Final efficacy analysis, interim safety analysis, and immunogenicity of a single dose of recombinant novel coronavirus vaccine (adenovirus type 5 vector) in adults 18 years and older: an international, multicentre, randomised, double-blinded, placebo-controlled phase 3 trial

Abstract

Background: The Ad5-nCoV vaccine is a single-dose adenovirus type 5 (Ad5) vectored vaccine expressing the SARS-CoV-2 spike protein that was well-tolerated and immunogenic in phase 1 and 2 studies. In this study, we report results on the final efficacy and interim safety analyses of the phase 3 trial.

Methods: This double-blind, randomised, international, placebo-controlled, endpoint-case driven, phase 3, clinical trial enrolled adults aged 18 years older at study centres in Argentina, Chile, Mexico, Pakistan, and Russia. Participants were eligible for the study if they had no unstable or severe underlying medical or psychiatric conditions; had no history of a laboratory-confirmed SARS-CoV-2 infection; were not pregnant or breastfeeding; and had no previous receipt of an adenovirus-vectored, coronavirus, or SARS-CoV-2 vaccine. After informed consent was obtained, 25 mL of whole blood was withdrawn from all eligible participants who were randomised in a 1:1 ratio to receive a single intramuscular dose of 0·5 mL placebo or a 0·5 mL dose of 5 × 1010 viral particle (vp)/mL Ad5-nCoV vaccine; study staff and participants were blinded to treatment allocation. All participants were contacted weekly by email, telephone, or text message to self-report any symptoms of COVID-19 illness, and laboratory testing for SARS-CoV-2 was done for all participants with any symptoms. The primary efficacy objective evaluated Ad5-nCoV in preventing symptomatic, PCR-confirmed COVID-19 infection occurring at least 28 days after vaccination in all participants who were at least 28 days postvaccination on Jan 15, 2021. The primary safety objective evaluated the incidence of any serious adverse events or medically attended adverse events postvaccination in all participants who received a study injection. This trial is closed for enrolment and is registered with ClinicalTrials.gov (NCT04526990).

Findings: Study enrolment began on Sept 22, 2020, in Pakistan, Nov 6, 2020, in Mexico, Dec 2, 2020, in Russia and Chile, and Dec 17, 2020, in Argentina; 150 endpoint cases were reached on Jan 15, 2021, triggering the final primary efficacy analysis. One dose of Ad5-nCoV showed a 57·5% (95% CI 39·7-70·0, p=0·0026) efficacy against symptomatic, PCR-confirmed, COVID-19 infection at 28 days or more postvaccination (21 250 participants; 45 days median duration of follow-up [IQR 36-58]). In the primary safety analysis undertaken at the time of the efficacy analysis (36 717 participants), there was no significant difference in the incidence of serious adverse events (14 [0·1%] of 18 363 Ad5-nCoV recipients and 10 [0·1%] of 18 354 placebo recipients, p=0·54) or medically attended adverse events (442 [2·4%] of 18 363 Ad5-nCoV recipients and 411 [2·2%] of 18 354 placebo recipients, p=0·30) between the Ad5-nCoV or placebo groups, or any serious adverse events considered related to the study product (none in both Ad5-nCoV and placebo recipients). In the extended safety cohort, 1004 (63·5%) of 1582 of Ad5-nCoV recipients and 729 (46·4%) of 1572 placebo recipients reported a solicited systemic adverse event (p<0·0001), of which headache was the most common (699 [44%] of Ad5-nCoV recipients and 481 [30·6%] of placebo recipients; p<0·0001). 971 (61·3%) of 1584 Ad5-nCoV recipients and 314 (20·0%) of 1573 placebo recipients reported an injection-site adverse event (p<0·0001), of which pain at the injection site was the most frequent; reported by 939 (59%) Ad5-nCoV recipients and 303 (19%) placebo recipients.

Interpretation: One dose of Ad5-nCoV is efficacious and safe in healthy adults aged 18 years and older.

Funding: CanSino Biologics and the Beijing Institute of Biotechnology.

Conflict of interest statement

Declaration of interests JG and TZ are employees of and own stock in CanSino Biologics, and LB is a senior scientific advisor to CanSino Biologics. All other authors received funding to their institutions to perform the clinical trial but did not receive any personal funding.

Copyright © 2022 Elsevier Ltd. All rights reserved.

Figures

Figure 1

Clinical trial profile Disposition of clinical trial participants for the efficacy analysis and safety analysis at the cutoff date of the efficacy analysis (Jan 15, 2021; A), and the extended safety and immunogenicity analyses at the cut off date for the extended safety and immunogenicity analyses (March 15, 2021; B). A subset (n=538) of participants in the extended safety and immunogenicity analyses were in the immunogenicity subcohort, allocated randomly to placebo (n=267) or Ad5-nCoV (n=271). All were included in the immunogenicity analysis. The extended immunogenicity results will be presented at a later date. *Second study identification number for double vaccinated participants are individuals who, unknown to study staff, enrolled in the study twice and were randomly assigned twice and received two study injections. In the intention-to-treat analysis, they were analysed according to the first randomisation allocation. †The unknown vaccine arose because two participants were randomised with the same dispensing code, and it is unclear which vaccine they received.

Figure 1

Clinical trial profile Disposition of clinical trial participants for the efficacy analysis and safety analysis at the cutoff date of the efficacy analysis (Jan 15, 2021; A), and the extended safety and immunogenicity analyses at the cut off date for the extended safety and immunogenicity analyses (March 15, 2021; B). A subset (n=538) of participants in the extended safety and immunogenicity analyses were in the immunogenicity subcohort, allocated randomly to placebo (n=267) or Ad5-nCoV (n=271). All were included in the immunogenicity analysis. The extended immunogenicity results will be presented at a later date. *Second study identification number for double vaccinated participants are individuals who, unknown to study staff, enrolled in the study twice and were randomly assigned twice and received two study injections. In the intention-to-treat analysis, they were analysed according to the first randomisation allocation. †The unknown vaccine arose because two participants were randomised with the same dispensing code, and it is unclear which vaccine they received.

Figure 2

Cumulative incidence of COVID-19 with onset at least 1-day postvaccination with either Ad5-nCoV or placebo Cases were all PCR-confirmed cases, adjudicated by the independent endpoint review committee. Ad5-nCoV=adenovirus type 5 (Ad5) vectored vaccine expressing the SARS-CoV-2 spike protein.