A Study to Evaluate the Immunogenicity and Safety of SCTV01C and SCTV01E (Two Recombinant Protein COVID-19 Vaccines) in Population Aged ≥12 Years

NCT05308602 · Status: WITHDRAWN · Phase: PHASE2 · Type: INTERVENTIONAL

Last updated 2024-02-09

No results posted yet for this study

Summary

The objective of the study is to evaluate the immunogenicity and safety of SCTV01C or SCTV01E, comparing the immunogenicity data against Beta (B.1.351), Delta (B.1.617.2), Omicron (B.1.1.529) and other variants with Sinopharm inactivated COVID-19 vaccine or mRNA vaccine.

Conditions

Interventions

BIOLOGICAL

SCTV01C

Day 0; intramuscular injection

BIOLOGICAL

SCTV01C

Day 28; intramuscular injection

BIOLOGICAL

SCTV01C

Day 180; intramuscular injection

BIOLOGICAL

SCTV01E

Day 0; intramuscular injection

BIOLOGICAL

SCTV01E

Day 28; intramuscular injection

BIOLOGICAL

SCTV01E

Day 180; intramuscular injection

BIOLOGICAL

mRNA vaccine manufactured by Pfizer or Moderna

Day 0; intramuscular injection

BIOLOGICAL

mRNA vaccine manufactured by Pfizer or Moderna

Day 28; intramuscular injection

BIOLOGICAL

mRNA vaccine manufactured by Pfizer or Moderna

Day 180; intramuscular injection

BIOLOGICAL

Sinopharm inactivated COVID-19 vaccine

Day 0; intramuscular injection

BIOLOGICAL

Sinopharm inactivated COVID-19 vaccine

Day 28; intramuscular injection

BIOLOGICAL

Sinopharm inactivated COVID-19 vaccine

Day 180; intramuscular injection

Sponsors & Collaborators

  • Sinocelltech Ltd.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
12 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-04-01
Primary Completion
2022-08-01
Completion
2023-08-01

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05308602 on ClinicalTrials.gov