Safety and immunogenicity of an egg-based inactivated Newcastle disease virus vaccine expressing SARS-CoV-2 spike: Interim results of a randomized, placebo-controlled, phase 1/2 trial in Vietnam
Issued Date
2022-06-09
Resource Type
ISSN
0264410X
eISSN
18732518
Scopus ID
2-s2.0-85130342498
Pubmed ID
35577631
Journal Title
Vaccine
Volume
40
Issue
26
Start Page
3621
End Page
3632
Rights Holder(s)
SCOPUS
Bibliographic Citation
Vaccine Vol.40 No.26 (2022) , 3621-3632
Suggested Citation
Duc Dang A., Dinh Vu T., Hai Vu H., Thanh Ta V., Thi Van Pham A., Thi Ngoc Dang M., Van Le B., Huu Duong T., Van Nguyen D., Lawpoolsri S., Chinwangso P., McLellan J.S., Hsieh C.L., Garcia-Sastre A., Palese P., Sun W., Martinez J.L., Gonzalez-Dominguez I., Slamanig S., Manuel Carreño J., Tcheou J., Krammer F., Raskin A., Minh Vu H., Cong Tran T., Mai Nguyen H., Mercer L.D., Raghunandan R., Lal M., White J.A., Hjorth R., Innis B.L., Scharf R. Safety and immunogenicity of an egg-based inactivated Newcastle disease virus vaccine expressing SARS-CoV-2 spike: Interim results of a randomized, placebo-controlled, phase 1/2 trial in Vietnam. Vaccine Vol.40 No.26 (2022) , 3621-3632. 3632. doi:10.1016/j.vaccine.2022.04.078 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/83699
Title
Safety and immunogenicity of an egg-based inactivated Newcastle disease virus vaccine expressing SARS-CoV-2 spike: Interim results of a randomized, placebo-controlled, phase 1/2 trial in Vietnam
Author(s)
Duc Dang A.
Dinh Vu T.
Hai Vu H.
Thanh Ta V.
Thi Van Pham A.
Thi Ngoc Dang M.
Van Le B.
Huu Duong T.
Van Nguyen D.
Lawpoolsri S.
Chinwangso P.
McLellan J.S.
Hsieh C.L.
Garcia-Sastre A.
Palese P.
Sun W.
Martinez J.L.
Gonzalez-Dominguez I.
Slamanig S.
Manuel Carreño J.
Tcheou J.
Krammer F.
Raskin A.
Minh Vu H.
Cong Tran T.
Mai Nguyen H.
Mercer L.D.
Raghunandan R.
Lal M.
White J.A.
Hjorth R.
Innis B.L.
Scharf R.
Dinh Vu T.
Hai Vu H.
Thanh Ta V.
Thi Van Pham A.
Thi Ngoc Dang M.
Van Le B.
Huu Duong T.
Van Nguyen D.
Lawpoolsri S.
Chinwangso P.
McLellan J.S.
Hsieh C.L.
Garcia-Sastre A.
Palese P.
Sun W.
Martinez J.L.
Gonzalez-Dominguez I.
Slamanig S.
Manuel Carreño J.
Tcheou J.
Krammer F.
Raskin A.
Minh Vu H.
Cong Tran T.
Mai Nguyen H.
Mercer L.D.
Raghunandan R.
Lal M.
White J.A.
Hjorth R.
Innis B.L.
Scharf R.
Author's Affiliation
Other Contributor(s)
Abstract
Production 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 (NDV) vaccine expressing the spike protein of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Wuhan-Hu-1. The spike protein was stabilized and incorporated into NDV virions by removing the polybasic furin cleavage site, introducing the transmembrane domain and cytoplasmic tail of the fusion protein of NDV, and introducing six prolines for stabilization in the prefusion state. Vaccine production and clinical development was initiated in Vietnam, Thailand, and Brazil. Here the interim results from the first stage of the randomized, dose-escalation, observer-blind, placebo-controlled, phase 1/2 trial conducted at the Hanoi Medical University (Vietnam) are presented. Healthy adults aged 18–59 years, non-pregnant, and with self-reported negative history for SARS-CoV-2 infection were eligible. Participants were randomized to receive one of five treatments by intramuscular injection twice, 28 days apart: 1 μg +/- CpG1018 (a toll-like receptor 9 agonist), 3 μg alone, 10 μg alone, or placebo. Participants and personnel assessing outcomes were masked to treatment. The primary outcomes were solicited adverse events (AEs) during 7 days and subject-reported AEs during 28 days after each vaccination. Investigators further reviewed subject-reported AEs. Secondary outcomes were immunogenicity measures (anti-spike immunoglobulin G [IgG] and pseudotyped virus neutralization). This interim analysis assessed safety 56 days after first vaccination (day 57) in treatment-exposed individuals and immunogenicity through 14 days after second vaccination (day 43) per protocol. Between March 15 and April 23, 2021, 224 individuals were screened and 120 were enrolled (25 per group for active vaccination and 20 for placebo). All subjects received two doses. The most common solicited AEs among those receiving active vaccine or placebo were all predominantly mild and included injection site pain or tenderness (<58%), fatigue or malaise (<22%), headache (<21%), and myalgia (<14%). No higher proportion of the solicited AEs were observed for any group of active vaccine. The proportion reporting vaccine-related AEs during the 28 days after either vaccination ranged from 4% to 8% among vaccine groups and was 5% in controls. No vaccine-related serious adverse event occurred. The immune response in the 10 μg formulation group was highest, followed by 1 μg + CpG1018, 3 μg, and 1 μg formulations. Fourteen days after the second vaccination, the geometric mean concentrations (GMC) of 50% neutralizing antibody against the homologous Wuhan-Hu-1 pseudovirus ranged from 56.07 IU/mL (1 μg, 95% CI 37.01, 84.94) to 246.19 IU/mL (10 μg, 95% CI 151.97, 398.82), with 84% to 96% of vaccine groups attaining a ≥ 4-fold increase over baseline. This was compared to a panel of human convalescent sera (N = 29, 72.93 95% CI 33.00–161.14). Live virus neutralization to the B.1.617.2 (Delta) variant of concern was reduced but in line with observations for vaccines currently in use. Since the adjuvant has shown modest benefit, GMC ratio of 2.56 (95% CI, 1.4–4.6) for 1 μg +/- CpG1018, a decision was made not to continue studying it with this vaccine. NDV-HXP-S had an acceptable safety profile and potent immunogenicity. The 3 μg dose was advanced to phase 2 along with a 6 μg dose. The 10 μg dose was not selected for evaluation in phase 2 due to potential impact on manufacturing capacity. ClinicalTrials.gov NCT04830800.