Clinical Trial to Evaluate the Safety and Efficacy of NTCB02-1 in Patients Who Require Parenteral Nutrition
← catalyst calendarSponsored by Yuhan Corporation (industry) · 000100.KS — their whole pipeline →.
Phase
Phase 3
Status
Recruiting
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
60estimated
Sites
5
Country
South Korea
Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →
Source: ClinicalTrials.gov, retrieved 2026-08-19
Dates
each axis at the precision it was filed, with the registry's own basis| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2024-12-04 | actual | When the study began enrolling |
| Primary completion | 2025-07-18 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2025-07-18 | estimated | The whole study's end, after follow-up |
| First posted | 2024-10-03 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2025-01-07 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Parenteral Nutrition
Interventions
- Drug: NTCB02-1
- Drug: NTCB-C
Primary outcome
what the primary-completion date above is the date OFOccurance rate of adverse drug reaction
measured Day 1 to day 4
Permalink · 000100.KS's whole pipeline · Catalyst calendar · Every registered study · What changed