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

NCT06491576 | Completed Phase 1

• 1 other identifier: BGT-002-004
• Study Type: interventional
• Target: 48
• Locations: 1 country
• Sites: 1

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

Outcome Measures

Primary Outcomes (2)

• Number of participants with adverse events

  From Day 1 to Day 56

• C-QTc(Concentration-QTc)

  To investigate the effect of BGT-002 on QT/QTc interval in subjects

  Day1、Day28

Secondary Outcomes (18)

• Cmax(Peak Concentration)

  Day1

• Tmax(Time of maximum observed concentration)

  Day1

• AUC(0-24h)(Area Under Curve)

  Day1

• Cmax,ss

  Day28

• Tmax,ss

  Day28

Study Arms (2)

Test Group

EXPERIMENTAL

Drug: BGT-002

Placebo Group

PLACEBO COMPARATOR

Drug: Placebo

Interventions

BGT-002 DRUG

taking the study drug orally

Test Group

Placebo DRUG

taking the placebo orally

Placebo Group

Eligibility Criteria

• Age: 18 Years - 65 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• 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.

You may not qualify if:

• 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);

Sponsors & Collaborators

• Burgeon Therapeutics Co., Ltd.: lead

Study Sites (1)

The First Bethune Hospital of Jilin University

Changchun, Jilin, 130031, China

Location

Study Officials

• Ding Yanhua, Doctor

  The First Hospital of Jilin University

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: QUADRUPLE
• Who Masked: PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: May 30, 2024
• First Posted: July 9, 2024
• Study Start: March 21, 2023
• Primary Completion: March 4, 2024
• Study Completion: March 4, 2024
• Last Updated: July 9, 2024

Record last verified: 2024-06

Data Sharing

• IPD Sharing: Will not share

Locations

CN (1)