An Investigator Initiated, Randomized, Double-blinded, Placebo-controlled Clinical Trial to Evaluate the Safety, Immunogenicity and Efficacy of the Recombinant Two-component COVID-19 Vaccine (CHO Cell) in Adults Aged 18 Years and Older

Study Background Currently, the continued prevalence and mutation of SARS-CoV-2 variants has increased the urgency of optimizing the epidemic prevention strategy. Data from numerous studies show that booster vaccination with traditional COVID-19 vaccine can induce certain levels of antibodies and have a neutralizing effect on variants, which is the main means of responding to the current outbreak. By the end of November 2022, the booster vaccination rate of COVID-19 vaccine in China has exceeded 70%. However, recently, the surge in the number of infections and the strain on medical resources have made the task of the epidemic prevention increasingly difficult. The research and development of a new generation of COVID-19 vaccine with better broad-spectrum cross-neutralizing activity against endemic strains has become an important direction for the prevention of SARS-CoV-2 epidemics.

The recombinant two-component COVID-19 vaccine (CHO cell) developed and produced by Jiangsu Recbio Biotechnology Co., LTD. ( Recbio ), referred to as "ReCOV", is a new structurally designed COVID-19 vaccine guided by neutralizing antibodies. The antigen of ReCOV is selected from the amino acid sequence 14-541 (NTD and RBD structural domains) of Spike protein of SARS-CoV-2 prototype strain, and the foldon structural domain derived from T4 phage is fused at the C-terminus to form a trimerized protein containing NTD-RBD-foldon. For clinical use, a novel adjuvant BFA03 (similar to AS03 developed by GSK) consisting of squalene, α-tocopherol and polysorbate 80 is mixed to induce the body to produce specific neutralizing antibodies, block the binding of SARS-CoV-2 to the host, stimulate the body to produce anti-SARS-CoV-2 immunity, and is used to prevent the disease caused by SARS-CoV-2 infection. Non-clinical studies have shown that ReCOV was safe and well tolerated, with strong neutralizing effects against the prototype SARS-CoV-2 strain and multiple variants, and protection against SARS-CoV-2 attack.

To date, ReCOV's overseas clinical studies are actively underway. Among them, the phase I study of primary immunity has been completed, and three phase II studies of primary and sequential booster immunity will be completed in the near future for primary and interim analyses, respectively. The Phase III international multicenter study on the efficacy of primary immunity protection was initiated at the end of October 2022, and as of the preparation of this study protocol, more than 2,000 subjects have been enrolled and completed the first dose of vaccine, of which more than 1,000 have received two doses. During the same period, the ReCOV in-country Phase I study is ongoing. Phase I and II studies of ReCOV in both Caucasian and Asian populations showed good safety profiles, with no serious vaccine-related adverse events or adverse events leading to early study withdrawal reported, and the majority of adverse events were grade 1-2. Blinded data from the phase III study of primary immunization showed that the overall safety of ReCOV vaccination was good, and the safety characteristics were consistent with those of the phase I and II studies. The primary immunization study showed that two doses of ReCOV vaccination induced high levels of neutralizing antibodies against the prototype strain of the live virus and a significant Th1-biased cellular immune response with good immune persistence. Phase II studies of primary and sequential booster immunizations showed that ReCOV-induced neutralizing antibodies produced high levels of cross-neutralization against Omicron BA.2, BA.4/5, and BA.2.75 variants, with only 1.6 to 2.0-fold, 2.0 to 3.5-fold, and 2.6 to 3.0-fold decreases in titers compared to the prototype strain, respectively. Neutralizing antibody levels induced by the ReCOV sequential booster against the prototype strain and the Omicron BA.2, BA.4/5, and BA.2.75 variants were 10.8 to 17.3 times higher than the homologous booster of the control inactivated vaccine and significantly better than the heterologous booster immunization of the Pfizer mRNA vaccine.Data from all studies have shown that ReCOV is well tolerated and safe, with excellent immunogenicity and strong cross-protection against the current SARS-CoV-2 epidemic strain. Based on the previous clinical studies, this study will further evaluate the safety and immunogenicity of ReCOV booster immunization and explore its protective efficacy against SARS-CoV-2 infection and COVID-19 in Chinese population that has completed 2 or 3 doses of inactivated COVID-19 vaccine.

Study Design：This is a randomized, double-blind, placebo-controlled study to evaluate the safety, immunogenicity, and protective efficacy of a booster dose of ReCOV in a healthy Chinese population aged 18 years and older who have completed 2 or 3 doses of inactivated COVID-19 vaccine 6 to 18 months (180 to 540 days) after vaccination and who have been asked about their history of COVID-19 within the previous 6 months.Approximately 3300 participants will be enrolled, including an immunogenic subgroup of approximately 240. Approximately 10% to 15% of all subjects will be 60 years of age and older. Enrolled subjects will be stratified by age (18-59 years, 60 years and older), number of previous doses of COVID-19 vaccine (2 or 3 doses), and interval from the last previous dose (180-365 days, 366-540 days). Participants will be randomized in a 1:1 ratio to receive 1 dose of the ReCOV or placebo on Day 0.The study is divided into a screening period, a vaccination and follow-up period (randomization to 30 days after completion of booster immunization), and a long-term follow-up period (30 days after completion of booster immunization followed up to 6 months). At the end of the study vaccination and follow-up period, a first interim analysis (Interim Analysis, IA-1) of safety and available immunogenicity data will be performed. This will be followed by a 2nd interim analysis (Interim Analysis, IA-2) when at least 66.7% of the total number of target symptomatic COVID-19 endpoint cases have been collected (i.e., at least 103 symptomatic COVID-19 endpoint cases). Thereafter, a final analysis of safety, immunogenicity, and protective efficacy (Final Analysis, FA) will be performed after 6 months of follow-up after all subjects have completed booster immunization.

Safety observations All AEs within 30 minutes, solicited (local and systemic) AE within 7 days and unsolicited AE within 30 days after vaccination in all participants will be assessed. To assess the incidence, severity, and causality of SAEs and of AESI, and the occurrence of pregnancy events [newborns follow-up for at least 12 months after birth (female participant pregnancies and male participant partner pregnancies, mainly focus on newborn birth defects, abnormal growth and development, abnormal immune function and other events)], in all participants within 6 months after vaccination.