At a glance
ClinicalIndex Comparison RecordPhase 3Completed· 230 enrolled
Drug / intervention
Immuncell-LCbiological
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Randomized, Open-label, Multi-center and Phase 3 Clinical Trial to Compare the Efficacy and Safety of 'Green Cross CELL Immuncell-LC Group' and 'Non-treatment Group' in Patient Undergone Curative Resection(PEIT, RFA or Operation) for Hepatocellular Carcinoma in Korea
In Brief
A Phase 3 clinical trial evaluating Immuncell-LC for Hepatocellular Carcinoma. Completed, enrolled 230 participants across 5 sites.
Detailed Summary
To prove that the efficacy and safety of 'Green Cross CELL\* Immuncell-LC group' is superior to 'non-treatment group(Control group)' in patient undergone curative resection(PEIT, RFA or operation) for hepatocellular carcinoma in Korea
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHepatocellular Carcinoma
CountriesSouth Korea
Collaborators--
Timeline
Phase 3CompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedJun 2008
Enrollment StartJul 2008
Primary CompletionNov 2012
TodayJul 2026
First PostedJun 18, 2008
Enrollment StartJul 1, 2008
Primary CompletionNov 1, 2012
TodayJul 2, 2026
Enrollment to primary: 4.3 yearsPosted 18.0 years ago
Interventions
Immuncell-LCbiological
Activated T lymphocyte