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
| Type | Name | Description |
|---|---|---|
| DRUG | TQA3810 tablets+NUC | TQA3810 is a novel, effective and highly selective small-molecule oral Toll-like receptors-8 agonist. |
| DRUG | Placebo+NUC | NUC: 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.