Prospective Registry-Based Study Evaluating the Effectiveness and Safety of Odevixibat in Participants with Alagille Syndrome (ALGS)
Prospective Registry-Based Study Evaluating the Effectiveness and Safety of Odevixibat in Participants with Alagille Syndrome (ALGS)
Sponsor: Ipsen Pharma SAS
Enrolling: Male and Female Patients
IRB Number: AAAV7459
U.S. Govt. ID: NCT06850038
Contact: Transplant Clinical Research Center: 212-305-3839 / tcrcstudyreferral@cumc.columbia.edu
Additional Study Information: This study is evaluating how well odevixibat, an approved medication for Alagille Syndrome (ALGS), works in real-world clinical practice and how safe it is for long-term use. Participants with ALGS who are receiving odevixibat as part of their usual medical care will be followed for about five years. During this time, information from routine clinic visits will be collected to understand how treatment affects liver health, growth, and development, and to identify any side effects. This research may help improve care and future treatment options for people living with ALGS. If you have any questions regarding this study, please contact the Transplant Clinical Research Center (TCRC).
Investigator
Mercedes Martinez, MD
Do You Qualify?
Do you or your child have a diagnosis of Alagille Syndrome (ALGS)? Yes No
Are you or your child currently being treated with or about to start treatment with odevixibat? Yes No
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For more information, please contact:
Transplant Clinical Research Center
tcrcstudyreferral@cumc.columbia.edu
212-305-3839