Trials / Completed
CompletedNCT06350890
Efficacy and Safety of Berberine Ursodeoxycholate (HTD1801) in Patients With Type 2 Diabetes
A Multicenter, Randomized, Double-blind, Placebo-controlled Phase 3 Study Evaluating the Efficacy and Safety of HTD1801 in Patients With Type 2 Diabetes Mellitus Who Have Poor Glycemic Control After Dietary and Exercise Interventions
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 408 (actual)
- Sponsor
- HighTide Biopharma Pty Ltd · Industry
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
The goal of this clinical study is to evaluate the efficacy and safety of Berberine Ursodeoxycholate (HTD1801) compared to placebo in patients with type 2 diabetes, inadequately controlled with diet and exercise alone.
Detailed description
This Phase 3 randomized, double-blind, placebo-controlled study will evaluate the efficacy and safety of HTD1801 in two phases, a 24-week double-blind phase followed by a 28-week open-label extension. To ensure stabilization of glycemic control, eligible patients will first participate in a 4-week single-blind run-in period where investigators will provide guidance on lifestyle modification, concomitant medications, and procedures for self-monitoring of blood glucose. Following this period, patient eligibility will be reassessed. Eligible patients will then be randomized 2:1 to receive HTD1801 1000 mg twice daily (BID) or placebo for 24 weeks. Patients who complete the double-blind treatment period will enter an open-label extension period where all patients will receive HTD1801 1000 mg BID for an additional 28 weeks.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | HTD1801 | HTD1801 1000 mg administered orally BID as four capsules |
| DRUG | Placebo | Matching placebo administered orally BID as four capsules |
Timeline
- Start date
- 2023-11-05
- Primary completion
- 2024-12-12
- Completion
- 2025-08-04
- First posted
- 2024-04-08
- Last updated
- 2025-12-29
Locations
56 sites across 1 country: China
Source: ClinicalTrials.gov record NCT06350890. Inclusion in this directory is not an endorsement.