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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.authorZoulim, Fabien
dc.contributor.authorLenz, Oliver
dc.contributor.authorVandenbossche, Joris J
dc.contributor.authorTalloen, Willem
dc.contributor.authorVerbinnen, Thierry
dc.contributor.authorMoscalu, Iurie
dc.contributor.authorStreinu-Cercel, Adrian
dc.contributor.authorBourgeois, Stefan
dc.contributor.authorButi, Maria
dc.contributor.authorCrespo, Javier
dc.contributor.authorManuel Pascasio, Juan
dc.contributor.authorSarrazin, Christoph
dc.contributor.authorVanwolleghem, Thomas
dc.contributor.authorShukla, Umesh
dc.contributor.authorFry, John
dc.contributor.authorYogaratnam, Jeysen Z
dc.date.accessioned2023-02-08T14:47:37Z
dc.date.available2023-02-08T14:47:37Z
dc.date.issued2020-04-25
dc.description.abstractJNJ-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.doi10.1053/j.gastro.2020.04.036
dc.identifier.essn1528-0012
dc.identifier.pmid32343960
dc.identifier.unpaywallURLhttp://www.gastrojournal.org/article/S0016508520305199/pdf
dc.identifier.urihttp://hdl.handle.net/10668/15451
dc.issue.number2
dc.journal.titleGastroenterology
dc.journal.titleabbreviationGastroenterology
dc.language.isoen
dc.organizationHospital Universitario Virgen del Rocío
dc.page.number521-533.e9
dc.pubmedtypeClinical Trial, Phase I
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rights.accessRightsopen access
dc.subjectDrug
dc.subjectHBeAg
dc.subjectHBsAg
dc.subjectLiver
dc.subject.meshAdministration, Oral
dc.subject.meshAntiviral Agents
dc.subject.meshCapsid
dc.subject.meshDNA, Viral
dc.subject.meshDose-Response Relationship, Drug
dc.subject.meshDouble-Blind Method
dc.subject.meshFemale
dc.subject.meshHepatitis B virus
dc.subject.meshHepatitis B, Chronic
dc.subject.meshHumans
dc.subject.meshMale
dc.subject.meshMiddle Aged
dc.subject.meshOrganic Chemicals
dc.subject.meshTreatment Outcome
dc.subject.meshVirus Assembly
dc.subject.meshYoung Adult
dc.titleJNJ-56136379, an HBV Capsid Assembly Modulator, Is Well-Tolerated and Has Antiviral Activity in a Phase 1 Study of Patients With Chronic Infection.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number159
dspace.entity.typePublication

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