TerminatedPHASE2, PHASE3NCT06121375
Study to Assess Efficacy, Safety, Tolerability, Pharmacokinetics (PK), and Pharmacodynamics (PD) of Obeticholic Acid (OCA) Compared to Placebo in Pediatric Participants With Biliary Atresia, Post-hepatoportoenterostomy
Studying Isolated biliary atresia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Intercept Pharmaceuticals
- Principal Investigator
- Lynda Szczech, MDIntercept Pharmaceuticals
- Intervention
- OCA(drug)
- Enrollment
- 28 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2024 – 2025
Study locations (24)
- Queensland Childrens Hospital, South Brisbane, Queensland, Australia
- Women's and Children's Hospital, North Adelaide, South Australia, Australia
- Royal Childrens Hospital, Parkville, Victoria, Australia
- Alberta Childrens Hospital, Calgary, Alberta, Canada
- Stollery Children's Hospital, Edmonton, Alberta, Canada
- Children's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China
- Guangzhou Women And Childrens Medical Center, Guangzhou, China
- Children's Hospital of Fudan University, Shanghai, China
- Childrens Hospital of Shanghai, Shanghai, China
- Children's Hospital of Shanxi, Taiyuan, China
- Queen Mary Hospital, Hong Kong, Hong Kong
- Hadassah Medical Center, Jerusalem, Israel
- Shaare-Zedek Medical Center, Jerusalem, Israel
- Hospital Raja Perempuan Azinab II, Kota Bharu, Kelantan, Malaysia
- University Malaya Medical Center, Kuala Lumpur, Malaysia
- +9 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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