A Clinical Trial of BGT-002 Tablets in Subjects With Nonalcoholic Steatohepatitis

NCT ID: NCT06491576

Last Updated: 2024-07-09

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 48 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-03-21
• Study Completion Date: 2024-03-04

Brief Summary

This study is a single-center, randomized, double-blind, multiple ascending doses (MAD), placebo-controlled phase Ib/IIa clinical trial of BGT-002 Tablets in subjects with NASH to evaluate the safety, tolerability, pharmacokinetics (PK) and early pharmacodynamics (PD) of BGT-002 Tablets.

Conditions

NASH

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Test Group

Group Type: EXPERIMENTAL

BGT-002

Intervention Type: DRUG

taking the study drug orally

Placebo Group

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

taking the placebo orally

Interventions

BGT-002

taking the study drug orally

Intervention Type: DRUG

Placebo

taking the placebo orally

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Subjects aged ≥ 18 and ≤ 65, male or female;
• Body mass index (BMI) ≥ 25 kg/m^2 at screening;
• Subjects fulfilling the following criteria:
• ALT level exceeds the upper limit of normal once within 3 months (ALT elevation without other obvious reasons);
• Mean liver fat content ≥ 10% during screening and at the end of the run-in period (MRI-PDFF);
• Stable body weight (defined as weight gain or loss ≤ 5%) 4-8 weeks pre-dose;
• Pre-dose blood pressure: Systolic blood pressure ≤ 160 mmHg and diastolic blood pressure ≤ 95 mmHg (oral antihypertensive drugs can be taken regularly);
• Maintain the same medication and lifestyle (diet and/or exercise) as those at enrollment during the trial;
• Subjects who have no birth plan from screening to 6 months after the last dose and voluntarily take reliable contraceptive measures;
• Subjects who fully understand the purpose and requirements of the trial, voluntarily participate in the clinical trial, and sign the written ICF, and are able to complete all trial processes according to the trial requirements.

Exclusion Criteria

• Subjects with a known history of allergies to the test product, any of its components, or related products; as well as those with allergic diseases or an allergic constitution;
• Subjects with heavy alcohol consumption for 3 consecutive months or above within 1 year before screening. "Heavy alcohol consumption" is defined as average daily alcohol consumption of > 20 g for females and > 30 g for males, or uncontrollable alcohol consumption;
• Subjects with cirrhosis suggested by liver biopsy or clinically diagnosed cirrhosis;
• Subjects with other concomitant liver diseases, including but not limited to drug-induced liver disease, alcoholic liver disease, autoimmune liver disease, hemochromatosis, Wilson's disease, suspected or confirmed liver cancer;
• Subjects who have received liver transplantation surgery or plan to have this surgery:
• Subjects who have received bariatric surgery or plan to have this surgery during the study;
• Subjects with type 1 diabetes and poorly controlled type 2 diabetes (HbA1c > 10.5% at screening);
• Patients with diabetes who use hypoglycemic drugs other than metformin;
• Subjects with a history of malignant tumor within 5 years before screening (Note: 1. Subjects with cervical carcinoma in situ whose lesions have been resected and with no evidence of recurrence or metastasis for at least 3 years may participate in this study. 2. Subjects with basal cell or squamous cell carcinoma whose lesions have been completely resected and with no recurrent lesions for at least 3 years can participate in this study;
• Subjects with serious cardiovascular and cerebrovascular events within 6 months before screening, including but not limited to uncontrolled or serious arrhythmia (ventricular fibrillation, atrial fibrillation, etc.), angina unstable, acute myocardial infarction, cardiac failure congestive, coronary intervention (including coronary artery stent implantation, intracoronary thrombectomy, and percutaneous transluminal coronary angioplasty, etc) or coronary artery bypass surgery, peripheral vascular intervention, stroke (except lacunar infarction), and transient ischaemic attack;
• Subjects with gastrointestinal diseases or postoperative conditions affecting drug absorption;
• Subjects who are taking drugs that may cause steatosis/steatohepatitis;
• Subjects who have used ACLY-targeted drugs (Nexletol, etc.) and other study drugs, are taking statins (lovastatin, simvastatin, pravastatin, mevastatin, fluvastatin, atorvastatin, cerivastatin, rosuvastatin, pitavastatin, etc.), fibric acids (such as fenofibrate, gemfibrozil), probucol, warfarin, systemic steroids, cyclosporin or other immunosuppressants, or have taken these drugs less than 1 month or 5 half-lives of the drug (whichever is longer) from the first administration of the study drug;
• Subjects who have used drugs with potential therapeutic effects on NASH (such as GLP-1 receptor agonists, DPP4 inhibitors, SGLT2 inhibitors, or other drugs known to affect liver function and cause steatosis at the discretion of the investigator) during the trial period and within less than 1 month from the screening;
• Subjects with a TG > 6.0 mmol/L, direct bilirubin > 2 × ULN, creatinine clearance < 60 mL/min (calculated using the Cockcroft-Gault formula);
• Platelet count < 75 × 10^9/L;
• Subjects with confirmed positive and clinically significant results for antinuclear antibody (ANA) at screening;
• Subjects with a history of hypothyroidism, hyperthyroidism, or subclinical thyroid disease (except for those with TSH levels < 10 mu/l, normal free T3 and T4 levels, and no symptoms of hypothyroidism);
• Subjects with contraindications to MRI scan;
• Subjects with blood donation or blood loss ≥ 400 mL within 3 months before screening;
• Subjects who have participated in other drug clinical trials within 1 month prior to the screening;
• Pregnant/lactating women or subjects confirmed positive in serum pregnancy test (female);
• Subjects with positive results in urinary drug screening (morphine, marijuana);
• Subjects who have consumed any food or beverage containing alcohol (or positive alcohol breath test result), grapefruit juice/grapefruit juice, methylxanthine (such as coffee, tea, cola, chocolate, and energy drink) within 1 day pre-dose, or have strenuous exercise or other factors affecting drug absorption, distribution, metabolism, and excretion;
• Subjects with other severe systemic diseases unrelated to NASH;
• Subjects infected with viral hepatitis (including hepatitis B and C), AIDS, or syphilis;
• Subjects with high-risk factors of torsades de pointes (hypokalemia, hypomagnesemia, heart rate < 45 bpm), and ECG QTc interval longer than 490 ms during screening;
• Subjects with other factors deemed by investigators as not suitable for the trial.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Burgeon Therapeutics Co., Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Ding Yanhua, Doctor

Role: PRINCIPAL_INVESTIGATOR

The First Hospital of Jilin University

Locations

The First Bethune Hospital of Jilin University

Changchun, Jilin, China

Countries

China

Provided Documents

Document Type: Study Protocol

View Document

Document Type: Statistical Analysis Plan

View Document

Other Identifiers

BGT-002-004

Identifier Type: -

Identifier Source: org_study_id