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Study identifier: NCT07128797 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

a Safety, Tolerability, and Pharmacokinetic Trial of Multiple Subcutaneous Injections of B1344 Injection in Patients With Nonalcoholic Fatty Liver Disease(NAFLD)

Condition: NAFLD (Non-alcoholic Fatty Liver Disease) · NASH (Nonalcoholic Steatohepatitis)  ·  Sponsor: Tasly Biopharmaceuticals Co., Ltd.

PhasePhase 1
Planned participants32
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

This is a randomized, double-blind, multicenter, placebo-controlled, multiple-dose escalating clinical trial designed to evaluate the safety, tolerability, pharmacokinetics, and immunogenicity profile of B1344 in patients with NAFLD. Additionally, the trial will conduct preliminary observations on the efficacy of B1344, aiming to provide early proof of concept for B1344 as a therapeutic agent for NASH.

This description comes directly from the study's public registry record.

Talk to the study team

Lai Wei  ·  13601281862  ·  weilai@mail.tsinghua.edu.cn

Always discuss trial participation with your own doctor first.

Locations (5)

Beijing Tsinghua Changgung Hospital (BTCH) affiliated to Tsinghua UniversityBeijing, Beijing Municipality, ChinaRecruiting
Nanfang Hospital, Southern Medical UniversityGuangzhou, Guangdong, ChinaNot Yet Recruiting
Sinopharm Tongmei General HospitalDatong, Shanxi, ChinaNot Yet Recruiting
The First Affiliated Hospital to Nankai UniversityTianjin, Tianjin Municipality, ChinaNot Yet Recruiting
The First Affiliated Hospital to Wenzhou Medical UniversityWenzhou, Zhejiang, ChinaNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT07128797