Publication of clinical trial results
The information given below and the relevant links to the clinical data fulfil the requirements of Articles 71-73 of the Ordinance on Therapeutic Products (Therapeutic Products Ordinance, TPO). They supplement the information published in association with the Swiss marketing authorisation for the medicinal product.
VAXNEUVANCE®
Pneumococcal polysaccharide conjugate vaccine (15 valent, adsorbed). Suspension for injection.
1 dose (0.5 ml) contains:
- Pneumococcal polysaccharide serotype 11,2 2.0 micrograms
- Pneumococcal polysaccharide serotype 31,2 2.0 micrograms
- Pneumococcal polysaccharide serotype 41,2 2.0 micrograms
- Pneumococcal polysaccharide serotype 51,2 2.0 micrograms
- Pneumococcal polysaccharide serotype 6A1,2 2.0 micrograms
- Pneumococcal polysaccharide serotype 6B1,2 4.0 micrograms
- Pneumococcal polysaccharide serotype 7F1,2 2.0 micrograms
- Pneumococcal polysaccharide serotype 9V1,2 2.0 micrograms
- Pneumococcal polysaccharide serotype 141,2 2.0 micrograms
- Pneumococcal polysaccharide serotype 18C1,2 2.0 micrograms
- Pneumococcal polysaccharide serotype 19A1,2 2.0 micrograms
- Pneumococcal polysaccharide serotype 19F1,2 2.0 micrograms
- Pneumococcal polysaccharide serotype 22F1,2 2.0 micrograms
- Pneumococcal polysaccharide serotype 23F1,2 2.0 micrograms
- Pneumococcal polysaccharide serotype 33F 1,22.0 micrograms
1 Conjugated to CRM197 carrier protein. CRM197 is a non-toxic mutant of diphtheria toxin (from Corynebacterium diphtheriae C7) and was recombinantly expressed in Pseudomonas fluorescens.
2 Adsorbed to aluminum phosphate adjuvant.
1 dose (0.5 ml) contains 125 micrograms of aluminum (Al3+) and approximately 30 micrograms of CRM197 carrier protein.
Authorisation number: 68752
Date of Marketing Authorisation: 14-Feb-2023
Clinical Trials
Safety and Immunogenicity of V114 in Healthy Adults (V114-019/PNEU-AGE) – ClinicalTrials.gov
NCT03950622
Publication:
Platt HL, Cardona JF, Haranaka M, Schwartz HI, Narejos Perez S, Dowell A, Chang CJ, Dagan R, Tamms GM, Sterling T, Morgan L, Shi Y, Pedley A, Musey LK, Buchwald UK. A phase 3 trial of safety, tolerability, and immunogenicity of V114, 15-valent pneumococcal conjugate vaccine, compared with 13-valent pneumococcal conjugate vaccine in adults 50 years of age and older (PNEU-AGE). Vaccine. 2022 Jan 3;40(1):162-172. doi: 10.1016/j.vaccine.2021.08.049. Epub 2021 Sep 8. PMID: 34507861.
Publication:
Song JY, Chang CJ, Andrews C, Diez-Domingo J, Oh MD, Dagan R, Hartzel J, Pedley A, Li J, Sterling T, Tamms G, Chiarappa JA, Lutkiewicz J, Musey L, Tu Y, Buchwald UK; V114-016 (PNEU-PATH) study group. Safety, tolerability, and immunogenicity of V114, a 15-valent pneumococcal conjugate vaccine, followed by sequential PPSV23 vaccination in healthy adults aged ≥50 years: A randomized phase III trial (PNEU-PATH). Vaccine. 2021 Oct 15;39(43):6422-6436. doi: 10.1016/j.vaccine.2021.08.038. Epub 2021 Sep 4. PMID: 34489128.
Publication:
Peterson JT, Stacey HL, MacNair JE, Li J, Hartzel JS, Sterling TM, Benner P, Tamms GM, Musey LK. Safety and immunogenicity of 15-valent pneumococcal conjugate vaccine compared to 13-valent pneumococcal conjugate vaccine in adults ≥65 years of age previously vaccinated with 23-valent pneumococcal polysaccharide vaccine. Hum Vaccin Immunother. 2019;15(3):540-548. doi: 10.1080/21645515.2018.1532250. Epub 2018 Nov 14. PMID: 30427749; PMCID: PMC6605723.
Publication:
Severance R, Schwartz H, Dagan R, Connor L, Li J, Pedley A, Hartzel J, Sterling TM, Nolan KM, Tamms GM, Musey LK, Buchwald UK. Safety, tolerability, and immunogenicity of V114, a 15-valent pneumococcal conjugate vaccine, administered concomitantly with influenza vaccine in healthy adults aged ≥50 years: a randomized phase 3 trial (PNEU-FLU). Hum Vaccin Immunother. 2022 Dec 31;18(1):1-14. doi: 10.1080/21645515.2021.1976581. Epub 2021 Nov 2. PMID: 34726574; PMCID: PMC8920144.
CH-PVC-00033, 05/2023