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Safety and Immunogenicity of an Inactivated Recombinant Newcastle Disease Virus Vaccine Expressing SARS-CoV-2 Spike: Interim Results of a Randomised, Placebo-Controlled, Phase 1/2 Trial

Authors :
Punnee Pitisuttithum
Viravarn Luvira
Saranath Lawpoolsri
Sant Muangnoicharoen
Supitcha Kamolratanakul
Chaisith Sivakorn
Piengthong Narakorn
Somchaiya Surichan
Sumalee Prangpratanporn
Suttida Puksuriwong
Steven Lamola
Laina D. Mercer
Rama Raghunandan
Weina Sun
Yonghong Liu
Juan Manuel Carreño
Rami Scharf
Weerapong Phumratanaprapin
Fatima Amanat
Luc Gagnon
Ching-Lin Hsieh
Ruangchai Kaweepornpoj
Sarwat Khan
Manjari Lal
Stephen McCroskery
Jason McLellan
Ignacio Mena
Marcia Meseck
Benjaluck Phonrat
Yupa Sabmee
Ratsamikorn Singchareon
Stefan Slamanig
Nava Suthepakul
Johnstone Tcheou
Narumon Thantamnu
Sompone Theerasurakarn
Steven Tran
Thanakrit Vilasmongkolchai
Jessica A White
Nina Bhardwaj
Adolfo Garcia-Sastre
Peter Palese
Florian Krammer
Kittisak Poopipatpol
Ponthip Wirachwong
Richard Hjorth
Bruce L Innis
Source :
medRxiv
Publication Year :
2021
Publisher :
Cold Spring Harbor Laboratory, 2021.

Abstract

SummaryBackgroundProduction of affordable coronavirus disease 2019 (COVID-19) vaccines in low- and middle-income countries is needed. NDV-HXP-S is an inactivated egg-based Newcastle disease virus vaccine expressing the spike protein of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). It’s being developed in Thailand, Vietnam, and Brazil; herein are initial results from Thailand.MethodsThis phase 1 stage of a randomised, dose-escalation, observer-blind, placebo-controlled, phase 1/2 trial was conducted at the Vaccine Trial Centre, Mahidol University (Bangkok). Healthy adults aged 18-59 years, non-pregnant and negative for SARS-CoV-2 antibodies were eligible. Participants were block randomised to receive one of six treatments by intramuscular injection twice, 28 days apart: 1 µg±CpG1018 (a toll-like receptor 9 agonist), 3 µg±CpG1018, 10 µg, or placebo. Participants and personnel assessing outcomes were masked to treatment. The primary outcomes were solicited and spontaneously reported adverse events (AEs) during 7 and 28 days after each vaccination, respectively. Secondary outcomes were immunogenicity measures (anti-S IgG and pseudotyped virus neutralisation). An interim analysis assessed safety at day 57 in treatment-exposed individuals and immunogenicity through day 43 per protocol. ClinicalTrials.gov (NCT04764422).FindingsBetween March 20 and April 23, 2021, 377 individuals were screened and 210 were enrolled (35 per group); all received dose one; five missed dose two. The most common solicited AEs among vaccinees, all predominantly mild, were injection site pain (InterpretationNDV-HXP-S had an acceptable safety profile and potent immunogenicity. The 3 µg and 3 µg+CpG1018 formulations advanced to phase 2.FundingNational Vaccine Institute (Thailand), National Research Council (Thailand), Bill & Melinda Gates Foundation, National Institutes of Health (USA)

Details

Database :
OpenAIRE
Journal :
medRxiv
Accession number :
edsair.doi.dedup.....20ff513b3ce313d4926c1fba4605cb46
Full Text :
https://doi.org/10.1101/2021.09.17.21263758