Dublin, April 09, 2021 (GLOBE NEWSWIRE) -- The "Disease Analysis: Pneumococcal Vaccines" report has been added to ResearchAndMarkets.com's offering.
The value of the pneumococcal vaccines market will steadily grow over the forecast period due to increasing elderly populations across France, Spain, and the US, alongside continued short-term price increases in the lucrative US market.
A brief period of increased growth is expected with the anticipated launch of the 20-valent vaccine, PF-06482077, which may replace Prevnar 13 and Pneumovax 23 in adults (from June 2021) and Prevnar 13/V114 in infants (from mid-2023). Overall, the biggest opportunity for short-term growth within the pneumococcal vaccines market is associated with increasing vaccination rates within the elderly in the US and Italian markets; however, the 2019 reversal of the original 2014 ACIP recommendation for Prevnar 13's use in the elderly population will hamper its growth in the US.
As the only vaccine routinely recommended for use in infants in the US, Japan, and five major European markets (France, Germany, Italy, Spain, and the UK), Prevnar 13 generates blockbuster revenues from this segment on account of large annual birth cohorts, high vaccination coverage rates, and its multi-dose schedule (2-4 doses are recommended depending on the market). However, Prevnar 13's high price point has resulted in very limited uptake in the elderly outside of the US, as the more affordable Pneumovax 23 is generally recommended for the elderly population, with the exception of Italy, where both vaccines are recommended.
The changing epidemiology of pneumococcal disease has influenced vaccine and dosing recommendations in the US and UK. In 2019, the US ACIP updated its vaccination guidance to remove its previous 2014 recommendation for the routine administration of a single dose of Prevnar 13 for all adults aged 65 years.
This change in stance was because the use of Prevnar 13 has caused a decline in invasive pneumococcal disease (IPD) incidence among adults and children (due to both direct and indirect herd protection effects), thus reducing the socioeconomic rationale for the vaccine's routine use in the elderly. Indeed, since the initial 2014 recommendation for Prevnar 13's use in the elderly, the incidence of IPD in the elderly has remained unchanged at five per 100,000 individuals, implying no clear population benefit of the previous recommendation.
From June 2021, Prevnar 13's market share in adults is expected to be cannibalized by Pfizer's 20-valent successor vaccine, PF-06482077, which could potentially void the need for separate Prevnar 13 and Pneumovax 23 vaccinations. In a Phase III study, the 20-valent vaccine has demonstrated non-inferiority to the 13 strains shared with Prevnar 13, in addition to non-inferior immunogenicity for six out of the seven shared strains with Pneumovax 23, with one serotype (8) narrowly missing non-inferiority criteria.
In addition, Prevnar 13 will also face competition in the infant segment for the first time from Merck & Co's 15-valent V114, which has broader serotype coverage and is expected to gain approval in the pediatric setting in H1 2022 (approval in adults is expected in July 2021, but PF-06482077 is expected to be preferred due to broader serotype coverage). To protect the company's market share in this lucrative segment, Pfizer is also investigating PF-06482077 in infants, and the publisher expects US and EU indication expansions to be granted in mid-2023.
As a pneumococcal polysaccharide vaccine, Pneumovax 23 is not recommended for routine use in infants as it does not stimulate protective immunity in this age range, which is thought to be due to the inability of individuals aged < 24 months to mount T-cell-independent humoral responses. The lack of an independent humoral response has resulted in Pneumovax 23's use being limited to the elderly, where its broad serotype coverage is attractive.
Pneumovax 23 sales are expected to grow through to Q3 2021 due to the increasing elderly population in France, Spain, and the US. However, following PF-06482077's anticipated approval from June 2021, Pneumovax 23's sales could plummet if PF-06482077 gains recommendations for preferential use from national immunization advisory groups.
Presently, there are six vaccines in clinical development within the US, Japan, and five major European markets, with Merck & Co's 15-valent V114 and Pfizer's 20-valent PF-06482077 both currently under regulatory review by the FDA for the prevention of pneumococcal disease in adults. Both vaccines possess broader serotype coverage than the currently recommended Prevnar 13 and hope to benefit commercially from serotype shift in pneumococcal disease incidence.
The overall likelihood of approval of a Phase I pneumococcal vaccine is 16.7%, and the average probability a vaccine advances from Phase III is 75%. Pneumococcal vaccines, on average, take 8.6 years from Phase I to approval, compared to 9.0 years in the overall infectious disease space.
Key Topics Covered:
OVERVIEW
- Latest key takeaways
DISEASE BACKGROUND
- Definition
- Symptoms
- Diagnosis
- Risk factors
VACCINATION GUIDELINES
- Vaccination guidelines in major markets
MARKETED VACCINES
PIPELINE VACCINES
KEY REGULATORY EVENTS
- Rejection Rate Soars In Q4 For EU Fast-Track Requests
- Pfizer Submits 20-Valent Successor To Prevnar 13
PROBABILITY OF SUCCESS
LICENSING AND ASSET ACQUISITION DEALS
- Shionogi Acquires Global Rights To HanaVax's Nasal Pneumococcal Vaccine
CLINICAL TRIAL LANDSCAPE
- Sponsors by status
- Sponsors by phase
- Recent events
VACCINE ASSESSMENT
- Prevnar 13
- Pneumovax 23
- V114
- PF-06482077
- Phase II vaccines to watch
MARKET DYNAMICS
FUTURE TRENDS
CONSENSUS FORECASTS
RECENT EVENTS AND ANALYST OPINION
- V114 for Pneumococcal Vaccines (September 9, 2020)
- V114 for Pneumococcal Vaccines (June 22, 2020)
- PF-06482077 for Pneumococcal Vaccines (March 18, 2020)
KEY UPCOMING EVENTS
KEY OPINION LEADER INSIGHTS
UNMET NEEDS
- Vaccines with broader serotype coverage to counter the threat of serotype shift
- Low coverage in miscellaneous "at-risk" groups
BIBLIOGRAPHY
- Prescription information
APPENDIX
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