drugset / Trial / NCT04606329

To Evaluate the Efficacy and Safety of LuminoMark Injection in Patients With Nonpalpable Breast Lesions(Phase 3)

NCT04606329 ↗

Phase 3 Completed 109 enrolled Hanlim Pharm. Co., Ltd.
RandomizedParallel-groupOpen-labelTreatment

Summary

This study is a multicenter, Randomized, Open-label, Parallel, Phase 3 Clinical Trial in 8 weeks for screening, once Investigational product injection, Follow up visit.

Timeline

Start
2020-07-20
Primary completion
2021-01-28
Completion
2021-01-28

Drugs

EvaluationDrugModalityDoseRoute
Comparator Charcotrace Unknown 0.3 ml —
Comparator Charcotrace Unknown 1 ml —
Subject LuminoMark Diagnostic / imaging agent 0.2 ml —

Indications