About Conference
37th Annual Congress on Vaccine and Clinical Trials” during October 06-07, 2025 in Vancouver, Canada



Conference Series LLC LTD warmly welcomes you to the “37th Annual Congress on Vaccine and Clinical Trials” during October 06-07, 2025 in Vancouver, Canada. Where in most distinguished line up of eminent keynote speakers from around the globe will lead a dynamic scientific program of plenary sessions, symposia and hands-on workshops to share their expertise with our audience.
Advancing Vaccine Innovation: Bridging Research, Development, and Global Health " is the driving theme of the Vaccines Congress-2025, which will most definitely be reflected in the conference program, where we expect a remarkable turnout of world-renowned speakers.
Vaccines Congress-2025 will deliver new ideas, convictions, strategies and tactics to excel in the field of Vaccine and Clinical Trial. Vaccines Congress-2025 will offer an impressive roaster of keynote speakers, quality attendees, compelling content and concise reviews of the latest clinical advancements and guidance relating to the diagnosis and treatment of diseases including the use of new techniques.
Attendees at Vaccines Congress-2025 will have unique opportunity to meet with leaders of the Vaccine and Clinical Research profession from around the globe to discuss all of the scientific and technical breakthroughs that are changing the landscape of Clinical Research and fulfil their continuing education and professional development requirements.
Why to attend?
Vaccines Congress-2025 will be an excellent learning, sharing and networking platform for Immunologists and Virologists, Pharmaceutical Executives and Vaccine Manufacturers, Clinical Research Scientists and Clinical Trial Managers, Regulatory Affairs Professionals, Epidemiologists and Infectious Disease Specialists, Biotech Innovators and Entrepreneurs, Medical Doctors and Healthcare Providers, Academics and Research Professors, Global Health and NGO Representatives, Patients and Patient Advocacy Groups, Medical Journalists and Health Communicators, Funding Agencies and Investors, Clinical Trial Participants and Volunteers and of course the most important Students, our future. from the Asia-Pacific region and beyond. It will provide continuing education opportunities as well as world-class scientific content delivered by quality keynote speakers, with plenary sessions, symposia, hands-on workshops, and exhibition. Conference Series LLC Ltd organizes a conference series LLC Ltd of 1000+ Global Events inclusive of 300+Conferences, 500+ Upcoming and Previous Symposiums and Workshops in USA, Europe & Asia with support from 1000 more Scientific Societies and Publishes 700+ Open Access Journals which contains over 30000 eminent personalities, reputed scientists as editorial board members.
What’s New?
Vaccines Congress-2025 includes international attendee workshops, lectures, and symposia, including a designated registration area, a refreshment break, and gala lunch. Vaccine and Clinical Researcher can join the Conference series LLC Ltd as an international member to receive discounts on registration. So come and join leading experts and allied professionals from October 06-07, 2025 in Vancouver, Canada to keep up with the rapidly accelerating pace of change that is already having an impact on the field of Clinical Research and will continue to in the future.
Potential Participants
Vaccines Congress-2025 invites participants from all leading clinics, universities, clinical research institutions and Vaccine production companies to share their research experiences on all aspects of this rapidly expanding stream and thereby, providing a showcase of the latest research and provide a better health care to the world. It is also designed for practicing Clinical Research Coordinator, Clinical Research Associate, Physicians in training and other healthcare professionals interested in the latest advances and techniques in the field.
Abstract submission:
Abstracts should contain 250-300 words and can submit online. Speakers can choose the topic from our scientific sessions or any research work in the related field. Abstracts will be published in our peer reviewed journals.
https://vaccines.conferenceseries.com/abstract-submission.php
Session and Tracks
Track 1: Vaccine and Vaccination
A vaccination is a biological agent that aims to provide immunity without actually causing the disease by encouraging the body's immune system to identify and combat particular invaders (such bacteria or viruses).Vaccines include genetic material that tells the body to make a harmless portion of the pathogen (such a protein) or weakened, inactivated, or fragments of germs.After being exposed, the immune system reacts by creating memory cells and antibodies, which enables the body to react more quickly and efficiently the next time.
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In order to "train" your immune system, vaccines
Replicating an infection (but without being infected).
Triggering the production of memory cells and antibodies as part of an immune response.
Preparing the body to more successfully combat the actual infection in the future.
Innovation in Vaccines Using AI and Tech
According to an ArXiv review, AI and deep learning are transforming the production of vaccines, from immune response prediction to epitope selection, potentially substituting animal models and speeding up trials.
Global pandemic preparedness and AI: More extensive AI-powered monitoring systems have been suggested to detect and address disease outbreaks.
Track 2: The COVID-19 vaccine's next-generation RNA platforms and mRNA
A respiratory disease that spreads easily, COVID-19 is brought on by the SARS-CoV-2 virus.7 million+ deaths and over 770 million confirmed cases globally (as of 2025).Worldwide disturbances in the fields of education, the economy, society, and mental health. Hastened the development of telemedicine, vaccination platforms, and digital healthcare. The quickest vaccine development in history, utilizing both conventional and next-generation technology, was spurred by COVID-19. Training the immune system to identify and combat SARS-CoV-2, especially its spike (S) protein, is the primary objective of all vaccinations.The COVID-19 vaccines still mostly use conventional mRNA, with advancements such as superior lipid nanoparticles (LNPs) for improved durability and delivery.Currently utilized in boosters such as Arcturus's.ARCT-154, self-amplifying RNA (saRNA) multiplies within cells to increase antigen expression at lower doses.Although still in its infancy, circular RNA (circRNA) offers additional stability and sustained protein synthesis.
mRNA Vaccines
mRNA vaccines, developed by Pfizer-BioNTech and Moderna, use messenger RNA to train the immune system by producing a harmless spike protein from viruses like SARS-CoV-2. This method is safe and efficient, preparing the immune system for future exposure. mRNA vaccines have significantly impacted the COVID-19 pandemic and are being researched for other diseases.
Viral Vector Vaccines
Viral vector vaccines use a harmless virus to introduce a gene encoding a spike protein of a target virus into human cells. This genetic instruction triggers the immune system to recognize and fight the virus. Examples include Oxford-AstraZeneca, Johnson & Johnson, and Sputnik V, used during COVID-19.
Inactivated Virus Vaccines
Inactivated virus vaccines are non-infectious whole viruses killed or inactivated through heat or chemical treatment. They still carry viral components, allowing the immune system to recognize and respond. Examples include COVID-19 vaccines like Covaxin, CoronaVac, and BBIBP-CorV, used in global immunization programs.
Protein Subunit Vaccines
Protein subunit vaccines use purified virus fragments, like the spike protein or a fragment, to stimulate an immune response. These vaccines are highly targeted and safe, focusing the immune system on recognizing and neutralizing specific parts of the virus. Key examples include Novavax and Anhui Zhifei.
DNA Vaccines (Emerging Tech)
DNA vaccines use plasmids containing genetic instructions to produce a spike protein for viruses like SARS-CoV-2. These stable, needle-free, and non-live virus vaccines stimulate the immune system to fight future infections. The world's first DNA vaccine, ZyCoV-D, is an example of this innovative technology.
Track 3: VACCINES FOR CANCER
Uncontrolled proliferation and spread of aberrant cells within the body is a symptom of a group of disorders known as cancer. It can be fatal if the spread is not stopped. It can impact nearly any organ or tissue. Environmental exposures or genetic alterations are typically the cause of cancer. It can be multifaceted, combining environmental, lifestyle, and hereditary variables. One type of immunotherapy that aids the body's immune system in identifying and combating cancer cells is the cancer vaccination. Cancer vaccines, in contrast to conventional vaccines that prevent infections, can either treat pre-existing malignancies (therapeutic vaccines) or prevent specific cancers (prophylactic vaccines).Therapeutic vaccines are demonstrating increasing promise, especially when customized and used in conjunction with other immunotherapies, even though preventive vaccines have already demonstrated benefit in avoiding virus-related malignancies. The goal of ongoing research is to increase the accessibility, effectiveness, and delivery of vaccines.
Vaccines for prophylactic (preventive) cancer
Prophylactic (preventive) cancer vaccines are designed to protect the body against viruses that are known to cause certain types of cancer, thereby reducing the risk of cancer development. A key example is the Human Papillomavirus (HPV) vaccine, such as Gardasil or Cervarix, which protects against HPV infection—a major cause of cervical, anal, and throat (oropharyngeal) cancers. Another important example is the Hepatitis B vaccine, which guards against the Hepatitis B virus (HBV), significantly lowering the risk of liver cancer (hepatocellular carcinoma). By preventing these viral infections, these vaccines play a critical role in reducing cancer incidence worldwide.
Medicinal Vaccines for Cancer Treatment
Therapeutic cancer vaccines aim to treat existing cancers by stimulating the immune system to recognize and attack cancer cells. Unlike preventive vaccines, these are designed for patients who already have cancer. One example is Sipuleucel-T (Provenge), which is approved for advanced prostate cancer. It is created by collecting a patient’s immune cells, modifying them to better target cancer cells, and then reinfusing them into the patient. In addition to approved treatments, several experimental cancer vaccines are currently being tested in clinical trials for cancers such as melanoma, lung cancer, glioblastoma, and pancreatic cancer. These therapies represent a promising area of research in personalized and immune-based cancer treatment.
Current Developments
mRNA cancer vaccines are a type of personalized immunotherapy designed to target mutations specific to an individual’s cancer. These vaccines use messenger RNA (mRNA) to instruct the immune system to recognize and attack cancer cells based on unique tumor mutations. Companies like BioNTech and Moderna are actively conducting clinical trials in this area. A key focus of mRNA cancer vaccines is on neoantigens—mutations found only in cancer cells and not in normal, healthy cells—making them ideal targets for a precise immune response. To enhance effectiveness, these vaccines are often combined with checkpoint inhibitors, such as anti-PD-1 or anti-PD-L1 therapies, which help overcome immune resistance and boost the body's ability to fight cancer. This combination approach is showing promising results in early clinical studies.
Track 4: Toxoid vaccination
A toxoid vaccine is a type of immunization that protects against bacterial diseases caused by toxins—poisonous substances produced by certain bacteria. These vaccines are made from toxins that have been inactivated, usually using formalin (a chemical method) or heat. The inactivated toxin, called a toxoid, loses its toxic effect but still retains its antigenic properties, meaning it can trigger an immune response. When administered, the immune system recognizes the toxoid as foreign and produces specific antibodies against it. If the person is later exposed to the actual toxin-producing bacteria, these antibodies will neutralize the toxin, preventing illness.
In recent years, toxoid vaccines have seen several notable advancements. First, improved combination vaccines like pentavalent (5-in-1) and hexavalent (6-in-1) formulations have been developed, incorporating Diphtheria, Tetanus, and Pertussis toxoids along with other antigens like Hepatitis B, Hib, and Polio. These are now widely used in Universal Immunization Programs (UIPs) around the world to simplify dosing schedules and improve public trust. Second, global campaigns led by WHO have resulted in the elimination of neonatal tetanus in over 80 countries, thanks to widespread use of maternal Td vaccines. Third, Tetanus-Diphtheria (Td) booster doses are now standard for adolescents and adults every 10 years, especially for wound care and travelers.
Research is also ongoing into novel adjuvants to improve immune responses to toxoid vaccines, especially in older adults, using agents like aluminum salts and TLR agonists. Another breakthrough is the development of thermostable toxoid formulations, which allow vaccines to be stored and used in hot or remote areas without refrigeration. Additionally, experimental studies are exploring nanoparticle-based delivery systems for tetanus and diphtheria toxoids, aiming to reduce side effects and enable needle-free administration. These developments reflect the growing potential of toxoid vaccines in improving global public health through more accessible, effective, and safer immunization.
Track 5: DNA, RNA & SYNTHETIC VACCINES
To structure antibodies against an organism, researchers employ a variety of techniques. These choices are frequently based on important information about the microbe, such as how it contaminates cells and how the immune system responds to it, as well as practical considerations, such as the areas of the body where the antibody would be used. A solid neutralizer reaction to the free-gliding antigen released by cells would be triggered by a DNA and RNA vaccination against a bacterium, and an antibody would also stimulate a solid cell reaction against the microbial antigens shown on cell surfaces. Since the DNA and RNA antibodies would only include copies of a few of the creature's characteristics rather than the actual organism itself, it could not cause the disease. Additionally, designing and producing DNA antibodies is reasonably easy and inexpensive. Whole illnesses, microbes, or parts of both can be used to create inactivated vaccines. Fragmentary antibodies can be based on polysaccharides or proteins.
Track 6: Antinatal vaccinations
Pregnancy-related vaccinations may protect both the expectant mother and the unborn child from antibody-preventable illnesses. Due to the fact that their immune system has not fully developed, newborns are at a significant risk of suffering from severe illnesses and dying from some fatal diseases. One goal of immunizing expectant mothers is to increase the amount of maternal counteracting agents—proteins that fight disease—transmitted to the unborn child, potentially protecting them from unstoppable infection.
Track 7: Vaccines against non-traditional illnesses
Seeing how drug designers work in the immune response zone to coordinate vaccinations against non-irresistible illnesses and some odd symptoms is fascinating. To date, the majority of these vaccinations have developed into therapy antibodies. This is the opposite of antibodies against infectious diseases that are used as preventative vaccinations. Despite some very persistent disappointments and hopeful late-stage up-and-comers, there is still no immune response that prompts antibody affirmed focused on antigens other than microorganisms (i.e., self-antigens, enslaved particle antigens, and others). Examining the work of drug engineers in the field of immune response actuation of antibodies coordinated against non-irresistible diseases and some erratic illnesses is fascinating.
Track 8: Creation and development of vaccines
The development of vaccinations focuses on a range of mechanical operations and applied research that enhance and promote better frameworks and procedures for antibody health. The unusual Ebola outbreak last year sparked business and research response, and as we continue to hunt for solutions, we should review the lessons learnt to overcome and flow challenges. Antibody improvement is a drawn-out, intricate process that often takes ten to fifteen years and involves both private and public participation. The current system for developing, evaluating, and overseeing vaccines was established in the 20th century when the organizations involved formalized their plans and policies.
Track 9: Vaccine for infectious illnesses in humans
About 25% of deaths globally are attributed to irreversible illnesses, especially in children younger than five. The establishment of appropriate mechanisms to ensure that all children get access to basic antibodies, regardless of geographic location or socioeconomic background, could significantly reduce the burden of incurable diseases. Additionally, new safe and effective vaccines should be developed for a variety of illnesses for which there is now no effective preventative intervention strategy available or practical. To ensure that these novel or enhanced antibodies are fully developed and made available to the underprivileged populations as quickly as possible, the public, commercial, and humanitarian sectors must work together.
Track 10: Conjugated and combination vaccinations
More illnesses are becoming prevented using antibodies, yet network and supplier acknowledgment needs are being met without increasing the number of infusions. Blend conjugate antibodies are indicative of an important and unavoidable development. The sufficiency and security of mix conjugate antibodies are examined in this work, along with the function of immunological memory, covert collaboration between vaccination epitopes, and invulnerability relationships. Specifically, the role of mix antibodies against Neisseria meningitidis, Streptococcus pneumonia, and Haemophilus influenza type b is discussed. Key areas for additional research are identified, the implications of these findings for different networks are analyzed, and recommendations for post-licensure checking are addressed.
Track 11: Vaccine efficiency and well-being
Antibody adequacy refers to the ability of vaccinations to provide the suggested beneficial outcomes for vaccinated individuals in a defined population under ideal conditions of use. The potential benefits of a successful vaccination, such as improved health and prosperity and protection against disease and its effects on the body, mind, and finances, must be balanced against the risk of an adverse event after vaccination (AEFI). The possibility of an adverse or unwanted outcome occurring, as well as the severity of the ensuing harm to the health of those who have been vaccinated in a described population after receiving an immunization under ideal conditions of use, are known as antibody-related hazards.
Track 12: Zika Virus vaccines
The disease caused by the Zika virus is addressed by the Live-Attenuated antibody. The antibody's monovalent form is intended to prevent Zika infection contamination. The Zika virus belongs to the same genus as flavivirus, which is spread by Aedes mosquitoes. Understanding the structure of flavivirus molecules, the significance of E dimers as the primary antigenic target, and a thorough understanding of balancing tools all contribute to the development of immunity.
Track 13: HIV , Malaria & TB vaccines
HIV is a virus that targets the body's defenses against infections, particularly the CD4 (T-helper) cells. HIV can cause AIDS (Acquired Immunodeficiency Syndrome), a late-stage immune weakness, if treatment is not received. Although HIV is still a serious worldwide health concern, preventative and treatment methods have greatly improved. People can lead normal lives with ART.There is hope for stopping transmission with PrEP, PEP, and new vaccinations. A long-term functional treatment and a prophylactic vaccine are still being researched. Malaria continues to guarantee an estimated 2 to 3 million deaths annually and to cause unimaginable misery for the 300 to 500 million people who are infected each year. Due in large part to the expansion of drug-safe parasite strains, the decay of the medical services system, and difficulties in implementing and maintaining vector control programs in many developing countries, jungle fever is considered a reemerging disease. Plasmodium falciparum, Plasmodium vivax, Plasmodium malaria, and Plasmodium ovale are the four protozoan parasites that cause jungle fever in humans. Most deaths and the great majority of severe illnesses, including cerebral jungle fever, are caused by P. falciparum. Two billion people who are dormant with M.tuberculosis 5–10% of infected people develop illness. 9 million new cases of tuberculosis each year.Each year, 1.5 million TB deaths occur equivalent to twenty passenger aircraft crashes each day. Adults suffering from citatory illness can spread tuberculosis. HIV-positive people worry about more serious health issues. Compared to more experienced children and adults, there was a significantly higher risk of progression from TB infection to active infection, as well as a significantly higher rate of TB morbidity and mortality.
Track 14: rDNA technology in vaccine development
In order to create a new genetic sequence that may be introduced into host cells (such as bacteria, yeast, or mammalian cells) to make particular proteins—typically antigens used in vaccines—recombinant DNA (rDNA) technology combines DNA from several organisms. This method, which is fundamental to contemporary biotechnology, enables researchers to develop tailored, safe, and efficient vaccinations without utilizing whole pathogens.
Recent Developments (2023–2025)
Recent vaccine technology advancements use recombinant DNA methods to create targeted, effective vaccines against challenging diseases. For malaria, R21/Matrix-M fused CSP with Hepatitis B virus surface antigen. For influenza, researchers are developing a universal flu vaccine using conserved regions of hemagglutinin stem protein. Next-generation HPV vaccines target a wider range.
Track 15: Adverse reactions to the vaccination
Before being approved for clinical usage, anti-infection medicines are tested for adverse responses. Depending on the type of antimicrobial used, the organisms being treated, and the patient, certain antitoxins cause mild to severe side effects. Immunizations usually cause less harmful side effects, such as mild fever, migraine, muscle and joint pain, shaking, and so on, but almost no antibodies cause rare symptoms, such as hypersensitivity, or anaphylactic reaction.
Track 16: Vaccine manufacturing technologies
Vaccine manufacturing uses advanced technologies like live attenuated and inactivated vaccines, subunit and recombinant protein vaccines, viral vector vaccines, mRNA vaccines, and DNA vaccines. Traditional methods involve weakened pathogens, while biotechnology advancements have led to subunit and recombinant protein vaccines, viral vector vaccines, mRNA vaccines, and DNA vaccines. Innovations like single-use bioreactors, continuous manufacturing, thermostable, formulations, and nanoparticle delivery systems improve vaccine production speed and stability.
Track 17: Vaccine Research and Clinical trials
Vaccination plays an increasingly important role in maintaining our health throughout our lives. Novel antibody structures have yielded both successes and setbacks in recent years, and the value of iterative approaches is increasingly recognized. Because of the highly advanced tools for avoiding diseases for which there are now no antibodies, vaccine development continues to be tested. In order to expedite antibody planning, these combine the preclinical discovery of novel antigens, adjuvants, and vectors with computer analyses of clinical data. Before being approved, each epic immunization candidate needs be evaluated for security, immunogenicity, and defensive adequacy in humans.
Track 18: Recent advances in vaccine development
With the rise in popularity of mRNA technology, DNA vaccines, viral vector vaccines, recombinant protein vaccines, and virus-like particles, vaccine development has changed dramatically in recent years. To forecast antigens and create potential vaccines, artificial intelligence and machine learning are employed. Self-amplifying RNA (saRNA) vaccines are being produced for lower doses, and universal vaccinations are being created for numerous viral strains. Hepatitis B, HIV, and cancer are among the illnesses for which therapeutic vaccinations are now being developed. Additionally being investigated are adjuvants, modular platforms, reverse vaccinology, and better vaccine delivery techniques. These patterns show a move toward vaccinations that are more intelligent, quicker, and more focused.