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Compound · clinical trials

Ursodeoxycholic Acid

Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 6 trials in our China and India registers that name Ursodeoxycholic Acid as an intervention. Synced 24 Sep 2026
6Trials tracked
5Recruiting now
5Lead sponsors
2Country registers
Maintained by Sreepriya Prasannan
MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany HSE Spark Ignite 2026 โ€” Top 14 finalist
Compiled from ClinicalTrials.gov registry records ยท Last verified ยท Editorial standards

Ursodeoxycholic Acid is named as a drug or biological intervention in 6 clinical trials in our China and India trial registers, 5 of which are recruiting. Lead sponsors include Xijing Hospital of Digestive Diseases (2), Institute of Liver and Biliary Sciences, India (1) and Children's Hospital of Fudan University (1). Registered phases: Not applicable, Phase 3, Phase 2 and Phase 4. Conditions studied include Chronic Liver Disease; Biliary Atresia; Cholangitis.

01

Clinical trials of Ursodeoxycholic Acid

6 trials
NCT IDStudyPhaseStatusLead sponsorRegister
NCT06610760 Efficacy and Safety of Ursodeoxycholic Acid in Reversing Gastric Intestinal Metaplasia (ClinicalTrials.gov ↗)
Gastric Intestinal Metaplasia
Phase 4 Recruiting Yongquan Shi China
NCT05751967 Fenofibrate Combined With Ursodeoxycholic Acid in Subjects With Primary Biliary Cholangitis (ClinicalTrials.gov ↗)
Primary Biliary Cholangitis
Phase 3 Recruiting Xijing Hospital of Digestive Diseases China
NCT06755541 Fenofibrate in Combination With Ursodeoxycholic Acid in Primary Biliary Cholangitis: a Real World Study (ClinicalTrials.gov ↗)
Primary Biliary Cholangitis (PBC)
Phase 3 Recruiting Xijing Hospital of Digestive Diseases China
NCT07717242 Sun Yat-Sen Treatment Strategy for Enhancing Response in Muscle-invasive Bladder Cancer (ClinicalTrials.gov ↗)
Bladder Urothelial Carcinoma, Bladder Cancer
Phase 2 Recruiting Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University China
NCT05925309 Preventive Effect of Prophylactic Oral Antibiotics Against Cholangitis After Kasai Portoenterostomy (ClinicalTrials.gov ↗)
Biliary Atresia, Cholangitis, Anti-Bacterial Agents
Not applicable Recruiting Children's Hospital of Fudan University China
NCT07664020 Effect of Ursodeoxycholic Acid Supplementation on Liver Regeneration in Adult Living Donor Liver Transplant (LDLT) Recipients. (ClinicalTrials.gov ↗)
Chronic Liver Disease
Not applicable Not yet open Institute of Liver and Biliary Sciences, India India

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Trial titles and statuses are copied from the registry as published.

02

Conditions studied

9 conditions
Condition (as registered)Trials
Chronic Liver Disease1
Biliary Atresia1
Cholangitis1
Anti-Bacterial Agents1
Bladder Urothelial Carcinoma1
Bladder Cancer1
Gastric Intestinal Metaplasia1
Primary Biliary Cholangitis (PBC)1
Primary Biliary Cholangitis1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
Xijing Hospital of Digestive Diseases2
Institute of Liver and Biliary Sciences, India1
Children's Hospital of Fudan University1
Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University1
Yongquan Shi1
04

Trials by country register

RegisterUrsodeoxycholic Acid trials
Clinical trials in China5
Clinical trials in India1

A trial with sites in more than one country appears in each of those registers.

How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records โ€” it is not written from memory, and nothing here describes how Ursodeoxycholic Acid works or whether it is effective. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists Ursodeoxycholic Acid (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The ClinicalTrials.gov data on this page was last retrieved on 24 Sep 2026.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician โ€” our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us โ€” we correct promptly and log it.