an inactivated rabies virus of the strain Flury LEP, a purified chick embryo cell (PCEC) vaccine. Chirorab is an injectable vaccine given to people of any age at higher risk of contracting with rabies-like veterinarians. It is also given to people if it could have rabies after an animal bite. If the vaccine is given immediately and appropriately, it is 100% effective.

Chiron Behring Vaccines are manufactured at its WHO pre-qualified facility in Ankleshwar, Gujarat. Bharat Biotech acquired the company in 2019. Bharat Biotech is a pioneering biotechnology company based in Pune, India, known for its world-class R&D and manufacturing capabilities.

ChiroRab Rabies Vaccine Indication

Chirorab is a vaccine that is used for active pre-post-exposure immunization against Rabies. Post-exposure anti-rabies vaccination should always include the administration of both Immunoglobulin and vaccine, except for persons who have previously received complete vaccination regimens. Therefore, it is essential to complete the vaccine course to prevent this fatal disease. Chirorab may be individuals previously immunized with any human diploid cell rabies vaccine. In addition, ChiroRab can be used in individuals of all ages.

ChiroRab Rabies Vaccine Dosage

The immunogenicity, efficacy, and safety of Chirorab have been assessed in several clinical trials in pre-and post-exposure regimens, using both intramuscular and intradermal routes of administration.

ChiroRab Rabies Vaccine Adverse Reactions

Anaphylactic reactions, including anaphylactic shock that are rare but clinically severe and potentially lethal, systemic allergic reactions, can occur following vaccination. In addition, mild allergic reactions may occur after vaccination, including rashes (widespread) and urticaria (common); these reactions are usually mild and typically resolve within a few days. However, sporadic cases with symptoms of Encephalitis and Guillain-Barré Syndrome have been reported. In clinical trials, the most commonly reported solicited adverse reactions were injection site pain (30-85%) or injection site induration (15-35%). However, most injection site reactions were not severe and resolved within 24 to 48 hours.

ChiroRab Rabies Vaccine News

January 23, 2023 - Bharat Biotech announced on Twitter: "We have issued a voluntary product recall of a specific batch of Chirorab with batch number 4188. This action was initiated due to the theft of Chirorab from the shipping services provider in Karnataka," the company said in a statement. It added that the company had tested batch No. 4188 and released it, but part of the shipment was stolen, for which cold chain storage conditions are unknown. The action to recall the entire batch has been initiated. "We are undertaking this voluntary action by the Principle of Abundant Precaution.

May 20, 2022 - The U.S. CDC has published a warning that rabies could be re-imported into the U.S. after a rescue puppy tests positive for the virus.

December 29, 2020 - Indian Scientists discover the rabies virus's effect on the host brain, a step closer to a cure. After entering the body, the virus remains dormant for 20 to even 90 days without showing any clinical symptoms. When symptoms emerge, little time is available to offer effective treatment. Death occurs within two to seven days. Fatality is thus almost 100 percent. 

November 13, 2019 - Chiron Behring Vaccines, part of Bharat Biotech International Ltd., announced the relaunch of Rabipur as Chirorab. "In our ongoing commitment to address the supply shortages of rabies vaccine, we are making additional investments to increase production capacities to over 15 million doses annually," said Dr. Krishna Ella, CMD of Bharat Biotech.

ChiroRab Rabies Vaccine Clinical Trials

Clinical Trial NCT02545517: A Clinical Study to Evaluate Immune Responses to Rabies Vaccine in Adults Who Received Different Primary Rabies Vaccination Regimens.

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Availability: 
India
Generic: 
rabies vaccine
Drug Class: 
Vaccine
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Last Reviewed: 
Saturday, February 10, 2024 - 07:40
Brand: 
Chirorab
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Manufacturer Country ID: 
Halal: 
Yes
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zvovJ4nt

MV-LASV Lassa Fever Vaccine

MV-LASV Lassa Fever Vaccine Candidate Clinical Trials, Dosage, News, Side Effects, Usage

MV-LASV is a recombinant, live-attenuated, viral vectored Lass fever (LF) vaccine candidate based on the backbone of the measles Schwarz virus strain for prophylaxis of Lassa infection. On October 29, 2019, Themis Bioscience and the Coalition for Epidemic Preparedness Innovations announced the first administration to healthy volunteers in a Phase 1 clinical trial with Themis’ vaccine candidate against Lassa fever. 

On March 16, 2023, The Lancet published Immunogenicity, safety, and tolerability of a recombinant measles-vectored Lassa fever vaccine: a randomized, placebo-controlled, first-in-human trial. Interpretation: MV-LASV showed an acceptable safety and tolerability profile, and immunogenicity seemed to be unaffected by pre-existing immunity against the vector. MV-LASV is, therefore, a promising candidate for further development. The Coalition for Epidemic Preparedness Innovations funded this phase 1 study.

According to the World Health Organization, LF vaccines should be cost-effective, affordable in endemic areas, and stable for a reasonable time without extensive cold chain facilities.

In June 2020, Merck acquired Themis, a privately held company focused on vaccines and immune-modulation therapies for infectious diseases and cancer.

MV-LASV Indication

MV-LASV vaccine candidate is indicated for at-risk populations during outbreaks of Lassa Fever, an emerging infectious disease. Lassa fever is an acute viral hemorrhagic disease caused by the Lassa virus (LASV). It is endemic in West Africa and infects about 300,000 people yearly, leading to approximately 5000 deaths annually. Therefore, the World Health Organization has listed the development of the LASV vaccine as a priority since 2018. 

MV-LASV Dosage

MV-LASV is administered at two different dose levels intramuscularly. Injection. The aim is to investigate the safety, tolerability, and immunogenicity of MV-LASV after administering two different dose levels of MV-LASV. 

MV-LASV Clinical Trial

Clinical Trial NCT04055454: A Trial to Evaluate the Optimal Dose of MV-LASV—The trial is complete and registered with the European Union Drug Regulating Authorities Clinical Trials Database, 2018-003647-40.

Findings - Between September 26, 2019, and January 20, 2020, 60 participants were enrolled and assigned to receive a placebo (n=12) or MV-LASV (n=48). All 60 participants received at least one study treatment. Most adverse events occurred during the treatment phase. Frequencies of total solicited or unsolicited adverse events were similar between treatment groups, with 96% of participants in the low-dose group, 100% of those in the high-dose group, and 92% of those in the placebo group having any solicited adverse event (p=0·6751) and 76% of those in the low-dose group, 70% of those in the high-dose group, and 100% of those in the placebo group having any unsolicited adverse event (p=0·1047). The only significant difference related to local solicited adverse events, with higher frequencies observed in groups receiving MV-LASV (24 [96%] of 25 participants in the low-dose group; all 23 [100%] participants in the high-dose group) than in the placebo group (6 [50%] of 12 participants; p=0·0001, Fisher-Freeman-Halton test). Adverse events were mainly of mild or moderate severity, and no serious adverse events were observed. MV-LASV also induced substantial concentrations of LASV-specific IgG (geometric mean titre 62·9 EU/ml in the low-dose group and 145·9 EU/ml in the high-dose group on day 42).

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TetraVax-DV (V180) Dengue Vaccine

TetraVax-DV (V180) Dengue Vaccine Clinical Trials, Dosage, News, Side Effects, Usage

Merck & Co., Instituto Butantan, and Medigen Vaccine Biologics (MVB), co-developed TetraVax-DV, V180, Butantan-DV, and TV003) adjuvanted, tetravalent subunit dengue vaccine candidate comprised truncated forms of envelope proteins (DEN-80E), derived from strains of all four dengue virus serotypes (DEN-1 strain 258848, DEN-2 strain PR159 S1, DEN-3 strain CH53489, and DEN-4 strain H241). The DEN-80E subunits are expressed from plasmids in the Drosophila S2 cell expression system and are formulated with either ISCOMATRIX (saponin, cholesterol, and phospholipid adjuvant; CSL) or Alhydrogel (aluminum hydroxide gel adjuvant; Brenntag Nordic).

In 2024, according to a phase 3 clinical study conducted in Brazil, the V180 vaccine candidate was found to be 79.6% effective in preventing dengue. During this period, no serious dengue cases were reported in the participants. The positive result is the result of more than ten years of work with international partners. In the phase 2 clinical trial, the results were published in an article in The Lancet Infectious Diseases. According to the clinical study report, no vaccine-related SAEs were observed in 54 subjects aged 20-70. The immunogenicity data demonstrates that the vaccinated group produced higher neutralizing antibody titers (GMTs of PRNT50, and had a higher seropositivity rate against types of Dengue virus than the controlled group. Moreover, the vaccinated group remained expressing neutralizing responses on day 180 and day 365 after vaccination, this result reveals that MVC's dengue vaccine shows immunogenicity not only within 20-50-year-old subjects but also in the elder group aged 51-70 years old.

Development of the tetravalent dengue vaccine began at Butantan Institute in 2010 with FAPESP's support (Grant number: 08/50029-7), using a formulation created by researchers affiliated with the US National Institutes of Health (NIH). Clinical trials in Brazil began in 2013, with the support of the Butantan Foundation and BNDES, Brazil's national development bank, under the aegis of the project "Development of a tetravalent dengue vaccine," led by Neuza Frazatti Gallina, winner of the 2023 Péter Murányi Prize.

On December 16, 2022, Merck announced, 'We are highly encouraged by the tremendous progress scientists and clinicians at the Instituto Butantan have made in developing their single-dose dengue vaccine candidate.' In February 2024, infectious disease specialist Esper Kallás informed Agência FAPESP, "In June (2024), we'll complete the five-year follow-up period. Once the data has been consolidated, we'll know how long the vaccine-induced protection will last."

Instituto Butantan, in São Paulo state, Brazil, is the largest producer of vaccines and serums in Latin America and the main producer of immunological products in Brazil. MVC is a biopharmaceutical company focusing on developing and mass-producing vaccines and biologics. It is located at No. 68, Shengyi 3rd Rd., Zhubei City, Hsinchu County 302, Taiwan (R.O.C.).

TetraVax-DV (V180) Vaccine Dosage

V180 is administered as an intramuscular injection. A single dose schedule was evaluated in the phase 3 study. The two-dose schedule could still be improved to reduce the risk of non-compliance. However, it is believed that V180 would achieve significant commercial potential as part of a heterologous prime-boost strategy.

TetraVax-DV (V180) Dengue Vaccine News

February 1, 2024 - The NEJM published an Original Article - Live, Attenuated, Tetravalent Butantan–Dengue Vaccine in Children and Adults.

April 8, 2023 - The phase II study for the dengue vaccine in Taiwan finished the bridging and proof-of-concept study assessed ethnic differences and evaluated the immunogenicity of the elderly population.

December 16, 2022 - Butantan confirmed its dengue vaccine is 79.6% effective in phase 3 study results.

April 13, 2022 - A new strain of dengue was detected in Brazil in a man from Aparecida de Goiânia by researchers from the Oswaldo Cruz Foundation and the Central Public Health Laboratory of Goiás. The serotype two genotype, also known as the cosmopolitan genotype, is the most widespread dengue virus lineage globally, but it had never been found in Brazil.

March 24, 2020 - The Lancet published a study: Safety and immunogenicity of the tetravalent, live-attenuated dengue vaccine Butantan-DV in adults in Brazil: a two-step, double-blind, randomized placebo-controlled phase 2 trial. Butantan-DV and TV003 were safe and induced robust, balanced neutralizing antibody responses against the four DENV serotypes. The efficacy evaluation of the Butantan-DV vaccine is ongoing.

February 15, 2018 - Global Drug Analysis: V180 - More Compact Dosing Schedule Could Make It a More Attractive Alternative to Dengvaxia.

V180 Dengue Vaccine Clinical Trials

ClinicalTrials NCT02406729: Over a 3-year enrollment period, 16,235 participants received either Butantan-DV (10,259 participants) or placebo (5976 participants). The overall 2-year vaccine efficacy was 79.6% (95% confidence interval [CI], 70.0 to 86.3) — 73.6% (95% CI, 57.6 to 83.7) among participants with no evidence of previous dengue exposure and 89.2% (95% CI, 77.6 to 95.6) among those with a history of exposure.

Clinical Trial NCT02450838: Evaluating the Safety, Tolerability, and Immunogenicity of a Tetravalent Dengue Vaccine (V180) in Healthy Adults Who Previously Received a Live-Attenuated Tetravalent Vaccine (TV003 or TV005).

Clinical Trial NCT01477580:  Study of a Dengue Vaccine (V180) in Healthy Adults (V180-001) (Completed, No results posted).

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IVX-121 Respiratory Syncytial Virus (RSV) Vaccine

IVX-121 RSV hMPV Vaccine May 2023

Icosavax, Inc. IVX-121 is a bivalent respiratory syncytial virus (RSV) and human metapneumovirus (hMPV) vaccine candidate that incorporates a stabilized prefusion F antigen licensed from NIAID/NIH (DS-CAV1). IVX-121 applies Vaccine-Like Particles (VLP) technology to the DS-CAV1. VLPs enable a high-density, multivalent display of antigens in a manner that closely resembles viruses, with a significant difference. RSV and hMPV VLPs employ the F protein responsible for viral cell entry. F proteins undergo conformational changes upon fusing to the cell membrane; utilizing prefusion F protein may lead to higher nAb titers. In addition, VLPs contain no genetic material, so they are non-infectious and can provide a safer alternative to live-attenuated or inactivated vaccines. This technology enables a high-density, multivalent display of antigens in a manner that closely resembles the structure of a virus.

A Phase 1/1b trial involving the RSV component of the combination vaccine, IVX-121, was initiated in September of 2021. The IVX-121 (RSV) component of IVX-A12 (RSV/hMPV) previously demonstrated positive immunogenicity and tolerability results in a Phase 1/1b study, and a subset of these Phase 1b older adult subjects continue to be followed. In December 2022, Icosavax reported positive durability data at six months, with twelve-month immunogenicity data expected in mid-2023. Pending results from the planned Phase 2 trial, Icosavax intends to conduct an IVX-A12 hMPV human challenge clinical trial, which Icosavax considers the most relevant proof-of-concept model for evaluating disease prevention for its bivalent vaccine candidate incorporating stabilized prefusion F proteins for each of RSV and hMPV. This hMPV human challenge model is currently in development and builds on an established precedent in the RSV field.

On February 21, 2023, the Company announced the U.S. Food and Drug Administration (FDA) had granted Fast Track designation for the IVX-A12 VLP vaccine candidate.

"The topline interim data from our Phase 1 trial show that IVX-A12 was generally well tolerated and elicited a robust response against RSV and hMPV in older adults, with no evidence of immune interference. This is an important result as IVX-A12 is the only vaccine candidate in clinical development targeting both RSV and hMPV in older adults, a vulnerable population with a heightened risk of severe disease," said Niranjan Kanesa-thasan, M.D., Chief Medical Officer of Icosavax, on May 22, 2023.

Seattle-based Icosavax's focus is developing high-impact vaccines against infectious diseases to improve human health.

IVX-121 Indication

IVX-121 is a vaccine candidate for RSV and hMPV, which are related Pneumoviridae. Both viruses are expected, with high re-infection rates.

IVX-121 Dosage

IVX-121 is administered as an intramuscular injection. In phase 1, subjects were administered a single dose of IVX-A12 at one of three combination dosage levels or placebo: 150 µg total VLP content (75 µg of IVX-121 (RSV) and 75 µg of IVX-241 (hMPV)), with or without MF59®; 225 µg total VLP content (75 µg of IVX-121 and 150 µg of IVX-241), with or without MF59; 300 µg total VLP content (75 µg of IVX-121 and 225 µg of IVX-241), without MF59.

IVX-121 News

May 22, 2023 - The Company announced positive topline interim results from its Phase 1 clinical trial of IVX-A12 against RSV and hMPV in older adults.

June 10, 2021 - Icosavax Appoints Thomas J. Russo, Chief Financial Officer. Mr. Russo brings over 25 years of diverse industry experience, including in finance and operations for public biotechnology companies, as a sell-side equity research analyst covering biotechnology, and in operations and vaccine manufacturing for a large pharma company.

April 7, 2021 - Icosavax Closes $100 Million Series B Financing to Advance Bivalent RSV/hMPV Vaccine Candidate Into Clinical Trials

May 13, 2020 - Icosavax's RSV vaccine, IVX-121, is expected to enter clinical trials in 2021. It uses the stabilized prefusion F antigen DC-Cav1, licensed from the National Institute of Allergy & Infectious Diseases at the National Institutes of Health. Preclinical studies suggest IVX-121 is ten times more effective than the DS-Cav1 antigen alone at neutralizing RSV.

October 3, 2019 - Icosavax announces $51 Million Dollars Raised For RSV Vaccine Development. Extensive preclinical studies conducted at IPD and Icosavax suggest that IVX-121 could increase the protective immunogenicity of RSV F compared to the DS-Cav1 antigen alone.

IVX-121 Clinical Trial

Phase 1 trial results, IVX-A12 induced robust immune responses against both RSV and hMPV at Day 28 in older adults across dosage levels and with and without adjuvant. There was no evidence of immune interference between RSV and hMPV VLPs when administered in combination. Across dosage groups, IVX-A12 induced geometric mean titers (GMTs) in RSV-A neutralizing antibody titers (nAbs) of up to approximately 16,100 IU/mL compared to approximately 2,600 IU/mL for placebo at Day 28. IVX-A12 induced GMTs in RSV-B nAbs of up to approximately 8,300 IU/mL compared to approximately 2,500 IU/mL for placebo at Day 28. There were higher Day 28 post-vaccination levels of RSV A and RSV B nAbs (IU/ml) observed in this IVX-A12 study than in the previous Phase 1 clinical study of IVX-121 (RSV) alone.

Across dosage groups, IVX-A12 induced GMTs in hMPV-A nAbs of up to approximately 3,300 assay units/mL compared to approximately 900 assay units/mL for placebo at Day 28. IVX-A12 induced GMTs in hMPV-B nAbs of up to approximately 23,900 assay units/mL compared to approximately 11,500 assay units/mL for placebo at Day 28. No standardized international units exist in the field for hMPV. High baseline nAbs to RSV-A and RSV-B were observed, likely reflecting an off-cycle RSV season following the COVID-19 pandemic. Geometric mean fold rise (GMFR) at Day 28 was up to 4-fold in RSV-A and 3-fold in RSV-B across all treatment groups. In a pre-specified sub-analysis of data from subjects with the lowest tertile baseline nAbs titers, the corresponding GMFRs for RSV-A and RSV-B were up to 11-fold and 7-fold, respectively. GMFR at Day 28 was up to 5-fold in hMPV-A and 4-fold in hMPV-B. In a pre-specified sub-analysis of data from subjects with the lowest tertile baseline nABs titers, the corresponding GMFRs for hMPV-A and hMPV-B were up to 9-fold and 8-fold, respectively.

In a Phase 1 clinical study conducted by NIAID/NIH, DS-Cav1 induced robust neutralizing antibody titers, higher than titers demonstrated in previous studies with RSV postfusion F vaccine candidates. In addition, extensivepreclinical studies suggest that the VLP display of DS-Cav1 in IVX-121 induces higher and more durable neutralizing antibody titers compared to the DS-Cav1 antigen alone, and the presentation of DS-Cav1 on the VLP confers improved stability.

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Generic: 
IVX-121
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VLP Vaccine
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Bacille Calmette-Guerin (BCG) Vaccine

Bacille Calmette-Guérin (BCG) Vaccine Clinical Trials, Dosage, Efficacy, Indications, Side Effects

In 1921, French scientists Albert Calmette and Camille Guérin developed the initial Mycobacterium bovis Bacillus Calmette-Guérin (BCG) vaccine. The BCG vaccine was designed to protect cattle from bovine tuberculosis and was administered to a newborn baby in Paris. BCG-induced whole-blood cytokine levels differ by age, vaccine formulation, and concentration. In addition, BCG-induced cytokine production correlated with CFU, suggesting that mycobacterial viability may contribute to BCG-induced immune responses. Mycobacterium tuberculosis (Mtb) is the etiological agent of tuberculosis (TB).

Since 1921, BCG vaccines have been administered approximately 4 billion times worldwide. BCG vaccines initially targeted against TB, tuberculosis meningitis, and non-specific protective effects against other respiratory tract infections and certain cancers. In naive adult populations, the BCG vaccine, administered as an intradermal injection, takes at least two years to achieve complete protection due to several off-target effects. A study published in September 2023 characterized the mechanisms of BCG revaccination-induced trained immunity (TI). Data highlights a balanced immune response comprising pro- and anti-inflammatory mediators, a feature of BCG revaccination-induced immunity. These immune responses have been used to prevent and treat various diseases, including bladder cancer, herpes, human papillomavirus, leprosy, and Buruli ulcers.

BCG immunization or MTB infection of the human body induces an increase in gene rearrangement and metabolism in intrinsic immune cells, such as macrophages, NK cells, and monocytes, leading to the increased secretion of cytokines, including TNF-α, IL-1β, and IL-6. During reinfection with other pathogens, such as HSV-1, these trained innate immune cells rapidly secrete TNF-α, IL-1β, IL-6, and other cytokines to eliminate invading pathogens.

A study reported in July 2024 found that the immune response to M. tuberculosis (Mtb) is associated with the activation of type 1 T helper (Th1) responses and the production of a range of cytokines, including tumor necrosis factor-alpha (TNF-α) and interferon-gamma (IFN-γ). Genetic defects, such as mutations in cytokine receptors like interleukin-12 (IL-12) or IFN-γ, enhance the cell differentiation, leading to increased susceptibility to progressive mycobacterial disease. In addition, the neutralization of TNF-α by monoclonal antibodies (such as those used in treating rheumatoid arthritis) can prevent LTBI reactivation. 

On January 19, 2021, Dr. Camille Locht, research director at Inserm's Institut Pasteur de Lille, stated, "The BCG can train the cells of the innate immune system to make them more fit and active to fight against other diseases." The U.S. National Institutes of Health (NIH) says the BCG vaccine is safe. The BCG vaccine is used in many countries (Mexico, the U.K., Canada) for emerging therapeutic off-target benefits, such as treating bladder cancer. As of February 2023, the biological interaction between M. tuberculosis (Mtb) and the human host is complex and only partially understood, according to the World Health Organization (WHO). The WHO 2022 Report says BCG vaccination should continue for all infants soon after birth, except for those living with HIV in high tuberculosis-prevalence settings. The WHO adopted requirements for the BCG vaccine in 1965, and these were updated in 1978 to reflect the increased knowledge of vaccinations and the change to freeze-dried preparations. These were modified in 1985 to amend requirements concerning the expiry date. In its thirteenth report, the WHO Expert Committee on Biological Standardization considered formulating international requirements for manufacturing and controlling the BCG vaccine. On September 30, 2022, the WHO published consolidated guidelines on TB, Module 3. The WHO recommends BCG vaccination at birth in countries where tuberculosis is endemic. In 2024, the U.K.'s NHS states that the BCG vaccine will be particularly beneficial in protecting babies and young children against more severe forms of TB.

On August 5, 2022, new research (MIS BAIR) led by the Murdoch Children's Research Institute in Australia and published in the peer-reviewed Science Advances journal showed how BCG vaccination produces 'trained immunity responses' lasting more than 14 months after administration. On August 15, 2022, research findings published by the Cell Reports Medicine journal suggested that the BCG platform protects against infectious diseases and that vaccine efficacy takes 1-2 years to manifest, but the protection may last decades. The Rockefeller Foundation announced on September 20, 2022, that it would commit US$15 million to the Global Fund to Fight AIDS, TB, and Malaria.

BCG Vaccine United States

Merck TICE® BCG vaccine is an attenuated, strain tice live antigen preparation of Mycobacterium bovis. The TICE strain was developed at the University of Illinois from a strain originating at the Pasteur Institute. Since 2012, Merck & Co. has been the supplier of the TICE BCG vaccine in the U.S. Merck confirmed it was experiencing a global shortage due to the growing demand for BCG vaccines. In October 2020, Merck announced plans to construct a manufacturing facility in Durham, North Carolina, to expand production of the TICE BCG vaccine.

The U.S. Centers for Disease Control and Prevention (CDC) states that the BCG vaccine is not generally recommended for use in the U.S. due to the minimal risk of infection with Mycobacterium tuberculosis. The CDC recommends BCG vaccination only for children who have a negative tuberculin skin test and are at ongoing risk of exposure to tuberculosis. BCG vaccination may be recommended for older children who have an increased risk of developing TB, such as children who have recently arrived from countries with high levels of TB, including those in Africa, the Indian subcontinent, parts of southeast Asia, parts of South and Central America, and parts of the Middle East, and children who have come into close contact with somebody infected with respiratory TB. Many foreign-born persons have been BCG-vaccinated. BCG is used in many countries with a high prevalence of TB to prevent childhood tuberculous meningitis.

BCG Vaccines 2025

As of 2025, various BCG vaccines are available globally, including TUBERVAC-rBCG, BCG vaccine AJV (A.J. Vaccines), VERITY-BCG™, France BCG vaccine (Pasteur 1173P2), Brazil strain (BCG oral Mearou RJ), Bulgarian substrain (Sofia SL222), Japan 172 strain (Tokyo 172-1), and BCG-Denmark 133.

BCG Vaccination Benefits For Infants

A study published by the BMJ in September 2025 concluded that in newborn babies weighing <2000 g in intensive care, BCG-OPV administered at a median age of 0.9 days reduced all-cause neonatal mortality, owing to a decrease in deaths from infections other than tuberculosis.

BCG Vaccine Alzheimer's Disease Dementia

On August 24, 2023, a systematic review and meta-analysis of BCG administration on the risk of dementia in bladder cancer patients found the pooled HR was 0.55 (0.42–0.73), indicating that BCG exposure or treatment reduced the risk of incident dementia by 45%. The JAMA Network published an Original Investigation on May 19, 2023, led by investigators at Massachusetts General Hospital and Brigham and Women's Hospital. The investigation concluded that the BCG vaccine was associated with a significantly lower rate and risk of Alzheimer's disease and related dementia in a cohort of patients with bladder cancer when accounting for death as a competing event. This phase 2 clinical trial is ongoing.

mini-review published on June 27, 2022, highlights how immune cells can mediate the relationship between BCG vaccination and AD, thereby supporting the health of the central nervous system. On February 22, 2022, MDPI published "BCG Vaccination and Plasma Amyloid: A Prospective, Pilot Study with Implications for Alzheimer's Disease," in which participants tended to have higher values of the Aβ42/Aβ40 ratio after receiving the BCG vaccine. On November 7, 2019, researchers at the Hadassah-Hebrew University Medical Centre collected the data of 1,371 people who had or had not received BCG as part of their treatment for bladder cancer. They found that just 2.4% of the patients treated with BCG developed Alzheimer's over the following eight years, compared with 8.9% of those not given the vaccine.

BCG Vaccine Bladder Cancer

The study of BCG anti-tumor activity began in 1929. Since 1977, BCG vaccination has been the standard therapy for treating high-risk nonmuscle-invasive bladder cancer (NMIBC) patients to avoid the recurrence and progression of the disease. BCG is the most common intravesical immunotherapy for treating early-stage bladder cancer, according to Cancer.org. BCG vaccination induces the recruitment and polarization of macrophages towards a pro-inflammatory phenotype, accompanied by the induction of the inflammatory cytokines TNF-α, IL-1β, and IL-6 in the tumor microenvironment. Macrophages directly induced apoptosis of human cancer cells through zebrafish TNF signaling.

Serum Institute of India's BCG vaccine is exported to Canada for immunotherapy to treat bladder cancer. In Australia, intravesical immunotherapy with BCG is approved. On April 22, 2024, the U.S. FDA approved the multi-dose ANKTIVA for BCG-unresponsive non-muscle Invasive Bladder Cancer. The End Drug Shortages Alliance confirmed in 2023 that about 20% of the organizations were not providing complete BCG vaccination routines to eligible cancer patients. When comparing BCG strains, the Tice stain showed a relatively high probability of recurrence compared with the Connaught (RR, 1.29; 95% CI 1.01–1.64) and RIVM (RR, 2.04; 95% CI 1.28–3.25) strains.

BCG Vaccine Diabetes

Various studies are investigating whether BCG vaccine therapy can enhance blood sugar control in Type 1 Diabetes by altering metabolism. In January 2023, PLOS ONE published the results of two observational studies. The epidemiological evidence analyzed here suggests that BCG may play a role in the prevention of type 1 diabetes (T1D) but does not support its role in preventing type 2 diabetes (T2D), most likely due to the interference of metformin. Our ecological analysis of global data suggests a potential role for neonatal BCG in preventing type 1 diabetes (T1D) and, to a lesser extent, type 2 diabetes (T2D). Researchers from Massachusetts General Hospital (MGH) presented positive updates in 2021 on their trials of the BCG vaccine, which aim to safely and significantly lower blood sugar levels. Over the course of three years, BCG restores the gene expression pattern of Tregs in type 1 diabetics to a pattern consistent with that of non-type one control subjects. In June 2018, an MGH research team published in npj Vaccines that three years after receiving two administrations of the BCG vaccine, four weeks apart, all members of a group of adults with longstanding type 1 diabetes showed an improvement in HbA1c to near-normal levels. This improvement persisted for the following five years.

BCG Vaccine Eczema

The Murdoch Children's Research Institute's initial study findings, published in the journal Allergy on August 24, 2021, showed that the BCG vaccine had a modest beneficial effect in preventing eczema in high-risk infants. However, a single dose of BCG-Denmark soon after birth could reduce the incidence of eczema in infants with two atopic parents.

BCG Vaccination Endometriosis

A mini-review published in 2021 addresses the possible use of BCG as a therapeutic for endometriosis, a syndrome of chronic pelvic pain due to ectopic growth of endometrial-type tissue outside of the uterine lining. The immune response to endometriosis reveals a complex balance between systemic pro-inflammatory immune activation and local anti-inflammatory characteristics that permit tumor growth. Lesions of endometriosis have an immune-cell-rich stroma with aberrant expression of pro- and anti-inflammatory cytokines, including IL-16, IL-18, and IL-1. BCG vaccination has been shown to alter the secretion of pro-inflammatory cytokines.

BCG Vaccine Herpes

The Lancet's eClinicalMedicine published results from a phase 3 clinical trial conducted across multiple countries on October 16, 2023, assessing the impact of BCG vaccination on recurrent herpes labialis. The study's results suggest that BCG-induced non-specific immune responses can enhance the body's immune response, particularly in males with a history of frequent recurrences. 

A systematic review of Medline, EMBASE, and PubMed in June 2020 identified 16 articles that were deemed relevant, comprising eight animal and eight human studies (301 patients). In nonrandomized human studies (that failed to control for a placebo effect), BCG vaccination appeared beneficial in 78% of adults with recurrent herpes genitalis or labialis, with 37% being recurrence-free for an extended period, 41% experiencing less frequent or severe episodes, and only 22% reporting no change. In the two studies on recurrent herpes labialis, 94% appeared to benefit from BCG. The one randomized controlled trial used an intervention in the control group with immunomodulatory effects, which limited its interpretation. In conclusion, the BCG vaccine is a readily available vaccine candidate that can help decrease diseases associated with HSV infection.

BCG Vaccine HIV

Coinfection with Mtb and HIV is a lethal combination, says the WHO. In sub-Saharan Africa, where HIV is most prevalent, the annual incidence of TB has risen to more than 300 cases per 100,000 inhabitants. In some of these places, nearly 50% of the HIV-infected population is coinfected with TB, and more than two-thirds of TB patients are infected with HIV. The lifetime risk of developing TB is as high as 30-50% for HIV-infected persons. In some parts of Southeast Asia, an estimated 20-25% of TB cases will be directly attributable to HIV, according to the WHO.

For neonates born to mothers with an unknown HIV status and neonates with an unknown HIV status born to HIV-infected mothers (regardless of their ART status), the WHO recommends BCG vaccination, as the benefits outweigh the risks. For a neonate confirmed by virologic testing to be positive for HIV, it is recommended that BCG vaccination be delayed until ART has been started.

Experts at Fred Hutchinson Cancer Center suggested in a study published in The Lancet HIV on October 11, 2022, that future TB vaccine development clinical trials should ensure people living with HIV have access to safe and effective TB vaccines.

On June 27, 2022, The Lancet Infectious Diseases published the results from a phase 2 study on HIV-infected children in South Africa. The researchers' Interpretation: The VPM1002 vaccine candidate was less reactive than BCG and was not associated with serious safety concerns. Both vaccines were immunogenic, with higher responses to the BCG vaccine.

In October 2020, the journal Nature published a BCG vaccine review that stated 'the potential TB vaccine candidates that can be exploited for use as a dual vaccine against TB/HIV copandemic (ii) progress made in the realm of TB/HIV dual vaccine candidates in a small animal model, NHP model, and human clinical trials the failures and promising targets for a successful vaccine strategy while delineating the correlates of vaccine-induced protection.'

BCG Vaccine Leprosy

Repeat BCG vaccination is standard practice in many countries to prevent Hansen's disease (leprosy). In 2018, the WHO included leprosy in its recommendation for single-dose BCG vaccination.

BCG Vaccine Liver Cancer Tumors

A study published in Advanced Science by UC Davis Health in February 2024 found that a dose of the BCG vaccine reduced liver tumor burden and extended the survival of mice with liver cancer. The study is the first to show BCG vaccinations as a potential treatment for hepatocellular carcinoma, a condition often associated with unfavorable treatment outcomes. Vaccination was characterized by a favorable safety profile and efficacy in inhibiting fibrosis, improving metabolism, and engaging trained immunity and T cells in therapeutic mechanisms.

BCG Vaccine Tuberculosis

Tuberculosis (TB) is a vaccine-preventable disease, says the WHO. A study titled "Efficacy of BCG Vaccine in the Prevention of Tuberculosis: Meta-analysis of the Published Literature" was published in 1994. On January 24, 2023, PLOS Medicine published a research article titled "The Cost and Cost-Effectiveness of Novel Tuberculosis Vaccines in Low- and Middle-Income Countries: A Modeling Study." Our analysis projected that an effective new TB vaccine could offer significant health and economic benefits from 2028 to 2050. The Lancet published an early-release survey on August 10, 2022 - Infant BCG vaccination and risk of pulmonary and extrapulmonary TB throughout the life course: a systematic review and individual participant data meta-analysis. Interpretation: Our results suggest that BCG vaccination at birth prevents tuberculosis in young children but is ineffective in adolescents and adults. Immunoprotection, therefore, needs to be boosted in older populations.

The WHO's Global Tuberculosis Report 2024 highlights mixed progress in the global fight against TB. While the number of TB-related deaths decreased from 1.32 million in 2022 to 1.25 million in 2023, the total number of people falling ill with TB rose slightly to an estimated 10.8 million in 2023.

BCG Vaccine Yellow Fever

The study demonstrated the effects of BCG vaccination on genome-wide histone modifications induced in trained monocytes. These modifications are associated with reduced yellow fever virus viremia levels due to increased IL-1β production and release.

BCG Vaccine for Children

BCG vaccination at birth or in infancy significantly reduces the risk of TB. The potential implications for child health are substantial, according to a study published in October 2020. For example, if BCG vaccination were given to children at birth, if higher measles vaccination coverage could be obtained, if diphtheria, tetanus, and pertussis-containing vaccines were not provided with or after the measles vaccine, or if the BCG strain with the best non-specific effects could be used consistently, then child mortality could be considerably lower. In 2005, all EU countries, including Andorra, Bulgaria, Norway, Romania, and Switzerland, participated in a survey on BCG vaccination in children

BCG Vaccine Pregnancy

BCG vaccination should not be given during pregnancy. However, no harmful effects on the fetus have been observed, and further studies are needed to prove its safety.

BCG Vaccine Dosage

In its thirteenth report, the WHO Expert Committee first considered establishing international requirements for the manufacture and control of the BCG vaccine in the context of Biological Standardization. Approved dose: BCG vaccine can be given either cutaneously or intradermally. Research is currently being conducted on respiratory administration, as humans' natural infection and sensitization to Mycobacterium tuberculosis typically occur in the respiratory system. The timing and dose of BCG vaccination were assessed by the 1995 Tuberculin Vaccination Survey (US FDA), Medline.gov, the U.K., 2020, and WHO. The intact vials of BCG VACCINE should be stored refrigerated at 2–8°C (36–46°F). This agent contains live bacteria and should be protected from direct exposure to the environment. When used to protect against TB, BCG is injected into the skin. Keep the vaccination area dry for 24 hours after receiving the vaccination, and keep it clean until the vaccination area is indistinguishable from the surrounding skin.

BCG Vaccine Side Effects

If you experience any unusual or severe symptoms after receiving this vaccine, tell your healthcare provider promptly or report them to the Vaccine Adverse Event Reporting System at www.vaers.hhs.gov.

BCG Vaccine United Kingdom

In the U.K. and various countries, BCG vaccination is administered to newborn infants at risk of TB. The WHO suggests that BCG programs for different age groups are equally effective against TB during puberty. BCG vaccines have effectively protected children against the rarer, severe forms of TB, such as TB meningitis. The Lancet Global Health published a study in September 2022 that found that BCG vaccination at birth protects against TB among children under five.

Public Health England (PHE) announced on July 27, 2021, that eligible babies should be offered the BCG vaccine at 28 days of age or soon after. BCG vaccination is recommended for babies up to 1 year old, and BCG vaccination may also be recommended for older children who have an increased risk of developing TB. On September 15, 2021, the U.K.'s PHE updated its fact sheet, which had previously been published in The Lancet on September 7, 2021, and in Cancer Immunology on June 24, 2022. Epidemiologist   Christine Stabell Benn and colleagues found (Mar. 2012) that BCG administered to children with low birth weight reduced all-cause mortality in these children by about 40% in the first year of life.

BCG Vaccine Price

UNICEF data show that the price awarded for the BCG vaccine per dose is nominal. The U.S. CDC Vaccine Price List was last updated in December 2022; many pharmacies in the U.S. charge over $100.00 for a single vial of BCG vaccines. According to various reports, the global TB Vaccine revenue is expected to increase by over 3% annually by 2027. Additional information on the BCG vaccine discount is posted at InstantRx™.

BCG Vaccine Clinical Trials

BCG is currently involved in active clinical trials covering various conditions. Click here to review the various ongoing clinical trials. 

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Availability: 
200 countries
Generic: 
Bacille Calmette-Guerin
Clinical Trial: 
https://clinicaltrials.gov/
Drug Class: 
Attenuated Vaccine
Condition: 
Last Reviewed: 
Friday, December 12, 2025 - 09:25
Brand: 
BCG
Abbreviation: 
BCG
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Yes
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Yes
Halal: 
Yes
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TG4001 HPV Cancer Vaccine

TG4001 HPV Vaccine Description

TG4001 is a therapeutic cancer vaccine candidate based on an attenuated and modified poxvirus (MVA) as a vector expressing the HPV16 E6 and E7 proteins (rendered non-oncogenic) interleukin-2, made by a type of T lymphocyte. TG4001 is developed in Human Papillomavirus (HPV)16 positive cancers, such as cervical, vaginal, and oropharyngeal squamous cell carcinoma of the head and neck. Transgene's myvac® is designed to stimulate and educate the patient's immune system to recognize and destroy tumors using their cancer-specific genetic mutations. 

On September 16, 2020, Transgene, previously known as Tipapkinogen Sovacivec, announced the analysis of the efficacy data from the Phase 1b/2 trial combining TG4001 with avelumab in HPV16-positive recurrent and/or metastatic malignancies showed promising clinical activity in the overall study population (34 evaluable patients).

Transgene announced on November 2, 2022, following an interim analysis of its randomized controlled Phase II clinical study comparing TG4001 in combination with avelumab to avelumab alone in patients with HPV16-positive anogenital tumors, the Independent Data Monitoring Committee has recommended the study continue. Based on positive signals observed in the interim analysis, the trial is expected to enroll an additional 66 patients for a total trial size of 120 patients compared to the previously announced target of 150 patients.

On June 5, 2023, the Company announced data from a phase 2 clinical trial found TG4001 could induce de novo immune responses against HPV16 antigens E6 and E7 in patients with advanced HPV16-positive anogenital cancers, and patients with complete objective response showed strong vaccine-induced immunoreactivity. Furthermore, Transgene announced on June 6, 2023, new immunological data assessed by tetramer staining confirms the induction of T cell responses in treated patients, all trial patients treated with TG4050 monotherapy continue to remain in remission to date. and Transgene and NEC are preparing a Phase II trial to further demonstrate the potential of TG4050 as an adjuvant treatment of head and neck cancer.

Transgene is a France-based clinical-stage biotechnology company that designs and develops novel immunotherapeutics.

TG4001 HPV Vaccine Indication

TG4001 is indicated to treat HPV16+ recurrent or metastatic malignancies, including oropharyngeal cancers. Therapeutic vaccines are active and targeted immunotherapeutics. According to the Company, they induce a cascade of immune reactions that produce T cells that will only destroy specific malignant cells.

TG4001 HPV Vaccine Dosage

Dosing levels are being evaluated in ongoing clinical trials. TG4001 is designed to have a two-pronged antiviral approach: to alert the immune system specifically to cells presenting the HPV16 E6 and E7 antigens found in HPV16-related tumors and to further stimulate the infection-clearing activity of the immune system through interleukin 2 (IL-2). 

TG4001 HPV Vaccine News

June 6, 2023 - Alessandro Riva, Chairman and CEO of Transgene, commented, "TG4050 has demonstrated its potential to extend patient remission after surgery and firmly establishes Transgene among the leading pioneers in the emerging field of individualized cancer vaccines. The monotherapy data we present at ASCO are a solid basis to accelerate the clinical development of this innovative therapy as an adjuvant treatment to HPV-negative head and neck carcinoma and potentially in other indications."

June 5, 2023 - Transgene announced that new data confirm the ability of this novel investigational therapeutic cancer vaccine to induce immune responses against HPV16 antigens that are associated with anti-tumor response.

November 2, 2022 - Hedi Ben Brahim, Chief Executive Officer of Transgene, stated: "The IDMC's recommendation to continue the study reinforces our confidence in TG4001, which follows promising data from our earlier Phase Ib/II trial. This also enables us to reduce the number of randomized patients in the trial. We look forward to completing this trial in H1 2024 and communicating its results when available."

June 24, 2021 - Transgene announced that the first patient had been enrolled in a randomized, controlled Phase II study evaluating the combination of TG4001 with avelumab versus avelumab monotherapy in patients with HPV16-positive anogenital tumors.

March 10, 2021 - Transgene announced the initial Phase Ib/II trial conducted in France and Spain had been amended to include a randomized comparison of TG4001 with avelumab versus avelumab monotherapy in anogenital cancers. The submission of the amended protocol has been initiated in Europe. Also, Transgene received US FDA clearance for the protocol under TG4001 IND. Patient enrollment is expected to start in Q2 2021. The trial will focus on patients with recurrent or metastatic HPV16-positive anogenital cancer without liver metastases, including cervical, vulvar, vaginal, penile, and anal cancer.

October 27, 2020 - Transgene is communicating the content of the late-breaking poster abstract that will be presented at the SITC 35th Anniversary Annual Meeting (SITC 2020), to be held virtually November 9-14, 2020. The combination of TG4001 and avelumab demonstrates anti-tumor activity (23.5% ORR) in patients with previously treated recurrent and/or metastatic HPV-related cancers. In addition, liver metastases profoundly impact outcomes regarding ORR and PFS. In patients without liver metastases, an ORR of 34.8% and a median PFS of 5.6 months were achieved.

October 19, 2020 - Transgene announced that detailed results of the data from the Phase 1b/2 trial combining TG4001 would be presented in a poster presentation at the upcoming virtual meeting of the Society for Immunotherapy of Cancer taking place November 9-14, 2020.

July 22, 2020 - Transgene performed a pooled analysis of the data from the Phase 1b/2 trial combining TG4001. This analysis confirms that TG4001 can be safely combined with an immune checkpoint inhibitor and shows the clinical activity of this combination regimen. The trial is being conducted in collaboration with Merck KGaA, Darmstadt, Germany, and Pfizer.

September 30, 2019 - Transgene presented promising safety and efficacy data of TG4001 in combination with avelumab (BAVENCIO®), a human anti-programmed death-ligand (PD-L1) antibody, in Human Papillomavirus (HPV) 16+ recurrent or metastatic malignancies, including oropharyngeal cancers.

April 4, 2019 - Study: Tipapkinogen Sovacivec therapeutic HPV vaccine's efficacy and safety in cervical intraepithelial neoplasia grades 2 and 3: Randomized controlled phase II trial with 2.5 years of follow-up.

TG4001 HPV Cancer Vaccine Clinical Trials

The Phase II study evaluates TG4001, an investigational therapeutic cancer vaccine, combined with avelumab compared to avelumab alone in patients with HPV16-positive anogenital tumors without liver metastases, through a continuing collaboration with the alliance of Merck KGaA, Darmstadt, Germany, and Pfizer, which is supplying avelumab.

Clinical Trial NCT03260023:  Phase Ib/II of TG4001 and Avelumab in HPV16 Positive R/M Cancers Including Oropharyngeal SCCHN.

Clinical Trial NCT01022346: A Study of RO5217790 in Participants With High-Grade Cervical Intraepithelial Neoplasia Associated With High-Risk Human Papillomavirus (HR-HPV) Infection (Completed).

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Availability: 
TBD
Generic: 
TG4001
Drug Class: 
Therapeutic Vaccine
Condition: 
Last Reviewed: 
Tuesday, June 6, 2023 - 13:55
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