Publication: JNJ-56136379, an HBV Capsid Assembly Modulator, Is Well-Tolerated and Has Antiviral Activity in a Phase 1 Study of Patients With Chronic Infection.
dc.contributor.author | Zoulim, Fabien | |
dc.contributor.author | Lenz, Oliver | |
dc.contributor.author | Vandenbossche, Joris J | |
dc.contributor.author | Talloen, Willem | |
dc.contributor.author | Verbinnen, Thierry | |
dc.contributor.author | Moscalu, Iurie | |
dc.contributor.author | Streinu-Cercel, Adrian | |
dc.contributor.author | Bourgeois, Stefan | |
dc.contributor.author | Buti, Maria | |
dc.contributor.author | Crespo, Javier | |
dc.contributor.author | Manuel Pascasio, Juan | |
dc.contributor.author | Sarrazin, Christoph | |
dc.contributor.author | Vanwolleghem, Thomas | |
dc.contributor.author | Shukla, Umesh | |
dc.contributor.author | Fry, John | |
dc.contributor.author | Yogaratnam, Jeysen Z | |
dc.date.accessioned | 2023-02-08T14:47:37Z | |
dc.date.available | 2023-02-08T14:47:37Z | |
dc.date.issued | 2020-04-25 | |
dc.description.abstract | JNJ-56136379 (JNJ-6379), a capsid assembly modulator that blocks hepatitis B virus (HBV) replication, was well tolerated and demonstrated dose-proportional pharmacokinetics in healthy participants in part 1 of its first clinical trial. In part 2, we have evaluated the safety, pharmacokinetics, and antiviral activity of multiple doses of JNJ-6379 in patients with chronic HBV infection. We performed a double-blind study of 57 treatment-naïve patients with HB e antigen-positive or -negative (74%) chronic HBV infection without cirrhosis. Patients were randomly assigned to groups given JNJ-6379 at 25 mg (100 mg loading dose), 75 mg, 150 mg, or 250 mg or placebo daily for 4 weeks with an 8-week follow-up period. Twenty-three (56%) of 41 patients given JNJ-6379 had at least 1 adverse event (AE) during treatment, compared with 10 (63%) of 16 patients given placebo. No serious AEs were reported during the treatment period. Three patients (7%) given JNJ-6379 vs none given placebo had grade 3 AEs; of these, 1 patient (150 mg) also had an isolated grade 4 increase in the level of alanine aminotransferase that led to treatment discontinuation. JNJ-6379 exposure increased with dose, with time-linear pharmacokinetics. HBV-DNA and HBV-RNA decreased from baseline in patients receiving all doses of JNJ-6379, independently of viral genotype and HB e antigen status. On day 29, 13 (32%) of 41 patients had levels of HBV DNA below the lower limit of quantification. No clinically significant changes in levels of HB surface antigen were observed. In a phase 1 study of treatment-naïve patients with chronic HBV infection, all doses tested of JNJ-6379 were well tolerated, showed dose-dependent pharmacokinetics, and had potent antiviral activity in patients with CHB. The findings support a phase 2a study to evaluate JNJ-6379 ± nucleos(t)ide analogs in patients with chronic HBV infection, which is under way. ClinicalTrials.gov identifier: NCT02662712. | |
dc.identifier.doi | 10.1053/j.gastro.2020.04.036 | |
dc.identifier.essn | 1528-0012 | |
dc.identifier.pmid | 32343960 | |
dc.identifier.unpaywallURL | http://www.gastrojournal.org/article/S0016508520305199/pdf | |
dc.identifier.uri | http://hdl.handle.net/10668/15451 | |
dc.issue.number | 2 | |
dc.journal.title | Gastroenterology | |
dc.journal.titleabbreviation | Gastroenterology | |
dc.language.iso | en | |
dc.organization | Hospital Universitario Virgen del Rocío | |
dc.page.number | 521-533.e9 | |
dc.pubmedtype | Clinical Trial, Phase I | |
dc.pubmedtype | Journal Article | |
dc.pubmedtype | Research Support, Non-U.S. Gov't | |
dc.rights.accessRights | open access | |
dc.subject | Drug | |
dc.subject | HBeAg | |
dc.subject | HBsAg | |
dc.subject | Liver | |
dc.subject.mesh | Administration, Oral | |
dc.subject.mesh | Antiviral Agents | |
dc.subject.mesh | Capsid | |
dc.subject.mesh | DNA, Viral | |
dc.subject.mesh | Dose-Response Relationship, Drug | |
dc.subject.mesh | Double-Blind Method | |
dc.subject.mesh | Female | |
dc.subject.mesh | Hepatitis B virus | |
dc.subject.mesh | Hepatitis B, Chronic | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Male | |
dc.subject.mesh | Middle Aged | |
dc.subject.mesh | Organic Chemicals | |
dc.subject.mesh | Treatment Outcome | |
dc.subject.mesh | Virus Assembly | |
dc.subject.mesh | Young Adult | |
dc.title | JNJ-56136379, an HBV Capsid Assembly Modulator, Is Well-Tolerated and Has Antiviral Activity in a Phase 1 Study of Patients With Chronic Infection. | |
dc.type | research article | |
dc.type.hasVersion | VoR | |
dc.volume.number | 159 | |
dspace.entity.type | Publication |