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Safety and Immunogenicity of an Inactivated COVID-19 Vaccine, WIBP-CorV, in Healthy Children: Interim Analysis of a
Shengli Xia1, Kai Duan2, Yuntao Zhang3
1Vaccine Clinical Research Center, Henan Center for Disease Control and Prevention, Zhengzhou, China.
Insights
This study found the inactivated COVID-19 vaccine WIBP-CorV to be safe and effective in children aged 3-17 years. It generated robust antibody responses lasting at least six months, with mild side effects.
Area of Science:
- Vaccinology
- Pediatric Infectious Diseases
- Immunology
Background:
- Urgent need for safe and effective SARS-CoV-2 vaccines for pediatric populations.
- WIBP-CorV is an inactivated COVID-19 vaccine candidate.
Purpose of the Study:
- To assess the safety and immunogenicity of WIBP-CorV in children aged 3-17 years.
- Evaluate immune responses and adverse events following vaccination.
Main Methods:
- Phase 1/2, randomized, double-blind, placebo-controlled clinical trial in China.
- 240 participants (Phase 1) and 576 participants (Phase 2) aged 3-17 years.
- Three intramuscular injections of WIBP-CorV (2.5, 5.0, or 10.0μg/dose) or placebo at 0, 28, and 56 days.
Main Results:
- WIBP-CorV demonstrated a favorable safety profile with mild, self-limiting adverse reactions (e.g., injection site pain, fever) in approximately 17% of participants.
- No Grade 3 or worse adverse events were reported.
- Robust neutralizing antibody titers were observed, ranging from 102.2 to 1065.5 at 28 days post-third dose, and maintained at 14.3 to 218.2 at 180 days.
- The 3-5 year old cohort showed significantly higher antibody titers compared to older cohorts.
- No detectable antibody responses were found in placebo groups.
Conclusions:
- WIBP-CorV is safe, well-tolerated, and elicits robust humoral immunity against SARS-CoV-2 in children aged 3-17 years.
- The vaccine-induced immune response persisted for at least six months post-vaccination.
- These findings support the potential of WIBP-CorV as a pediatric COVID-19 vaccine.
Abstract:
Safe and effective vaccines against SARS-CoV-2 for children are urgently needed. Here we aimed to assess the safety and immunogenicity of an inactivated COVID-19 vaccine candidate, WIBP-CorV, in participants aged 3-17 years. A randomized, double-blind, placebo-controlled, phase 1/2 clinical trial was conducted in Henan Province, China, in healthy children aged 3-17 years. 240 participants in phase 1 trial and 576 participants in phase 2 trial were randomly assigned to vaccine or control with an age de-escalation in three cohorts (3-5, 6-12 and 13-17 years) and dose-escalation in three groups (2.5, 5.0 and 10.0μg/dose), and received 3 intramuscular injections at day 0, 28, and 56. WIBP-CorV showed a promising safety profile with approximately 17% adverse reactions within 30 days after injection and no grade 3 or worse adverse events. The most common adverse reaction was injection site pain, followed by fever, which were mild and self-limiting. The geometric mean titers of neutralizing antibody ranged from 102.2 to 1065.5 in vaccinated participants at 28 days after the third vaccination, and maintained at a range of 14.3 to 218.2 at day 180 after the third vaccination. WIBP-CorV elicited significantly higher titers of neutralizing antibody in the cohort aged 3-5 years than the other two cohorts. There were no detectable antibody responses in all alum-only groups. Taken together, our data demonstrate that WIBP-CorV is safe and well tolerated at all tested doses in participants aged 3-17 years, and elicited robust humoral responses against SARS-CoV-2 lasted for at least 6 months after the third vaccination. This study is ongoing and is registered with www.chictr.org.cn, ChiCTR2000031809.
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