Clinical Trials Directory

Trials / Completed

CompletedNCT06171880

To Evaluate the Safety and Pharmacokinetic Characteristics After the Administration of JC-001 and JLP-1901

An Open-label, Randomized, Single Administration, Full Replicated Crossover Phase 1 Clinical Trial to Compare Pharmacokinetics and Safety Between JLP-1901 and JC-001 in Healthy Subjects

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
48 (actual)
Sponsor
Jeil Pharmaceutical Co., Ltd. · Industry
Sex
All
Age
19 Years – 65 Years
Healthy volunteers
Accepted

Summary

To evaluate the safety and pharmacokinetic characteristics after the administration of JC-001 and JLP-1901

Detailed description

An open-label, randomized, single administration, full replicated crossover phase 1 clinical trial to compare pharmacokinetics and safety between JLP-1901 and JC-001 in healthy subjects

Conditions

Interventions

TypeNameDescription
DRUGJLP-1901administration of JLP-1901
DRUGJC-001(active comparator)administration of JC-001(tenofovir)

Timeline

Start date
2022-02-15
Primary completion
2022-03-11
Completion
2022-05-13
First posted
2023-12-15
Last updated
2023-12-15

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT06171880. Inclusion in this directory is not an endorsement.

To Evaluate the Safety and Pharmacokinetic Characteristics After the Administration of JC-001 and JLP-1901 (NCT06171880) · Clinical Trials Directory