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A phase 2 dose-finding study of lonafarnib and ritonavir with or without interferon alpha for chronic delta hepatitis
Hepatology ( IF 13.5 ) Pub Date : 2021-12-03 , DOI: 10.1002/hep.32259
Cihan Yurdaydin 1, 2, 3 , Onur Keskin 1 , Esra Yurdcu 2 , Aysun Çalişkan 1 , Soner Önem 1 , Fatih Karakaya 1 , Çağdaş Kalkan 1 , Ersin Karatayli 2, 4 , Senem Karatayli 2, 4 , Ingrid Choong 5 , David Apelian 5 , Christopher Koh 6 , Theo Heller 6 , Ramazan Idilman 1 , A Mithat Bozdayi 2 , Jeffrey S Glenn 7, 8
Affiliation  

Proof-of-concept studies demonstrated lonafarnib (LNF), a first-in-class oral prenylation inhibitor, efficacy in patients infected with HDV. The lonafarnib with ritonavir for HDV-2 (LOWR-2) study’s aim was to identify optimal combination regimens of LNF + ritonavir (RTV) ± pegylated interferon alpha (PEG-IFNα) with efficacy and tolerability for longer-term dosing. Here we report the safety and efficacy at end of treatment for up to 24 weeks.

中文翻译:

lonafarnib 和利托那韦联合或不联合干扰素 α 治疗慢性 δ 肝炎的 2 期剂量探索研究

概念验证研究表明,lonafarnib (LNF) 是一种一流的口服异戊二烯化抑制剂,对 HDV 感染的患者有效。lonafarnib 与利托那韦用于 HDV-2 (LOWR-2) 研究的目的是确定 LNF + 利托那韦 (RTV) ± 聚乙二醇干扰素 α (PEG-IFNα) 的最佳组合方案,具有长期给药的有效性和耐受性。在这里,我们报告了长达 24 周的治疗结束时的安全性和有效性。
更新日期:2021-12-03
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