Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06566248

A Clinical Trial to Evaluate the Efficacy and Safety of TQA3810 Tablets in Combination/Non Combination With Nucleoside (Acid) Analogues in Patients With Primary/Treated Chronic Hepatitis B

Randomized, Double-blind, Placebo-controlled Phase IIa Trial to Evaluate the Efficacy and Safety of Combined/Uncombined Nucleoside (Acid) Analogues of TQA3810 Tablets in Primary/Treated Patients With Chronic Hepatitis B

Status
Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
90 (estimated)
Sponsor
Chia Tai Tianqing Pharmaceutical Group Co., Ltd. · Industry
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

To evaluate the efficacy and safety of combined/uncombined nucleoside (acid) analogues of TQA3810 tablets.

Conditions

Interventions

TypeNameDescription
DRUGTQA3810 tablets+NUCTQA3810 is a novel, effective and highly selective small-molecule oral Toll-like receptors-8 agonist.
DRUGPlacebo+NUCNUC: Entecavir Dispersible Tablets, Inhibit viral replication; Tenofovir Disoproxil Fumarate Tablets, Nucleotide reverse transcriptase inhibitors; Tenofovir Alafenamide Fumarate Tablets, Inhibit HBV replication.

Timeline

Start date
2024-03-20
Primary completion
2024-09-01
Completion
2025-03-01
First posted
2024-08-22
Last updated
2024-08-22

Locations

6 sites across 1 country: China

Source: ClinicalTrials.gov record NCT06566248. Inclusion in this directory is not an endorsement.