Homologous Booster Study of COVID-19 Protein Subunit Recombinant Vaccine

NCT05933278 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 150

Last updated 2025-06-05

No results posted yet for this study

Summary

Open-label, prospective intervention study of IndoVac® as a single, homologous booster dose

Conditions

Interventions

BIOLOGICAL

SARS-CoV-2 Subunit Recombinant Protein Vaccine

SARS-CoV-2 RBD subunit recombinant protein, manufactured by PT Bio Farma

Sponsors & Collaborators

  • PT Bio Farma

    lead INDUSTRY

Principal Investigators

  • Yetty Movieta Nency, MD · Faculty of Medicine Universitas Diponegoro

Study Design

Allocation
NA
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-07-25
Primary Completion
2024-08-31
Completion
2024-09-05

Countries

  • Indonesia

Study Locations

More Related Trials

Entities

Diseases

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 NCT05933278 on ClinicalTrials.gov