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NCT04064554

Clinical Study to Evaluate Safety and Immunogenicity of Bacillus Calmette-Guerin (BCG) Delivery Via Novel Micronjet600 Device Compared to Those Via Conventional Needle

Completed NA Last updated 5 December 2019
What this trial tests

NA trial testing BCG vaccination with MicronJet600 in Tuberculosis in 15 participants. Completed in 11 September 2019.

Timeline
1 December 2017
Primary endpoint
11 September 2019
11 September 2019

Quick facts

Lead sponsorYonsei University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposeprevention
Enrollment15
Start date1 December 2017
Primary completion11 September 2019
Estimated completion11 September 2019
Sites1 location across South Korea

Drugs / interventions tested

Conditions studied

Sponsor

Yonsei University

Who can join

Adults 19 to 35, any sex, with Tuberculosis or BCG Vaccination. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to evaluate safety and immunogenicity of Bacillus Calmette-Guerin (BCG) delivery via Novel Micronjet600 device compared to those via conventional needle.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Beyond the Needle: Innovative Microneedle-Based Transdermal Vaccination.
    Nguyen HX. · · 2025 · cited 15× · PMID 39982324 · DOI 10.3390/medicines12010004

Verify or expand the search:

Other recruiting trials for Tuberculosis

Currently open trials in the same condition.

Other Yonsei University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04064554.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing