Clinical trials

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Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

A Study of CS060380 Tablets in Patients With MASH and Obesity

this study is looking at a new investigational medicine called CS060380, when used together with semaglutide, in adults who have both metabolic dysfunction-associated steatohepatitis (MASH) and obesity. MASH is a condition where too much fat builds up in the liver, leading to inflammation and damage. Obesity is a major risk factor for this condition. This is a Phase II clinical trial, which means we are testing the medicine to see if it works and is safe. The study will last up to 54 weeks, which is a little over a year. It includes: * A screening period of up to 2 weeks to check if you are eligible to take part. * A 36-week double-blind treatment period, where you will be randomly assigned (like flipping a coin) to receive either the study drug CS060380 or a placebo (an inactive pill that looks like the study drug). Both groups will also receive semaglutide, which is an approved medicine for weight management. Neither you nor your doctor will know which treatment you are receiving. * A 16-week open-label period, where all participants will receive CS060380. The main goal of this study is to see how the study drug affects the amount of fat in the liver, measured by a special MRI scan, and body weight. We will also monitor your overall health and safety throughout the study by checking your vital signs, doing blood and urine tests, and asking about any side effects you might experience. About 120 participants will take part in this study at almost 15 different hospitals across China, with Ruijin Hospital in Shanghai as the main study site.

Participants needed: 120
Trial details
Phase: Phase 2Age: 18-65Biological sex: AllType: InterventionalSponsor: Cascade Pharmaceuticals, IncUpdated: May 20, 2026Locations: 12
Eligibility criteria

Age 18 to 65 years (inclusive), male or female. [+7]

≥2 episodes of hypoglycemia (blood glucose ≤2.8 mmol/L in non-diabetic patients)... [+43]

Status: Recruiting

Trial of CS060380 Tablets for Non-alcoholic Steatohepatitis (NASH)

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 it aims to answer are: * After 12 weeks of administration, what was the percentage change in fat content evaluated by MRI-PDFF compared to the baseline? * What medical problems do participants have when taking CS060380 tablets? Researchers will compare CS060380 tablets to a placebo (a look-alike substance that contains no drug) to see if CS060380 tablets works to treat NASH. Participants will: * Take CS060380 tablets or a placebo every day for 12 weeks * Visit the clinic for checkups and tests at the frequency required by the protocol * Keep a diary of their symptoms and the number of tablets taken

Participants needed: 120
Trial details
Phase: Phase 2Age: 18-70Biological sex: AllType: InterventionalSponsor: Cascade Pharmaceuticals, IncUpdated: Mar 13, 2026Locations: 8
Eligibility criteria

Men or women aged 18 to 70 (including the boundary value). [+6]

Patients with other clinically significant acute or chronic liver diseases or bi... [+41]

Status: Recruiting

A Study of CS0159 in Patients With PBC With Inadequate Response or Intolerance to UDCA

A Randomized, Double-Blind, Placebo-controlled, Phase III Study to Evaluate the Efficacy and Safety of CS0159 in Patients with Primary Biliary Cholangitis (PBC) with inadequate response or intolerance to ursodeoxycholic acid (UDCA).

Participants needed: 135
Trial details
Phase: Phase 3Age: 18-75Biological sex: AllType: InterventionalSponsor: Cascade Pharmaceuticals, IncUpdated: Dec 30, 2025Locations: 41
Eligibility criteria

Must have given written informed consent (signed and dated) and any authorizatio... [+17]

Previous exposure to CS0159; [+34]