dc.contributor.author
Ratziu, Vlad
dc.contributor.author
Sanyal, Arun
dc.contributor.author
Harrison, Stephen A.
dc.contributor.author
Wong, Vincent Wai‐Sun
dc.contributor.author
Francque, Sven
dc.contributor.author
Goodman, Zachary
dc.contributor.author
Aithal, Guruprasad P.
dc.contributor.author
Kowdley, Kris V.
dc.contributor.author
Seyedkazemi, Star
dc.contributor.author
Fischer, Laurent
dc.contributor.author
Loomba, Rohit
dc.contributor.author
Abdelmalek, Manal F.
dc.contributor.author
Tacke, Frank
dc.date.accessioned
2022-02-16T13:06:17Z
dc.date.available
2022-02-16T13:06:17Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/34025
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-33743
dc.description.abstract
Background and Aims:
Cenicriviroc (CVC) is a C-C chemokine receptors type 2 and 5 dual antagonist under evaluation for treating liver fibrosis in adults with nonalcoholic steatohepatitis (NASH). Year 1 primary analysis of the 2-year CENTAUR study showed that CVC had an antifibrotic effect without impacting steatohepatitis. Herein, we report the final data from year 2 exploratory analyses.
Approach and Results:
This was a randomized, controlled study of adults with NASH, nonalcoholic fatty liver disease activity score ≥4, and NASH Clinical Research Network stage 1-3 fibrosis. Participants in arms A and C received CVC 150 mg or placebo, respectively, for 2 years; arm B received placebo in year 1 and switched to CVC in year 2. Liver biopsy was performed at baseline, year 1, and year 2. Of 289 randomized participants, 242 entered year 2. At year 2, 24% of patients who switched to CVC and 17% who remained on placebo achieved ≥1-stage fibrosis improvement and no worsening of NASH (P = 0.37). Twice the proportion on CVC who achieved fibrosis response at year 1 maintained benefit at year 2 (60% arm A versus 30% arm C), including 86% on CVC who had stage 3 fibrosis at baseline. Over 2 years, a similar proportion on CVC or placebo achieved ≥1-stage fibrosis improvement and no worsening of NASH (15% arm A versus 17% arm C). In patients with fibrosis responses, we observed consistent reductions in levels of N-terminal type 3 collagen propeptide and enhanced liver fibrosis scores, while increases in aspartate aminotransferase-to-platelet ratio index and Fibrosis-4 scores were consistently observed in nonresponders. Safety profile was comparable across groups.
Conclusions:
CVC was well tolerated, and year 2 data corroborate antifibrotic findings from year 1. The majority on CVC who achieved fibrosis response at year 1 maintained it at year 2, with greater effect in advanced fibrosis. ClinicalTrials.gov number, NCT02217475 (CENTAUR).
en
dc.rights.uri
https://creativecommons.org/licenses/by-nc/4.0/
dc.subject
CCR5 Receptor Antagonists
en
dc.subject
Non-alcoholic Fatty Liver Disease
en
dc.subject
Receptors, CCR2
en
dc.subject
Treatment Outcome
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
Cenicriviroc Treatment for Adults With Nonalcoholic Steatohepatitis and Fibrosis: Final Analysis of the Phase 2b CENTAUR Study
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.doi
10.1002/hep.31108
dcterms.bibliographicCitation.journaltitle
Hepatology
dcterms.bibliographicCitation.number
3
dcterms.bibliographicCitation.originalpublishername
Wiley
dcterms.bibliographicCitation.pagestart
892
dcterms.bibliographicCitation.pageend
905
dcterms.bibliographicCitation.volume
72
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.funding
DEAL Wiley
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
31943293
dcterms.isPartOf.issn
0270-9139
dcterms.isPartOf.eissn
1527-3350