STRIDE-8 (NCT05696080) is a phase 3, double-blind, randomised (3:1) trial comparing V116 with PCV15 (administered Day 1) followed by PPSV23 (administered Week 8). Dr Heather Platt (Merck & Co., Inc., NJ, USA) presented the results [1]. Participants were adults aged 18-64 years with underlying chronic medical conditions and no prior pneumococcal vaccination. Outcomes included immunogenicity (opsonophagocytic activity (OPA) mean geometric titres (GMT) at Day 30 for V116 and at Week 12 for PCV15 plus PPSV23), as well as safety. Overall, 516 adults were enrolled: 386 received V116 and 130 PCV15 on Day 1.
V116 demonstrated immunogenicity against all 21 serotypes included in the vaccine. OPA GMTs showed comparable responses to the PCV15 plus PPSV23 for common serotypes (3, 6A, 7F, 8, 9N, 10A, 11A, 12F, 17F, 19A, 20A, 22F, 33F) and higher responses for the serotypes unique to V116 (15A, 15C, 16F, 23A, 23B, 24F, 31, 35B). The safety profile of V116 was favourable, with lower rates of overall adverse events compared with PCV15 plus PPSV23 (68.7% vs 90.8%), including fewer local reactions (such as injection-site pain, erythema, and swelling) and systemic reactions.
The authors concluded that V116 had a favourable safety profile versus PCV15 plus PPSV23 in vaccine-naïve participants aged 18-64 years with underlying chronic medical conditions. Immunogenicity was confirmed for all 21 serotypes, showing comparable protection against shared serotypes and enhanced responses for the 8 unique serotypes.
- Scott P, et al. A phase 3, randomised trial investigating the safety, tolerability, and immunogenicity of V116, an adult-specific pneumococcal conjugate vaccine, in adults with increased risk for pneumococcal disease (STRIDE-8). 6th ESCMID Conference on Vaccines, 10–13 September 2025, Lisbon, Portugal.
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Table of Contents: ESCMID Vaccines 2025
Featured articles
Real-world data confirm PCV20 effectiveness against pneumococcal disease in adults aged ≥65 years
Pneumococcal Vaccination
A quarter of US children have incomplete pneumococcal vaccination by age 2
V116 shows promise for adults at risk of pneumococcal disease
Real-world data confirm PCV20 effectiveness against pneumococcal disease in adults aged ≥65 years
The V116 pneumococcal vaccine is a new option in children at risk for pneumococcal disease
Influenza and COVID-19 Vaccination
Omicron XBB.1.5 vaccination provides effective, but rapidly waning protection in immunocompromised individuals
Intranasal COVID-19 vaccine shows promising results in preclinical mouse models
Influenza vaccine in children shows moderate, broad protection during the 2024-2025 season
Lower age is linked to reduced uptake of influenza and COVID-19 vaccination
RSV vaccination and Immunisation
Combination respiratory vaccines show promise but face key challenges
Adjuvanted RSVPreF3 demonstrates high real-world effectiveness in the USA
RSV immunisation: Maternal versus direct infant immunisation
European pregnant women show openness to maternal RSV vaccination
Infants immunised with nirsevimab have a lower risk of respiratory-related recurrent hospitalisation
Adjuvanted RSVPreF3 can be co-administered with a COVID-19 mRNA vaccine in adults aged ≥50 years
Other Childhood and Routine Vaccinations
Pertussis vaccination: Could an intranasal vaccine help curb the rising cases of whooping cough?
Does the 2+1 vaccination schedule for Haemophilus influenzae type b increase case numbers?
Wastewater poliovirus detections in Europe may reflect seasonal infection patterns rather than consistent importation
Emerging and Future Vaccines
Where do we stand with vaccination for haemolytic streptococci?
The future looks promising for tuberculosis vaccination
Where do alternative vaccine administration routes fit in the clinical landscape?
Malaria immunisation beyond subunit vaccines: Current progress
SARI Definitions and Vaccine Effectiveness
Case definition discrepancies influence VE outcomes
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