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Safety, Pharmacokinetics, and Pharmacodynamics of the Oral TLR8 Agonist Selgantolimod in Chronic Hepatitis B
Author(s) -
Gane Edward J.,
Kim Hyung Joon,
Visvanathan Kumar,
Kim Yoon Jun,
Nguyen AnhHoa,
Wallin Jeffrey J.,
Chen Diana Y.,
McDonald Circe,
Arora Priyanka,
Tan Susanna K.,
Gaggar Anuj,
Roberts Stuart K.,
Lim YoungSuk
Publication year - 2021
Publication title -
hepatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.488
H-Index - 361
eISSN - 1527-3350
pISSN - 0270-9139
DOI - 10.1002/hep.31795
Subject(s) - medicine , pharmacodynamics , pharmacokinetics , dosing , agonist , adverse effect , placebo , clinical endpoint , nausea , immunology , cytokine , gastroenterology , pharmacology , receptor , clinical trial , pathology , alternative medicine
Background and Aims In patients with chronic hepatitis B (CHB) infection, activation of toll‐like receptor 8 may induce antiviral immunity and drive functional cure. Selgantolimod, a toll‐like receptor 8 agonist, was evaluated in patients with CHB who were virally suppressed on oral antiviral treatment or viremic and not on oral antiviral treatment. Approach and Results In this phase 1b study, patients were randomized 4:1 to receive either selgantolimod or placebo once weekly. Virally suppressed patients received either 1.5 mg (for 2 weeks) or 3 mg (for 2 weeks or 4 weeks). Viremic patients received 3 mg for 2 weeks. The primary endpoint was safety, as assessed by adverse events (AEs), laboratory abnormalities, and vital sign examination. Pharmacokinetic and pharmacodynamic parameters were assessed by plasma analysis. A total of 38 patients (28 virally suppressed, 10 viremic) were enrolled from six sites in Australia, New Zealand, and South Korea. Twenty patients (53%) experienced an AE and 32 (84%) had laboratory abnormalities, all of which were mild or moderate in severity. The most common AEs were headache (32%), nausea (24%), and dizziness (13%). With a half‐life of 5 hours, no accumulation of selgantolimod was observed with multiple dosing. Selgantolimod induced transient dose‐dependent increases in serum cytokines, including IL‐12p40 and IL‐1RA, which are important for the expansion and activity of multiple T‐ cell subsets and innate immunity. Conclusion Selgantolimod was safe and well‐tolerated in virally suppressed and viremic patients with CHB and elicited cytokine responses consistent with target engagement. Further studies with longer durations of selgantolimod treatment are required to evaluate efficacy.