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

Langley, Joanne M.; Nolan, Terry M.; Rämet, Mika; Richmond, Peter C.; Filho, Nelson Rosário; Haazen, Wouter; van den Berg, Sara P.H.; Williams, Kristi; Bastian, Arangassery Rosemary; Omoruyi, Edmund; Durkin, Joanna Williams; Salisch, Nadine; Van Geet, Gunter; van Duijnhoven, Wilbert; Heijnen, Esther; Callendret, Benoit (2024)

 
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Langley, Joanne M.
Nolan, Terry M.
Rämet, Mika
Richmond, Peter C.
Filho, Nelson Rosário
Haazen, Wouter
van den Berg, Sara P.H.
Williams, Kristi
Bastian, Arangassery Rosemary
Omoruyi, Edmund
Durkin, Joanna Williams
Salisch, Nadine
Van Geet, Gunter
van Duijnhoven, Wilbert
Heijnen, Esther
Callendret, Benoit
2024

Open Forum Infectious Diseases
ofae453
doi:10.1093/ofid/ofae453
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Julkaisun pysyvä osoite on
https://urn.fi/URN:NBN:fi:tuni-202410229424

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Peer reviewed
Tiivistelmä
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.
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Kalevantie 5
PL 617
33014 Tampereen yliopisto
oa[@]tuni.fi | Tietosuoja | Saavutettavuusseloste