Seladelpar
DrugCapsule administered orally
NCT Number: NCT07841977
The goal of this clinical study is to learn more about the combination of study drugs seladelpar and cilofexor. The study will assess, the safety, tolerability, and effectiveness of the combination drugs versus both seladelpar alone and placebo, in participants with primary biliary cholangitis (PBC).
The primary objective of this study is to determine whether the combination of seladelpar + cilofexor leads to greater alkaline phosphatase (ALP) reduction than seladelpar alone and describe the safety and tolerability of seladelpar + cilofexor.
Trial opening soon.
Get Notified18 year–75 year
All sexes
Interventional
Phase 2
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Key Inclusion Criteria:
Key Exclusion Criteria:
Note: Other protocol defined Inclusion/Exclusion criteria may apply.
Capsule administered orally
Capsule administered orally
Tablet administered orally
Tablet administered orally
Tablet administered orally
Tablet administered orally
Time frame: Baseline, Week 24
Time frame: First dose up to 30 days post last dose (up to 318 weeks)
Time frame: First dose up to 30 days post last dose (up to 318 weeks)
Time frame: Week 24
Defined as the percentage of participants with ALP < 1.67 × upper limit of normal (ULN), ALP decrease of ≥ 15%, and total bilirubin ≤ 1 × ULN.
Time frame: Week 24
ALP Normalization is defined as ALP ≤ 1.0 × ULN.
Time frame: Baseline, Week 24
Trial opening soon.
Get NotifiedGilead Sciences
Industry
A Phase 2 Proof-of-Concept Study With a Randomized, Double-Blind, Placebo-Controlled Period, Followed by an Active Treatment Extension Period to Assess the Safety and Efficacy of Seladelpar and Cilofexor in Combination for Primary Biliary Cholangitis
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07795151
Bile Duct Diseases, Biliary Tract Diseases
Beijing, Beijing Municipality, China
View Trial DetailsNCT07319169
Bile Duct Diseases, Biliary Tract Diseases
Brussels, Belgium
View Trial DetailsNCT06733519
Bile Duct Diseases, Biliary Tract Diseases
View Trial DetailsNCT07122206
Bile Duct Diseases, Biliary Tract Diseases
View Trial Details