This study is a multicenter, open-label, dose-escalation trial designed to evaluate the safety, tolerability, PK, and PD profiles of ACT500 in participants with metabolic dysfunction-associated steatotic liver disease (MASLD). The trial plans to enroll approximately 24 MASLD participants across four dose cohorts, each consisting of 6 participants who will receive oral ACT500 once daily.
The participant fully understands the purpose, nature, methods, and possible adverse reactions of the study, voluntarily participates in this study, and has signed the informed consent form.
Male or female participants aged between 18 and 69 years (inclusive of 18 and 69 years) at the time of signing the informed consent form.
Liver fat content (LFC) ≥10% as assessed by magnetic resonance imaging-proton density fat fraction (MRI-PDFF) during the screening period.
Liver stiffness measurement (LSM) assessed by FibroScan during the screening period meets the criteria of 8 kPa ≤ LSM ≤ 15 kPa, OR a liver biopsy pathological result of F2/F3 fibrosis within 6 months prior to screening.
[1] Combined with other liver diseases, including but not limited to hepatitis B, hepatitis C, drug-induced liver disease, alcoholic liver disease, autoimmune liver disease, suspected or confirmed hepatocellular carcinoma, etc.
Sequential
ACT500 tablets
DrugOnce daily, orally
Adverse Event#AE#
Serious Adverse Event
body temperature
Number of participants with treatment-related adverse events as assessed by NCI-CTCAE v6.0
Area Under Curve（0-t）
Area Under the Concentration-time curve from time zero to τ at steady state
Area Under Curve（0-∞）
Maximum Plasma Concentration
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Xiamen Amoytop Biotech Co., Ltd.
Lead sponsor
Beijing Tsinghua Changgeng Hospital
Collaborator
This trial is not recruiting at the moment. You can still explore other options:
