Heiner Wedemeyer, E. Gane, Kosh Agarwal, Ömer Fehmi Tabak, Xavier Forns, Ulus Salih Akarca, Viacheslav Morozov, Soo Aleman, Maria Buti, Gurdal Yilmaz, Pietro Lampertico, John Jezorwski, Thomas N. Kakuda, Adam Bakala, Nonko Pehlivanov, Thierry Verbinnen, Oliver Lenz, Michael Biermer
BACKGROUND & AIMS: HDV requires HBsAg for viral assembly. The siRNA JNJ-73763989 (JNJ-3989) targets all HBV transcripts and reduces HBsAg in patients with chronic hepatitis B. We evaluated whether HBsAg reduction with JNJ-3989 leads to a decline in HDV RNA and ALT in patients with chronic hepatitis D (CHD). METHODS: IU/ml reduction of HDV RNA from baseline (or <LLOQ) and normal ALT at treatment week (TW) 48. RESULTS: IU/ml for HDV RNA in active and deferred treatment arms, respectively. Four of five participants in the control arm rolled-over to JNJ-3989 at TW52 including two experiencing subsequent ALT elevations. No ALT elevations were seen in the seven participants with screening HBsAg <10,000 IU/ml. CONCLUSION: This is the first study showing that the HBsAg-targeting siRNA JNJ-3989 can reduce HDV RNA and HBsAg in patients with CHD. Unexpected ALT elevations were seen in 14 of 21 (67%) participants receiving JNJ-3989 (immediate or deferred). GOV IDENTIFIER: NCT04535544 IMPACT AND IMPLICATIONS: In the REEF-D study of patients with chronic hepatitis D, the reduction of HBsAg with the HBsAg-targeting siRNA JNJ-73763989 (JNJ-3989) led to HDV RNA decline, and in some participants, to prolonged HDV RNA suppression. Participants with high HBsAg levels (>10,000 IU/ml) at screening experienced unexpected ALT elevations, sometimes severe, with a return to baseline levels after discontinuation of JNJ-3989. Both HDV RNA reduction and ALT elevation are critical observations for a better understanding of HDV biology and the interplay between viral antigens and the infected hepatocyte. Despite the low sample size and majority of participants not completing the planned treatment course, these findings are important for caregivers and researchers developing novel treatment strategies for patients with chronic hepatitis D.