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Article: 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
Title | 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 |
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Authors | |
Issue Date | 1-Apr-2022 |
Publisher | SAGE Publications |
Citation | Antiviral Therapy, 2022, v. 27, n. 3 How to Cite? |
Abstract | Background JNJ-73763989 comprises two hepatitis B virus (HBV)-specific, liver-targeted N-galactosamine-conjugated short interfering RNA triggers, JNJ-73763976 and JNJ-73763924. JNJ-73763989 pharmacokinetics, safety and tolerability were assessed in two phase 1 studies: Japanese (NCT04002752), and non-Japanese healthy participants and chronic hepatitis B (CHB) patients also receiving the HBV capsid assembly modulator JNJ-56136379 and a nucleos(t)ide analogue (NA) (NCT03365947). Methods Healthy participant cohorts were double-blind and randomized to receive a single subcutaneous JNJ-73763989 dose (non-Japanese participants, 35, 100, 200, 300 or 400 mg; Japanese participants, 25, 100 or 200 mg) or placebo. JNJ-73763976 and JNJ-73763924 plasma concentrations were assessed over 48 h. CHB patients received JNJ-73763989 200 mg every 4 weeks plus daily oral JNJ-56136379 250 mg and NA in an open-label fashion. Safety and tolerability were assessed through Day 28 (healthy participants) or Day 112 (patients). Results Thirty non-Japanese (n = 4/dose; placebo, n = 10) and 24 Japanese healthy participants (n = 6/dose; placebo, n = 6) were randomized. JNJ-73763976 and JNJ-73763924 exposure generally increased in a dose-proportional manner. Mean plasma half-life was 4-9 h. No differences between pharmacokinetic parameters were apparent between non-Japanese and Japanese healthy participants. In the 12 CHB patients, mean JNJ-73763976, JNJ-73763924 and JNJ-56136379 plasma concentrations 2 h post-dose on Day 29 were 663, 269 and 14,718 ng/mL, respectively. In both studies, all adverse events were mild/moderate. Conclusion JNJ-73763976 and JNJ-73763924 had short plasma half-lives and exposure generally increased in a dose-proportional manner; there were no pharmacokinetic differences between Japanese and non-Japanese healthy adults. JNJ-73763989 with or without JNJ-56136379 and NA was generally safe and well tolerated. |
Persistent Identifier | http://hdl.handle.net/10722/340810 |
ISSN | 2023 Impact Factor: 1.3 2023 SCImago Journal Rankings: 0.447 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Gane, E | - |
dc.contributor.author | Yuen, MF | - |
dc.contributor.author | Kakuda, TN | - |
dc.contributor.author | Ogawa, T | - |
dc.contributor.author | Takahashi, Y | - |
dc.contributor.author | Goeyvaerts, N | - |
dc.contributor.author | Lonjon-Domanec, I | - |
dc.contributor.author | Vaughan, T | - |
dc.contributor.author | Schluep, T | - |
dc.contributor.author | Hamilton, J | - |
dc.contributor.author | Ediage, EN | - |
dc.contributor.author | Hillewaert, V | - |
dc.contributor.author | Snoeys, J | - |
dc.contributor.author | Lenz, O | - |
dc.contributor.author | Talloen, W | - |
dc.contributor.author | Biermer, M | - |
dc.date.accessioned | 2024-03-11T10:47:26Z | - |
dc.date.available | 2024-03-11T10:47:26Z | - |
dc.date.issued | 2022-04-01 | - |
dc.identifier.citation | Antiviral Therapy, 2022, v. 27, n. 3 | - |
dc.identifier.issn | 1359-6535 | - |
dc.identifier.uri | http://hdl.handle.net/10722/340810 | - |
dc.description.abstract | <p>Background JNJ-73763989 comprises two hepatitis B virus (HBV)-specific, liver-targeted N-galactosamine-conjugated short interfering RNA triggers, JNJ-73763976 and JNJ-73763924. JNJ-73763989 pharmacokinetics, safety and tolerability were assessed in two phase 1 studies: Japanese (NCT04002752), and non-Japanese healthy participants and chronic hepatitis B (CHB) patients also receiving the HBV capsid assembly modulator JNJ-56136379 and a nucleos(t)ide analogue (NA) (NCT03365947). <br></p><p>Methods Healthy participant cohorts were double-blind and randomized to receive a single subcutaneous JNJ-73763989 dose (non-Japanese participants, 35, 100, 200, 300 or 400 mg; Japanese participants, 25, 100 or 200 mg) or placebo. JNJ-73763976 and JNJ-73763924 plasma concentrations were assessed over 48 h. CHB patients received JNJ-73763989 200 mg every 4 weeks plus daily oral JNJ-56136379 250 mg and NA in an open-label fashion. Safety and tolerability were assessed through Day 28 (healthy participants) or Day 112 (patients). <br></p><p>Results Thirty non-Japanese (n = 4/dose; placebo, n = 10) and 24 Japanese healthy participants (n = 6/dose; placebo, n = 6) were randomized. JNJ-73763976 and JNJ-73763924 exposure generally increased in a dose-proportional manner. Mean plasma half-life was 4-9 h. No differences between pharmacokinetic parameters were apparent between non-Japanese and Japanese healthy participants. In the 12 CHB patients, mean JNJ-73763976, JNJ-73763924 and JNJ-56136379 plasma concentrations 2 h post-dose on Day 29 were 663, 269 and 14,718 ng/mL, respectively. In both studies, all adverse events were mild/moderate. <br></p><p>Conclusion JNJ-73763976 and JNJ-73763924 had short plasma half-lives and exposure generally increased in a dose-proportional manner; there were no pharmacokinetic differences between Japanese and non-Japanese healthy adults. JNJ-73763989 with or without JNJ-56136379 and NA was generally safe and well tolerated.</p> | - |
dc.language | eng | - |
dc.publisher | SAGE Publications | - |
dc.relation.ispartof | Antiviral Therapy | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.title | 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 | - |
dc.type | Article | - |
dc.identifier.doi | 10.1177/13596535221093856 | - |
dc.identifier.pmid | 35695169 | - |
dc.identifier.scopus | eid_2-s2.0-85131814421 | - |
dc.identifier.volume | 27 | - |
dc.identifier.issue | 3 | - |
dc.identifier.eissn | 2040-2058 | - |
dc.identifier.isi | WOS:000805019300001 | - |
dc.publisher.place | LONDON | - |
dc.identifier.issnl | 1359-6535 | - |