VIMKUNYA:
The first and only
virus-like particle
vaccine for chikungunya1,2

A group of travelers of various ages stands together in a forest, where mosquito protection is recommended
A group of travelers of various ages stands together in a forest, where mosquito protection is recommended
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The FIRST virus-like particle
(VLP) vaccine
indicated to
help prevent chikungunya1,2

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Mostly mild to moderate adverse reactions

In clinical studies, the most common adverse reactions in people 12–64 years old were injection site pain (23.7%), fatigue (19.9%), headache (18.0%), and myalgia (17.6%). In people 65 and older, the most common adverse reactions were injection site pain (5.4%), myalgia (6.3%), and fatigue (6.3%)1

White circle with white texting reading 3 weeks

Almost everyone had
a
seroresponse by
3 weeks

98% of people ages 12–64
and 87% of those 65+1,*

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APPROVED for ages 12 and over1

*Among adults and adolescents aged 12–64, 97.8% achieved a seroresponse at Day 22 with VIMKUNYA, vs 1.2% with placebo. Among
people aged ≥65, 87.3% achieved a seroresponse at Day 22 with VIMKUNYA, vs 1.1% with placebo.1

CHIKUNGUNYA:
NOW REPORTED
IN 110+ COUNTRIES3,4

About 500,000 cases of chikungunya—including over 400 deaths—were recorded worldwide in 2023.5

Know the
at-risk areas
Report Map
Report Map
under-map-circles

Regions that have reported chikungunya cases according to the World Health Organization, 20206

Preventing a debilitating
viral disease7

Chikungunya virus (CHIKV) is one of the most common viral diseases spread by mosquitoes8 and can lead to painful symptoms in over 75% of people who become infected.9,10 So it's important to take steps to take on chikungunya.

Learn more
about the risks
  • 3 OUT OF 4

    people infected with CHIKV get symptoms,† like severe joint pain, fever, and headache.9

  • 2 OUT OF 5

    can have chronic symptoms, like joint pain, that last for months or years.9,11,‡

†In a systematic literature review, meta-analysis of 8 studies determined that the overall symptomatic rate of chikungunya infection was 75% (n=912/1217; 95% CI, 0.63-0.84).9

‡Including a meta-analysis of 34 studies across 15 countries showing that more than 40% of patients developed severe long-term symptoms, lasting for months.11

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Video Transcript

You see every type of traveller.

A team of travellers united under one thing – your protection against chikungunya, a mosquito-borne disease.

And with VIMKUNYA, you can help protect a range of people from becoming infected with chikungunya.

VIMKUNYA is a vaccine indicated for prevention of disease caused by chikungunya virus in individuals 12 years of age and older.

VIMKUNYA is approved under accelerated approval based on anti-chikungunya virus neutralizing antibody levels.

Confirmatory trials are required.

Do not administer VIMKUNYA to individuals with a history of a severe allergic reaction (anaphylaxis) to any of its components.

Appropriate medical treatment must be immediately available to manage potential anaphylactic reactions.

Immunocompromised individuals, including individuals receiving immunosuppressive therapy may have a diminished immune response to VIMKUNYA.

Syncope (fainting) may occur.

Procedures should be in place to avoid injury.

The most common solicited adverse reactions in individuals aged 12 to 64 (greater than 10%) were injection site pain, fatigue, headache, and myalgia.

And in individuals 65 and older (greater than 5%) were injection site pain, myalgia and fatigue.

VIMKUNYA is a virus-like particle (VLP) vaccine, which means it’s designed to mimic the chikungunya virus without causing disease.

VIMKUNYA induced a robust seroresponse within 3 weeks after vaccination.

So, are your patients ready to face chikungunya?

VIMKUNYA, let’s go.

Please see full Prescribing Information via the link on-screen.

Watch the
latest video

See how you can help your patients protect themselves from chikungunya when they travel.1

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US healthcare professional?

Indications and Usage

VIMKUNYA is a vaccine indicated for the prevention of disease caused by chikungunya virus in individuals 12 years of age and older. The indication is approved under accelerated approval based on anti-chikungunya virus neutralizing antibody levels. Continued approval for this indication may be contingent upon verification of clinical benefit in a confirmatory trial.

Important Safety Information

Contraindications

Do not administer VIMKUNYA to individuals with a history of a severe allergic reaction (e.g., anaphylaxis) to any component of the vaccine.

Warnings and Precautions


Adverse Reactions

In clinical studies, the most common solicited adverse reactions (>10%) in individuals 12 through 64 years of age were pain at the injection site (23.7%), fatigue (19.9%), headache (18%), and myalgia (17.6%). The most commonly reported solicited adverse reactions (>5%) in individuals 65 years of age and older were injection site pain (5.4%), myalgia (6.3%), and fatigue (6.3%).

Use in Specific Populations

There are no clinical studies of VIMKUNYA in pregnant individuals.

To report SUSPECTED ADVERSE REACTIONS, contact Bavarian Nordic Inc. at
1-833-365-9596 or drug.safety@bavarian-nordic.com or VAERS at 1-800-822-7967 or www.vaers.hhs.gov.

Please see full Prescribing Information here.

References

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Indications and Usage

VIMKUNYA is a vaccine indicated for the prevention of disease caused by chikungunya virus in individuals 12 years of age and older. The indication is approved under accelerated approval based on anti-chikungunya virus neutralizing antibody levels. Continued approval for this indication may be contingent upon verification of clinical benefit in a confirmatory trial.

Important Safety Information

Contraindications

Do not administer VIMKUNYA to individuals with a history of a severe allergic reaction (e.g., anaphylaxis) to any component of the vaccine.

Warnings and Precautions

  • Appropriate medical treatment must be immediately available to manage potential anaphylactic reactions.
  • Immunocompromised individuals, including individuals receiving immunosuppressive therapy, may have a diminished immune response to VIMKUNYA.
  • Syncope (fainting) may occur in association with administration of injectable vaccines including VIMKUNYA. Procedures should be in place to avoid injury from fainting.

Adverse Reactions

In clinical studies, the most common solicited adverse reactions (>10%) in individuals 12 through 64 years of age were pain at the injection site (23.7%), fatigue (19.9%), headache (18%), and myalgia (17.6%). The most commonly reported solicited adverse reactions (>5%) in individuals 65 years of age and older were injection site pain (5.4%), myalgia (6.3%), and fatigue (6.3%).

Use in Specific Populations

There are no clinical studies of VIMKUNYA in pregnant individuals.

To report SUSPECTED ADVERSE REACTIONS, contact Bavarian Nordic Inc. at
1-833-365-9596 or drug.safety@bavarian-nordic.com or VAERS at 1-800-822-7967 or www.vaers.hhs.gov.

Please see full Prescribing Information here.

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