医学
慢性肝炎
病毒学
病毒
乙型肝炎病毒
干扰素
临床研究阶段
相(物质)
免疫学
肝炎病毒
慢性病
正庚病毒
七鳃鳗科
小干扰RNA
病毒性疾病
慢性肝病
乙型肝炎
丙型肝炎病毒
作者
Patrick Kennedy,S. Fung,Maria Buti,Gürdal Yılmaz,Wan‐Long Chuang,Tarik Asselah,Masayuki Kurosaki,John Jezorwski,Vladislav Klyashtornyy,Thierry Verbinnen,Thomas N. Kakuda,Oliver Lenz,Carine Guinard‐Azadian,Michael Biermer
出处
期刊:Gut
[BMJ]
日期:2025-11-04
卷期号:75 (5): 1043-1054
被引量:2
标识
DOI:10.1136/gutjnl-2025-336592
摘要
Background In the hepatitis B e antigen positive (HBeAg+) chronic infection disease phase, approved treatments have limited effects on hepatitis B surface antigen (HBsAg) and HBeAg. Objective The phase 2 REEF-IT study ( NCT04439539 ) assessed safety, efficacy and pharmacokinetics of pegylated interferon-α2a (PegIFN-α2a) add-on to JNJ-73763989 (JNJ-3989)±bersacapavir+nucleos(t)ide analogues (NA) in not currently treated, HBeAg+chronic hepatitis B. Design Participants received JNJ-3989 (200 mg every 4 weeks)+NA±bersacapavir (250 mg daily) for 36–52 weeks (induction) followed by 12 weeks of PegIFN-α2a (180 µg weekly) add-on. The primary endpoint was the proportion of participants with HBsAg seroclearance 24 weeks after stopping all treatment including NA. Changes in viral markers, safety and pharmacokinetics were assessed. Results 49/54 (91%) enrolled participants completed the study; 52% were male, with mean age of 33.6 years. No participant achieved the primary endpoint; one met NA completion criteria. 11/54 (20.4%) participants achieved HBsAg seroclearance at least once, 6 of them maintained it until Follow-up Week 48 (FUW48). Overall mean (SE) change from baseline in HBsAg of –2.85 (0.13), –3.61 (0.18) and –2.63 (0.26)log 10 IU/mL were observed at end of induction, end of treatment and FUW48. 16/53 (30.2%) participants reached HBeAg seroclearance at least once; 12 maintained it until FUW48. Similar proportions of participants experienced an adverse event (AE) during induction (83.3%), PegIFN-α2a add-on (85.7%) and follow-up (64.7%). There were no deaths or serious AEs; two participants discontinued PegIFN-α2a. Conclusions In this population, adding PegIFN-α2a increased HBsAg declines after reductions by JNJ-3989; 20.4% achieved HBsAg seroclearance at least once. Treatment was generally safe with acceptable tolerability. Trial registration number NCT04439539 .
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