Skip to content
Clinical Trials – home

Understanding the Pneumococcal Polysaccharide Serotype 6B Vaccine

Pneumococcal Polysaccharide Serotype 6B is an investigational medicinal product. No trial currently registered in Europe lists it – that can change as new trials are authorised, and it may be under study elsewhere.

In short

This article summarizes several clinical trials investigating the use of pneumococcal polysaccharide serotype 6B conjugate vaccine. These trials aim to evaluate the safety, tolerability, and immune responses elicited by various pneumococcal conjugate vaccine formulations containing serotype 6B, either alone or in combination with other serotypes. The studies involve different populations, including healthy adults, children, and those at increased risk of pneumococcal disease.

What is Pneumococcal Polysaccharide Serotype 6B?

Pneumococcal polysaccharide serotype 6B is a component of several pneumococcal vaccines. It is one of many serotypes (variants) of the bacterium Streptococcus pneumoniae, also known as pneumococcus. This bacterium can cause various infections, including pneumonia, meningitis, and bloodstream infections.

Pneumococcal disease refers to any infection caused by Streptococcus pneumoniae bacteria. These infections can range from mild to severe and can be life-threatening, especially in young children, older adults, and people with weakened immune systems.

How the Vaccine Works

The pneumococcal polysaccharide serotype 6B vaccine works by stimulating your immune system to produce antibodies against this specific type of pneumococcal bacteria. When the vaccine is injected, your body recognizes the inactivated bacterial components as foreign and creates antibodies to fight them. This prepares your immune system to respond quickly if you're ever exposed to the actual bacteria in the future.

In many pneumococcal vaccines, the serotype 6B component is conjugated to a carrier protein. This means it's chemically linked to another protein, which helps enhance the immune response, especially in young children. Common carrier proteins include CRM197 (a non-toxic variant of diphtheria toxin) and protein D (derived from non-typeable Haemophilus influenzae).

Who Needs This Vaccine?

Pneumococcal vaccines containing serotype 6B are recommended for several groups:

  • Infants and young children as part of their routine vaccination schedule
  • Adults 65 years and older
  • People with certain medical conditions that increase their risk of pneumococcal disease, such as:
    • Chronic heart, lung, or liver disease
    • Diabetes
    • Weakened immune systems
    • Cochlear implants or cerebrospinal fluid leaks

Your healthcare provider can advise you on whether you need this vaccine based on your age, health status, and vaccination history.

How is it Administered?

The pneumococcal polysaccharide serotype 6B vaccine is typically administered as an intramuscular injection, usually in the upper arm for adults or the thigh for infants. It's often given as part of a combination vaccine that protects against multiple pneumococcal serotypes.

The number of doses and timing can vary depending on the specific vaccine and the person's age and health status. For example, infants might receive a series of doses as part of their routine vaccinations, while adults might only need a single dose or a booster after several years.

Safety and Side Effects

Pneumococcal vaccines containing serotype 6B have been extensively studied and are generally considered safe. Like all vaccines, they can cause some side effects, but serious reactions are rare. Common side effects may include:

  • Pain, redness, or swelling at the injection site
  • Mild fever
  • Fatigue
  • Muscle aches

These side effects usually resolve within a few days. Severe allergic reactions are very rare but can occur with any vaccine. If you experience any severe symptoms after vaccination, seek medical attention immediately.

Effectiveness

Pneumococcal vaccines that include serotype 6B have been shown to be effective in reducing the incidence of invasive pneumococcal disease caused by this serotype. The effectiveness can vary depending on factors such as age, overall health, and the specific vaccine used.

It's important to note that while the vaccine provides protection against serotype 6B and other included serotypes, it doesn't protect against all types of pneumococcal bacteria. However, by protecting against common and often more severe serotypes, these vaccines significantly reduce the overall risk of pneumococcal disease.

Ongoing Research

Researchers continue to study pneumococcal vaccines to improve their effectiveness and broaden their coverage. Some areas of ongoing research include:

  • Developing vaccines that protect against more serotypes
  • Improving vaccine effectiveness in specific populations, such as the elderly or immunocompromised individuals
  • Studying the long-term effectiveness and need for booster doses
  • Monitoring the impact of vaccination on pneumococcal disease rates and potential changes in circulating serotypes

These ongoing studies help ensure that pneumococcal vaccines, including those containing serotype 6B, continue to provide optimal protection against pneumococcal disease.

Questions people often ask

Clinical Trials Concierge

Prefer not to search? Our Concierge searches the trials for you.

Tell us about your condition – we search every trial in Europe and connect you with the right site.

Legal notice · Published by CTIN POLAND sp. z o.o., ul. rtm. Witolda Pileckiego 67/109, 02-781 Warsaw, Poland · KRS 0001111334 · REGON 528919042 · NIP 9512598637

© 2026 Clinical Trials EU – European Clinical Trials Information Network

GDPR compliance, ISO 9001 and ISO 27001 certified (LL-C Certification)

On this site, “treatment” means an investigational medicine being studied in a clinical trial. Its safety and efficacy for the use being studied have not yet been confirmed, some participants may receive a placebo or a comparator medicine, and taking part does not guarantee any health benefit. The decision to take part is made by the doctor at the research site. This site is for information only and does not replace medical advice.

This service is not affiliated with the European Commission, the EMA, or the official CTIS system. Most information comes from publicly available international clinical-trial registries, supplemented by data from academic sites, national regulators and commercial sponsors. On this site, “treatment” and “therapy” mean a medicine being tested in a clinical trial. Its safety and effectiveness in the use being studied are not yet confirmed, some participants may receive a placebo or a comparator, and taking part does not guarantee a health benefit. The doctor at the research site decides who can take part. This site provides information, not medical advice. Certain content and visual elements on this website have been generated or enhanced using artificial intelligence (AI).