Actor Portrayal

A PCV specifically designed for adults that helps protect against the serotypes responsible for the most cases of adult IPD1,2,a

THAT’S BRILLIANT DESIGN

~54% Covered by PCV20 vs ~82% Covered by CAPVAXIVE

% of IPD cases in adults 50+ covered by vaccine serotypes

CAPVAXIVE is the only FDA-approved pneumococcal conjugate vaccine that helps protect against serotypes responsible for ~82% of invasive pneumococcal disease cases in adults 50 years or older, compared to ~54% by PCV20 on a national level.1,2,a Learn more >>

Intentional serotype selection1,2,b

11 serotypes in CAPVAXIVE
that are not covered by PCV20 cause
~37% of IPD cases
in adults 50 years or older at a national level.

These values are based on CDC epidemiologic data and do not reflect the efficacy of the respective vaccines.2 There are currently no studies comparing the efficacy of CAPVAXIVE and PCV20.

CDC recommendations

Dosing and administration

Reimbursement

CDC recommendations: updated October 20243

CAPVAXIVE PCV Recommendations From the CDC for Vaccine Naïve and Previously Vaccinated Adults Ages 19-49 and 50+CAPVAXIVE PCV Recommendations From the CDC for Vaccine Naïve and Previously Vaccinated Adults Ages 19-49 and 50+

 *Routine if PCV13 was administered at any age and PPSV23 was administered before age 65 with the last pneumococcal vaccine being at least 5 years prior. Shared clinical decision-making if PCV13 was administered at any age and PPSV23 was administered at or after the age of 65 and the last pneumococcal vaccine was at least 5 years prior.3

 Certain chronic medical conditions (eg, diabetes, chronic heart disease, chronic lung disease, or chronic liver disease) or behavioral risk factors (eg, smoking or alcoholism).3

 See ACIP recommendations for full list of immunocompromising conditions, including HIV.3

 §Also applies to patients with certain immunocompromising conditions who have received PCV13 followed by 2 doses of PPSV23.3

Are my adult patients at risk?

Share with health care professionals

aBased on CDC ABC surveillance data from the years 2019–2023, representing ~35 million persons and 10 states across the US. Regional variations may exist.2,3,5-9

bPCV20 serotypes for IPD case coverage: 1, 3, 4, 5, 6A, 6B, 7F, 8, 9V, 10A, 11A, 12F, 14, 15B, 18C, 19A, 19F, 22F, 23F, and 33F.10

CAPVAXIVE serotypes for IPD case coverage: 3, 6A, 7F, 8, 9N, 10A, 11A, 12F, 15A, 15B, 15C, 16F, 17F, 19A, 20A, 22F, 23A, 23B, 24F, 31, 33F, and 35B.

ABC, Active Bacterial Core; ACIP, Advisory Committee on Immunization Practices; CDC, Centers for Disease Control and Prevention; CSF, cerebrospinal fluid; FDA, Food and Drug Administration; HIV, human immunodeficiency virus; IPD, invasive pneumococcal disease; PCV, pneumococcal conjugate vaccine; PCV13, 13-valent pneumococcal conjugate vaccine; PCV15, 15-valent pneumococcal conjugate vaccine; PCV20, 20-valent pneumococcal conjugate vaccine; PPSV23, 23-valent pneumococcal polysaccharide vaccine; US, United States.

References:

  1. ABCs bact facts interactive data dashboard. SPN serotypes 1998-2023. Centers for Disease Control and Prevention. August 21, 2025. Accessed August 27, 2025. https://www.cdc.gov/abcs/bact-facts/data-dashboard.html
  2. 1998-2023 serotype data for invasive pneumococcal disease cases by age group from Active Bacterial Core surveillance. Centers for Disease Control and Prevention. Updated November 14, 2025. Accessed November 20, 2025. https://data.cdc.gov/Public-Health-Surveillance/1998-2023-Serotype-Data-for-Invasive-Pneumococcal-/qvzb-qs6p/about_data
  3. Kobayashi M, Leidner AJ, Gierke R, et al. Expanded recommendations for use of pneumococcal conjugate vaccines among adults aged ≥50 years: recommendations of the Advisory Committee on Immunization Practices — United States, 2024. MMWR Morb Mortal Wkly Rep. 2025;74(1):1-8. doi:10.15585/mmwr.mm7401a1
  4. Data available on request from Merck National Service Center via email at daprequests@merck.com. Please specify information package US-PVV-01008.
  5. Active Bacterial Core surveillance (ABCs) report, Emerging Infections Program network, Streptococcus pneumoniae, 2019. Centers for Disease Control and Prevention. Updated June 16, 2021. Accessed August 1, 2025. https://www.cdc.gov/abcs/downloads/SPN_Surveillance_Report_2019.pdf
  6. Active Bacterial Core surveillance (ABCs) report, Emerging Infections Program network, Streptococcus pneumoniae, 2020. Centers for Disease Control and Prevention. Updated September 20, 2022. Accessed August 1, 2025. https://stacks.cdc.gov/view/cdc/140328
  7. Active Bacterial Core surveillance (ABCs) report, Emerging Infections Program network, Streptococcus pneumoniae, 2021. Centers for Disease Control and Prevention. Updated June 2, 2023. Accessed August 4, 2025. https://www.cdc.gov/abcs/downloads/SPN_Surveillance_Report_2021.pdf
  8. Active Bacterial Core surveillance (ABCs) report, Emerging Infections Program network, Streptococcus pneumoniae, 2022. Centers for Disease Control and Prevention. Updated July 5, 2024. Accessed August 1, 2025. https://www.cdc.gov/abcs/downloads/SPN_Surveillance_Report_2022.pdf
  9. Active Bacterial Core surveillance (ABCs) report, Emerging Infections Program network, Streptococcus pneumoniae, 2023. Centers for Disease Control and Prevention. Updated March 20, 2025. Accessed July 28, 2025. https://www.cdc.gov/abcs/downloads/SPN_Surveillance_Report_2023.pdf
  10. Prevnar 20. Prescribing Information. Pfizer Inc; 2023.
patientSite

Indications

CAPVAXIVE® (Pneumococcal 21-valent Conjugate Vaccine) is indicated for:

  • active immunization for the prevention of invasive disease caused by Streptococcus pneumoniae serotypes 3, 6A, 7F, 8, 9N, 10A, 11A, 12F, 15A, 15B, 15C, 16F, 17F, 19A, 20A, 22F, 23A, 23B, 24F, 31, 33F, and 35B in individuals 18 years of age and older.
  • active immunization for the prevention of pneumonia caused by S. pneumoniae serotypes 3, 6A, 7F, 8, 9N, 10A, 11A, 12F, 15A, 15C, 16F, 17F, 19A, 20A, 22F, 23A, 23B, 24F, 31, 33F, and 35B in individuals 18 years of age and older.

The indication for the prevention of pneumonia caused by S. pneumoniae serotypes 3, 6A, 7F, 8, 9N, 10A, 11A, 12F, 15A, 15C, 16F, 17F, 19A, 20A, 22F, 23A, 23B, 24F, 31, 33F, and 35B is approved under accelerated approval based on immune responses as measured by opsonophagocytic activity (OPA). Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial.

Select Safety Information

Do not administer CAPVAXIVE® (Pneumococcal 21-valent Conjugate Vaccine) to individuals with a history of a severe allergic reaction (eg, anaphylaxis) to any component of CAPVAXIVE or to diphtheria toxoid.
 
Individuals with altered immunocompetence, including those receiving immunosuppressive therapy, may have a reduced immune response to CAPVAXIVE.
 
The most commonly reported (>10%) solicited adverse reactions in individuals 18 through 49 years of age who received CAPVAXIVE were: injection-site pain (73.1%), fatigue (36.0%), headache (27.5%), myalgia (16.4%), injection-site erythema (13.8%), and injection-site swelling (13.3%).
 
The most commonly reported (>10%) solicited adverse reactions in individuals 50 years of age and older who received CAPVAXIVE were: injection-site pain (41.2%), fatigue (19.7%), and headache (11.0%).
 
Vaccination with CAPVAXIVE may not protect all vaccine recipients.
 
Before administering CAPVAXIVE, please read the accompanying Prescribing Information. The Patient Information also is available.

Indications
Select Safety Information

CAPVAXIVE® (Pneumococcal 21-valent Conjugate Vaccine) is indicated for:

  • active immunization for the prevention of invasive disease caused by Streptococcus pneumoniae serotypes 3, 6A, 7F, 8, 9N, 10A, 11A, 12F, 15A, 15B, 15C, 16F, 17F, 19A, 20A, 22F, 23A, 23B, 24F, 31, 33F, and 35B in individuals 18 years of age and older.
  • active immunization for the prevention of pneumonia caused by S. pneumoniae serotypes 3, 6A, 7F, 8, 9N, 10A, 11A, 12F, 15A, 15C, 16F, 17F, 19A, 20A, 22F, 23A, 23B, 24F, 31, 33F, and 35B in individuals 18 years of age and older.

The indication for the prevention of pneumonia caused by S. pneumoniae serotypes 3, 6A, 7F, 8, 9N, 10A, 11A, 12F, 15A, 15C, 16F, 17F, 19A, 20A, 22F, 23A, 23B, 24F, 31, 33F, and 35B is approved under accelerated approval based on immune responses as measured by opsonophagocytic activity (OPA). Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial.

Select Safety Information

Do not administer CAPVAXIVE® (Pneumococcal 21-valent Conjugate Vaccine) to individuals with a history of a severe allergic reaction (eg, anaphylaxis) to any component of CAPVAXIVE or to diphtheria toxoid.
 
Individuals with altered immunocompetence, including those receiving immunosuppressive therapy, may have a reduced immune response to CAPVAXIVE.
 
The most commonly reported (>10%) solicited adverse reactions in individuals 18 through 49 years of age who received CAPVAXIVE were: injection-site pain (73.1%), fatigue (36.0%), headache (27.5%), myalgia (16.4%), injection-site erythema (13.8%), and injection-site swelling (13.3%).
 
The most commonly reported (>10%) solicited adverse reactions in individuals 50 years of age and older who received CAPVAXIVE were: injection-site pain (41.2%), fatigue (19.7%), and headache (11.0%).
 
Vaccination with CAPVAXIVE may not protect all vaccine recipients.
 
Before administering CAPVAXIVE, please read the accompanying Prescribing Information. The Patient Information also is available.