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ISSN 1001-5256 (Print)
ISSN 2097-3497 (Online)
CN 22-1108/R
Volume 40 Issue 5
May  2024
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Article Contents

Advances in drug therapy for primary sclerosing cholangitis

DOI: 10.12449/JCH240526
Research funding:

National Natural Science Foundation of China (82200666)

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  • Corresponding author: LI Xinyu, xinyuli@jlu.edu.cn (ORCID: 0000-0001-6215-4708); WANG Lihong, whlhebykdx@163.com (ORCID: 0009-0009-6263-0028); NIU Junqi, junqiniu@jlu.edu.cn (ORCID: 0000-0001-5415-2024)
  • Received Date: 2023-08-29
  • Accepted Date: 2023-10-30
  • Published Date: 2024-05-25
  • Primary sclerosing cholangitis (PSC) is a cholestatic disease characterized by chronic progressive bile duct inflammation and has a low incidence rate and poor prognosis in China. There is still no drug therapy that can change the course of PSC, and liver transplantation is the only effective treatment for PSC, with a 5-year survival rate of 85% after transplantation. Drug therapy for PSC is facing great challenges based on the current status of PSC. At present, drugs for the treatment of PSC are in the stage of clinical trials and have shown certain application prospect, among which ursodeoxycholic acid is the most widely studied and commonly used drug. In addition, there are many emerging drugs in the pipeline. This article summarizes the latest advances in drug therapy for PSC.

     

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