Status:
RECRUITING
Trial of CS060380 Tablets for Non-alcoholic Steatohepatitis (NASH)
Lead Sponsor:
Cascade Pharmaceuticals, Inc
Conditions:
NASH
Eligibility:
All Genders
18-70 years
Phase:
PHASE2
Brief Summary
The goal of this clinical trial is to learn if CS060380 tablets works to treat non-alcoholic steatohepatitis(NASH) in adults.It will also learn about the safety of CS060380 tablets.The main questions ...
Detailed Description
This is a multicenter, randomized, double-blind, parallel-group, placebo-controlled Phase IIa clinical trial to evaluate CS060380 tablets in patients with non-alcoholic steatohepatitis (NASH). Subjec...
Eligibility Criteria
Inclusion
- Men or women aged 18 to 70 (including the boundary value).
- Liver biopsy results within 6 months prior to randomization were consistent with the pathological diagnosis of NASH, and the non-alcoholic fatty liver disease activity score (NAS) was ≥4 points, with at least 1 point each for inflammation and balloon changes, and the fibrosis stage of the Clinical Study Network for Non-alcoholic Steatohepatitis (NASH-CRN) in the United States was F1-F3; Or magnetic resonance proton density fat content measurement (MRI-PDFF) within 3 months prior to randomization confirmed that the liver fat content was ≥10%.
- Participants with fertility and their spouses or partners voluntarily took effective contraceptive measures from screening to within 3 months after the last administration. Among them, women of childbearing age include premenopausal women and women within two years after menopause, except those who have undergone hysterectomy or bilateral oophorectomy or have medically confirmed ovarian failure.
- Stable ALT and AST results before randomization. If the ALT or AST value during the screening period is greater than 1.5× upper limit of normal (ULN), there must be two consecutive stable evidences before randomization (with an interval of at least 2 weeks between the two evaluations), and one of the following evidences must be met:
- Compared with the historical data within 2 weeks to 3 months before randomization (if any, and the value ≤5×ULN), the ALT or AST value during the screening period needs to increase by ≤30% compared with the historical data.
- If there is no available historical data and the ALT or AST value during the screening period is greater than 1.5×ULN, the test should be repeated at least once every two weeks. The ALT or AST value after re-testing should increase by no more than 30% compared to the screening period.
- Avoid strenuous exercise at least 24 hours before each visit or blood draw.
- Sign the ICF before the experiment and be able to complete the research as required by the protocol.
Exclusion
- The following liver diseases or past medical history were present at the time of screening:
- Patients with other clinically significant acute or chronic liver diseases or biliary tract diseases not caused by NASH, and the researchers determined that not suitable to participate in this study, Including but not limited to hepatitis B virus, Untreated hepatitis C virus, DILI, ALD, WD, AIH, PBC, PSC.
- Has a history of liver cirrhosis.
- Primary liver cancer. AFP \> 50 μg/L.
- During screening, the following medical history was present:
- Study the history of allergies to drug ingredients and excipients.
- Surgical procedures that may interfere with treatment, including but not limited to weight loss surgery, liver transplantation surgery, etc.
- Screen those who have a history of malignant tumors within the previous five years.
- Contraindications for any MRI scan.
- Screen for a history of drug or substance abuse within the previous two years.
- Screen for a history of heavy drinking for more than three consecutive months within one year prior to the screening.
- Weight change ≥ 5% in the first 3 months of randomization or ≥ 10% in the first 6 months of randomization.
- Individuals who have donated blood within the past 3 months prior to screening, and those who have lost a total of 400 mL or more due to blood donation or other reasons within the past 6 months.
- Merge with any of the following serious cardiovascular disease or surgical histories (including but not limited to):
- Unstable angina pectoris occurred within 3 months prior to randomization.
- Combined heart failure, NYHA ≥ Ⅲ
- Myocardial infarction, shock or life-threatening arrhythmia occurred within 6 months prior to randomization.
- Randomized coronary artery bypass grafting surgery or percutaneous coronary intervention within the first 6 months.
- The following concomitant diseases or conditions occur during the screening period:
- T1DM, uncontrolled T2DM (HbA1c \> 9 % ), history of severe hypoglycemia.
- Intestinal diseases that affect the absorption of oral medications.
- There are thyroid diseases, including hyperthyroidism and hypothyroidism or pituitary disorders.
- Combined with serious diseases such as circulatory, respiratory, urinary, hematological, immune, psychiatric, neurological, and renal disorders, it has been determined by the researchers that it is not suitable to participate in this study.
- Uncontrolled hypertension was present during screening: systolic blood pressure \>160mmHg or diastolic blood pressure \>100mmHg even under regular medication control.
- When screening QTcF \>450 ms (for males) or \>470 ms (Female).
- When screening, HIV antibody positive and syphilis spiral antibody positive.
- Pregnant and lactating women.
- Laboratory test:
- PLT\<LLN.
- TBIL \> 1.2×ULN, Gilbert Syndrome.
- ALT or AST \> 5 × ULN.
- eGFR \< 50 mL/min/1.73 m².
- IRN \> 1.5.
- THS or FT4 abnormality.
- Cardiac Troponin \> ULN.
- The following medication history existed before randomization:
- No stable dose of sodium-glucose cotransporter-2 was received within 6 months prior to randomization(SGLT2).
- Use of an excessively high dose of vitamin E within 6 months prior to randomization (unless the dose is stable and \<400 IU/d), pioglitazone, glucagon-like peptide-1 (GLP-1) receptor agonists GIPR/GLP-1R dual agonists, GIPR/GLP-1R/GCGR triple agonists, compound Oral antidiabetic (OAD) regimens (three or more OADs).
- Those who have received treatment for NAFLD/NASH including but not limited to the following within 3 months prior to randomization Drugs, FXR agonists, FGF21 analogues, DGAT2 inhibitors, PDE inhibitors Agents, other THR-β agonists, obeticholic acid, etc.
- Within 3 months prior to randomization (for unmarketed drugs or devices) or within 5 half-lives (for marketed drugs), the patient has participated in other investigational product or device clinical trials (if there is evidence that the patient participated in a clinical trial, received treatment in the inactive drug group, or has been removed from the group without receiving treatment with the investigational product, they are eligible to participate in this study for screening).
- Having received drug treatment that includes but is not limited to the following drugs that may cause NAFLD/NASH for at least 2 weeks within one month prior to boarding the machine For example, total parenteral nutrition (TPN), amiodarone, methotrexate, systemic glucocorticoids, tetracycline, tamoxifen, estrogen with doses greater than those used for contraception or hormone replacement, anabolic steroids, valproic acid and other known liver-toxic drugs.
- Within 4 weeks prior to randomization or during the intended clinical study period, liver-protecting drugs not permitted by the protocol were used, including but not limited to silymarin (bin), bicyclol, glycyrrhizic acid preparations (magnesium isoglycyrrhizinate, compound glycyrrhizin, diammonium glycyrrhizinate, etc.).
- Received anticoagulant treatment within 2 weeks prior to randomization: drugs that increase INR (e.g., FXa inhibitors, warfarin, heparin, etc.).
- Those who have used CYP3A enzyme strong suppressors, CYP3A enzyme strong inducers, inhibitors of P-gp or BCRP transporters that may affect the metabolism or absorption of this drug within 14 days prior to randomization or at least 5 half-lives (whichever is longer).
- Other circumstances that the researcher deems unsuitable for inclusion in the trial.
Key Trial Info
Start Date :
September 30 2025
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
May 6 2026
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT07198386
Start Date
September 30 2025
End Date
May 6 2026
Last Update
November 24 2025
Active Locations (4)
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1
The First Affiliated Hospital of Fujian Medical University
Fuzhou, Fujian, China
2
Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine
Shanghai, Shanghai Municipality, China
3
Zhongshan Hospital Fudan University
Shanghai, Shanghai Municipality, China
4
The Affiliated Hospital of Hangzhou Normal University
Hangzhou, Zhejiang, China, 311121