A Phase 1/2a Study Evaluating Safety and Immunogenicity of Ad26.RSV.preF in RSV-seronegative Toddlers Aged 12–24 Months

Author:

Langley Joanne M1,Nolan Terry M23,Rämet Mika4,Richmond Peter C56,Rosário Filho Nelson7,Haazen Wouter8,van den Berg Sara P H8,Williams Kristi8,Bastian Arangassery Rosemary8,Omoruyi Edmund9,Williams Durkin Joanna10,Salisch Nadine8,Van Geet Gunter11,van Duijnhoven Wilbert11,Heijnen Esther8,Callendret Benoit8

Affiliation:

1. Canadian Center for Vaccinology, Dalhousie University, IWK and Nova Scotia Health , Halifax, Nova Scotia , Canada

2. Department of Infectious Diseases, Peter Doherty Institute for Infection and Immunity at The University of Melbourne , Melbourne, Victoria , Australia

3. Murdoch Children's Research Institute , Melbourne, Victoria , Australia

4. FVR – Finnish Vaccine Research Ltd., and Faculty of Medicine and Health Technology, Tampere University , Tampere , Finland

5. Wesfarmers Centre of Vaccines and Infectious Diseases, Telethon Kids Institute, University of Western Australia , Perth, Western Australia , Australia

6. Discipline of Paediatrics, School of Medicine, University of Western Australia , Perth, Western Australia , Australia

7. Division of Allergy and Immunology, Complexo Hospital de Clínicas da Universidade Federal do Paraná , Curitiba , Brazil

8. Janssen Vaccines & Prevention B.V. , Leiden , The Netherlands

9. Janssen Infectious Diseases , Beerse , Belgium

10. Janssen Biologics Europe , Leiden , The Netherlands

11. Janssen Research & Development , Beerse , Belgium

Abstract

Abstract Background Respiratory syncytial virus (RSV) causes serious illness in children. The Ad26.RSV.preF vaccine candidate was immunogenic with acceptable safety in a phase 1/2a study of RSV-seropositive children. Here, we assessed its safety and immunogenicity in RSV-seronegative children. Methods In this randomized, observer-blinded, placebo-controlled, phase 1/2a study (NCT03606512; https://www.clinicaltrials.gov/ct2/show/NCT03606512), RSV-seronegative toddlers aged 12–24 months received Ad26.RSV.preF (2.5 × 1010 viral particles) or placebo on days 1, 29, and 57 (a meningococcal vaccine [Nimenrix] could substitute for day 57 placebo). Primary endpoints were solicited local and systemic adverse events (AEs; 7 days after each vaccination), unsolicited AEs (28 days postvaccination), and serious AEs (first vaccination until study end). Participants were monitored for RSV-respiratory tract infection to assess infection rates and for severe RSV-lower respiratory tract infection as an indication of enhanced disease. RSV-A2 neutralizing, RSV (A and B) preF binding, and RSV postF immunoglobulin G–binding antibodies were evaluated on days 1 (predose), 8, and 85, and after RSV season 1. Results Thirty-eight participants were enrolled and vaccinated (Ad26.RSV.preF, n = 20; placebo, placebo/Nimenrix, n = 18). Solicited AEs were more common following Ad26.RSV.preF than placebo; most were mild/moderate. No vaccine-related serious AEs were reported. Five of 19 participants receiving Ad26.RSV.preF and 2/18 receiving placebo or placebo/Nimenrix had confirmed RSV-respiratory tract infection or RSV-associated otitis media; none were considered severe. At the final season 1 study visit, most Ad26.RSV.preF recipients had ≥2-fold increases from baseline in RSV-A2 neutralizing, RSV A and B preF binding, and RSV postF antibodies. Conclusions Ad26.RSV.preF was well tolerated and immunogenic in RSV-seronegative toddlers.

Funder

Janssen Vaccines & Prevention B.V.

Publisher

Oxford University Press (OUP)

Reference31 articles.

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