Monitoring the Response of Combination Ursodiol and Seladelpar Treatment

NCT07122206 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2025-08-14

No results posted yet for this study

Summary

This study aims to provide comprehensive insights into the therapeutic effects of combination treatment with ursodiol and seladelpar in PBC patients by assessing biochemical responses using biomarkers such as ALP and total bilirubin.

Conditions

Interventions

PROCEDURE

Blood Draws

Research-related blood draws will be used to ascertain FGF19 levels.

Sponsors & Collaborators

  • Methodist Health System

    lead OTHER

Principal Investigators

  • Mangesh Pagadala, MD · Methodist Heath System

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-08-31
Primary Completion
2027-08-31
Completion
2027-08-31

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07122206 on ClinicalTrials.gov