Clinical Trials Directory

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UnknownNCT02966964

A Clinical Trials to Evaluate the Efficacy and Safety of Tenofovir With and Without DWPUR001 in Patients With HBV

An Exploratory, Randomized, Double-blinded, Placebo-controlled Study to Evaluate the Efficacy and Safety of Tenofovir With and Without DWPUR001 in Patients With Hepatitis B Virus(HBV)

Status
Unknown
Phase
Phase 2
Study type
Interventional
Enrollment
90 (estimated)
Sponsor
Uijeongbu St. Mary Hospital · Academic / Other
Sex
All
Age
19 Years – 69 Years
Healthy volunteers
Not accepted

Summary

The patient who meets the inclusion/exclusion criteria is assigned to Test1 group or Test 2 group or control group randomly. All subjects take one pill of Viread® Tab. (Tenofovir Disoproxil Fumarate 300mg) once a day for 48 weeks. At the same time, all randomized subjects take two pills of DWPUR001 or Placebo of DWPUR001 twice a day for 48 weeks.

Conditions

Interventions

TypeNameDescription
DRUGDWPUR001
DRUGPlacebo

Timeline

Start date
2015-04-01
Primary completion
2018-11-01
Completion
2019-02-01
First posted
2016-11-17
Last updated
2017-09-25

Locations

6 sites across 1 country: South Korea

Source: ClinicalTrials.gov record NCT02966964. Inclusion in this directory is not an endorsement.