Clinical Trial to Evaluate the Safety and Efficacy of NTCB01-1 in Patients Who Require Parenteral Nutrition
NCT06625931 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 60
Last updated 2025-05-15
Summary
A Randomized, Open-labeled, Multi-center, Active-controlled, Parallel-group Phase 3 Clinical Trial to Evaluate the Safety and Efficacy of NTCB01-1 versus NTCB-P in patients who require parenteral nutrition
Conditions
- Parenteral Nutrition
Interventions
- DRUG
-
NTCB01-1
3 Days infusion
- DRUG
-
NTCB-P
3 Days infusion
Sponsors & Collaborators
-
Yuhan Corporation
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 19 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-11-14
- Primary Completion
- 2025-03-28
- Completion
- 2025-03-28
Countries
- South Korea
Study Locations
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