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A phase 3, randomized, double-blind, placebo-controlled study evaluating the safety and tolerability of HSK31679 compared to placebo in patients with metabolic dysfunction-associated steatohepatitis (MASH) .
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| HSK31679 dose | Experimental | HSK31679 tablet, orally, once daily |
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| Placebo | Placebo Comparator |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| HSK31679 | Drug | tablet |
| |
| Placebo |
| Measure | Description | Time Frame |
|---|---|---|
| Number of Participants With Resolution of Steatohepatitis Without Worsening of Fibrosis at Week 52. | Resolution of steatohepatitis is defined as total absence of ballooning (score=0) and absent or mild inflammation (score 0 to 1). Worsening of fibrosis is defined as progression of fibrosis by ≥1 stage. | Week 52 |
| Number of Participants With at Least an Improvement of Fibrosis ≥1 Stage Without Worsening of Steatohepatitis at Week 52. | Worsening of steatohepatitis is defined as increase in non-alcoholic fatty liver disease (NAFLD) Activity Score (NAS) for ballooning, inflammation, or steatosis. | Week 52 |
| Time to First Occurrence of Disease Progression | Final analysis of the time to first occurrence of disease progression will be measured by a composite of protocol-specified clinical events | Up to 4.5 years |
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Key Inclusion Criteria:
Key Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| fangqiong li | Contact | 028-67258840 | lifangq@haisco.com |
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| ID | Term |
|---|---|
| D065626 | Non-alcoholic Fatty Liver Disease |
| ID | Term |
|---|---|
| D005234 | Fatty Liver |
| D008107 | Liver Diseases |
| D004066 | Digestive System Diseases |
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| Drug |
Matching tablet |
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