Clinical Trials Directory

Trials / Active Not Recruiting

Active Not RecruitingNCT06706310

Evaluate TQ-A3334 Combined Nucleoside (Acid) Analogs in the First Treatment/Treatment of Chronic HBV Infection

Evaluate TQ-A3334 Tablets Combined Nucleoside (Acid) Analogs in the Initial Treatment/Chronic Hepatitis B Virus (HBV) Infection Subjects of Chronic HBV Infection

Status
Active Not Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
116 (estimated)
Sponsor
Chia Tai Tianqing Pharmaceutical Group Co., Ltd. · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

This study uses random, double -blindness, placebo control, and phase multi -center test design. All subjects who meet the standards receive TQ-A3334 per tablet/placebo nucleoside (acid) analog. A total of 116 subjects are needed.

Conditions

Interventions

TypeNameDescription
DRUGPlaceboPlacebo contains no active substance.
DRUGTQA3334 TabletInhibit viral replication.
DRUGNucleoside (acid) analogs (NAs)Inhibit viral replication.

Timeline

Start date
2024-12-04
Primary completion
2025-06-22
Completion
2026-06-01
First posted
2024-11-26
Last updated
2025-11-26

Locations

15 sites across 1 country: China

Source: ClinicalTrials.gov record NCT06706310. Inclusion in this directory is not an endorsement.