drugset / Trial / NCT03365947
Study of ARO-HBV in Normal Adult Volunteers and Patients With Hepatitis B Virus (HBV)
RandomizedParallel-groupDouble-blindTreatment
Summary
The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of single- and multiple-ascending doses of ARO-HBV in healthy adult volunteers and participants with hepatitis B virus (HBV).
Timeline
- Start
- 2018-03-27
- Primary completion
- 2020-04-23
- Completion
- 2020-04-23
Publications
- Results Yuen MF, Locarnini S, Lim TH, Strasser SI, Sievert W, Cheng W, Thompson AJ, Given BD, Schluep T, Hamilton J, Biermer M, Kalmeijer R, Beumont M, Lenz O, De Ridder F, Cloherty G, Ka-Ho Wong D, Schwabe C, Jackson K, Lai CL, Gish RG, Gane E. Combination treatments including the small-interfering RNA JNJ-3989 induce rapid and sometimes prolonged viral responses in patients with CHB. J Hepatol. 2022 Nov;77(5):1287-1298. doi: 10.1016/j.jhep.2022.07.010. Epub 2022 Jul 20.
- Gane E, Yuen MF, Kakuda TN, Ogawa T, Takahashi Y, Goeyvaerts N, Lonjon-Domanec I, Vaughan T, Schluep T, Hamilton J, Njumbe Ediage E, Hillewaert V, Snoeys J, Lenz O, Talloen W, Biermer M. JNJ-73763989 pharmacokinetics and safety: Liver-targeted siRNAs against hepatitis B virus, in Japanese and non-Japanese healthy adults, and combined with JNJ-56136379 and a nucleos(t)ide analogue in patients with chronic hepatitis B. Antivir Ther. 2022 Jun;27(3):13596535221093856. doi: 10.1177/13596535221093856.
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | ARO-HBV | Unknown | 25 mg | Subcutaneous |
| Subject | ARO-HBV | Unknown | 35 mg | Subcutaneous |
| Subject | ARO-HBV | Unknown | 50 mg | Subcutaneous |
| Subject | ARO-HBV | Unknown | 100 mg | Subcutaneous |
| Subject | ARO-HBV | Unknown | 200 mg | Subcutaneous |
| Subject | ARO-HBV | Unknown | 300 mg | Subcutaneous |
| Subject | ARO-HBV | Unknown | 400 mg | Subcutaneous |
| Subject | bersacapavir | Other / unclassified | 250 mg | — |