Clinical Trial to Evaluate the Safety and Efficacy of NTCB02-1 in Patients Who Require Parenteral Nutrition

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age19+
SponsorYuhan Corporation

About this trial

A Randomized, Open-labeled, Multi-center, Active-controlled, Parallel-group Phase 3 Clinical Trial to Evaluate the Safety and Efficacy of NTCB02-1 versus NTCB-C in patients who require parenteral nutrition

Eligibility criteria

Qualifiers

Those who are 19 years old or older at the screening visit

Patients are expected to require PN for more than 3 days

Patients who voluntarily signed the consent form

Disqualifiers

Patients are expected difficult to survive more than 3 days

Patients BMI is over 30 kg/m2

Patients having hypersensitivity to any peanut-, fish-, soy-, egg protein, or investigational drug

Patients with difficult central venous line

Trial design

Treatments tested in this trial

  • NTCB02-1
  • NTCB-C

Treatment groups

60 Participants
are divided into 2 treatment groups

Sponsors and collaborators