Multiple under-the-skin injections of B1344 for adults with NAFLD and NASH

A Randomized, Double-Blind, Multi-Center, Placebo-Controlled Phase Ib Clinical Trial to Evaluate the Safety, Tolerability, and Pharmacokinetics of Multiple Subcutaneous Injections of B1344 Injection in Patients With Non-Alcoholic Fatty Liver Disease (NAFLD)

This trial will test whether repeated subcutaneous injections of an experimental drug called B1344 are safe and affect liver fat and related measures in adults with NAFLD or NASH.

Quick facts

• Phase: Phase 1
• Study type: Interventional
• Enrollment: 32 (estimated)
• Ages: 18 Years to 75 Years
• Sex: All
• Sponsor: Tasly Biopharmaceuticals Co., Ltd. (Industry-sponsored)
• Drugs / interventions: methotrexate
• Locations: 5 sites (Beijing, Beijing Municipality and 4 other locations)
• Trial ID: NCT07128797 on ClinicalTrials.gov

What this trial studies

This is a randomized, double-blind, multicenter, placebo-controlled, multiple-dose escalation phase 1 trial designed to characterize safety, tolerability, pharmacokinetics, and immunogenicity of B1344 given by subcutaneous injection. Participants are adult Chinese patients with NAFLD (MRI-PDFF ≥10%) and at least one metabolic risk factor, randomized to receive B1344 or placebo across escalating dose cohorts. The trial will collect serial blood samples for PK and immune response testing, monitor adverse events closely, and make preliminary observations on liver fat and related biomarkers as early proof of concept. Sites are located at major tertiary hospitals in Beijing, Guangzhou, and Datong, China.

Who should consider this trial

Good fit: Ideal candidates are Chinese adults aged 18–75 with NAFLD and MRI-PDFF ≥10% who also have at least one metabolic risk factor such as overweight/obesity, impaired glucose regulation, hypertension, or dyslipidemia.

Not a fit: Patients without significant liver fat (MRI-PDFF <10%), those with advanced liver disease (e.g., cirrhosis), or individuals who cannot attend study visits at the listed Chinese sites are unlikely to benefit from participation.

Why it matters

Potential benefit: If successful, B1344 could offer a new therapeutic option that reduces liver fat or slows progression toward NASH in patients with fatty liver disease.

How similar studies have performed: Other early-phase metabolic and anti-fibrotic agents have shown reductions in liver fat and metabolic markers in short-term trials, but no single therapy is yet established as a definitive cure for NASH so this remains an early-stage approach.

Eligibility criteria

Inclusion Criteria:

1. Chinese patients aged between 18 and 75 years;
2. Patients diagnosed with NAFLD and with a magnetic resonance proton density fat fraction (MRI-PDFF) ≥10% in the screening/baseline period or within one month prior;
3. Presence of any one of the following metabolic risk factors:

   * Body Mass Index (BMI) ≥24.0 kg/m² or abdominal obesity (male waist circumference ≥90 cm, female waist circumference ≥85 cm);
   * Fasting blood glucose ≥6.1 mmol/L, or 2-h blood glucose after glucose load ≥7.8 mmol/L, or glycated hemoglobin (HbA1c) ≥5.7%, or history of type 2 diabetes, or Homeostasis Model Assessment Insulin Resistance Index (HOMA-IR) ≥2.5;
   * Resting blood pressure ≥130/85 mmHg, or currently receiving antihypertensive medication;
   * Fasting serum triglycerides (TG) ≥1.70 mmol/L, high-density lipoprotein cholesterol (HDL-c) ≤1.0 mmol/L (male) and 1.3 mmol/L (female), or currently receiving lipid-lowering medication.
4. Weight stability reported by participants within 6 weeks before enrollment (absolute weight change ≤5%).
5. Participants have no fertility plans within 3 months after signing the informed consent and voluntarily take effective contraceptive measures.
6. Voluntary participation in the clinical trial, able to sign the informed consent, and capable of understanding and complying with the trial procedures.

Exclusion Criteria:

1. Liver biopsy, or clinical diagnosis of cirrhosis based on clinical presentation, biochemical and imaging results, or any of the following criteria: ① FIB-4 score ≥3.48 in the screening/baseline period or within 1 month prior, or liver stiffness value (LSM) ≥15 kPa based on FibroScan; ② liver biopsy results indicating NASH-F4 stage within the previous 24 months; ③ clinical examination signs of liver cirrhosis or splenomegaly during the screening/baseline period; ④ abdominal imaging results showing liver nodules or splenomegaly during the screening/baseline period or within 1 month prior.
2. History of tumors or liver transplantation, or patients planning to undergo liver transplantation.
3. History of liver diseases other than NAFLD or clinical suspicion of liver diseases other than NAFLD, including but not limited to secondary NAFLD, hepatitis B, hepatitis C, autoimmune hepatitis, hemochromatosis, alcoholic liver disease, primary sclerosing cholangitis, primary biliary cholangitis, or Wilson's disease.
4. History of other diabetes besides T2DM (such as type 1 diabetes, secondary diabetes, etc.), or currently using or planning to use insulin, thiazolidinediones, and glucagon-like peptide-1 (GLP-1) analog drugs for treatment.
5. Presence of other severe, progressive, or uncontrolled diseases besides T2DM, hypertension, and dyslipidemia, including but not limited to immune system, endocrine system, hematologic system, urinary system, hepatobiliary system, respiratory system, nervous system, psychiatric system, cardiovascular system, digestive system, where participation in this trial would increase participant risk as determined by the investigator.
6. Previous history of weight-loss surgery or plans for weight-loss during the trial, or significant changes in exercise or dietary habits.
7. History of extra-bone injury, fracture, or bone-related surgery within 2 months before screening.
8. Participants with a history of long QT syndrome or family history of sudden death, or males with QTcF \> 450 ms, females with QTcF \> 470 ms.
9. Allergic to B1344 or its excipients, or history of allergy to other biological products or severe allergic reactions.
10. History of drug use related to secondary NAFLD lasting more than 2 weeks within 12 months before screening, including amiodarone, methotrexate, systemic corticosteroids, 5-fluorouracil, irinotecan, tetracycline, tamoxifen, doses exceeding hormone replacement estrogen, anabolic steroids, valproic acid, and other known hepatotoxic drugs.
11. History of concomitant treatment that does not meet protocol requirements before enrollment, or concomitant treatment that meets protocol requirements but cannot maintain a stable dose until the end of the trial, or plans to initiate new concomitant treatments after the first dose until the end of the trial.
12. Previous use of FGF-21 analogs or FGFR1 agonists.
13. Screening/baseline examination results meeting the following criteria:

    * Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) ≥5 times the upper limit of normal (ULN), total bilirubin \>ULN;
    * Estimated glomerular filtration rate (eGFR) \<60 mL/min/1.73m²;
    * Hemoglobin \<120 g/L (male) or \<110 g/L (female);
    * HbA1c ≥9%; fasting blood glucose ≥13.9 mmol/L;
    * International normalized ratio (INR) \>1.3;
    * Platelet count \<110×10⁹/L;
    * Dual-energy X-ray absorptiometry (DXA) T-score ≤-2.5;
    * Resting systolic blood pressure \<90 or ≥160 mmHg, resting diastolic blood pressure \<50 or ≥100 mmHg;
    * Resting heart rate \<60 or \>100 beats/minute;
    * TG ≥5.65 mmol/L;
    * Hepatitis B surface antigen (HBsAg) positive, hepatitis C antibody (HCVAb) positive, human immunodeficiency virus (HIV) antibody positive, or positive for serum Treponema pallidum specific antibody (TP-Ab).
14. History of long-term excessive alcohol consumption, or alcohol consumption ≥14 World Health Organization (WHO) alcohol units per week (1 WHO alcohol unit = 10 g pure alcohol) within 3 months before screening, or positive alcohol screening, or unable to refrain from alcohol 48 hours before the first dose until the end of the trial.
15. Excessive consumption of tea, coffee, or caffeinated beverages (daily consumption of more than 8 cups of respective drinks, with 1 cup being 250 mL) within 3 months before screening, or consumption of any caffeinated food or drink (such as coffee, strong tea, chocolate, cola, etc.) within 48 hours before the first dose.
16. History of blood donation, loss of blood ≥200 mL, blood transfusion, or use of blood products within 3 months before screening, or plans to donate blood during the trial.
17. History of needle phobia, blood phobia, or frequent episodes of orthostatic hypotension, or inability to tolerate venipuncture.
18. History of drug abuse, or positive urine drug abuse screening.
19. Smoking more than 5 cigarettes daily within the last 3 months or cannot completely quit smoking during the trial.
20. Women who are pregnant or breastfeeding, or planning to become pregnant or breastfeed during the trial.
21. Any skin or abdominal wall anomalies that would affect subcutaneous injection, or tattoos or scars covering more than 50% of the abdominal wall surface area.
22. Participation in other clinical trials and receiving trial interventions within the last 3 months.
23. Existing MRI examination contraindications or inability to cooperate with MRI examinations before screening.
24. Other circumstances deemed unsuitable for participation in this trial by the investigator.

Where this trial is running

Beijing, Beijing Municipality and 4 other locations

• Beijing Tsinghua Changgung Hospital (BTCH) affiliated to Tsinghua University — Beijing, Beijing Municipality, China (Recruiting)
• Nanfang Hospital, Southern Medical University — Guangzhou, Guangdong, China (Not_yet_recruiting)
• Sinopharm Tongmei General Hospital — Datong, Shanxi, China (Not_yet_recruiting)
• The First Affiliated Hospital to Nankai University — Tianjin, Tianjin Municipality, China (Not_yet_recruiting)
• The First Affiliated Hospital to Wenzhou Medical University — Wenzhou, Zhejiang, China (Not_yet_recruiting)

Study contacts

• Study coordinator: Lai Wei

Conditions NAFLD; NASH