Safety, pharmacokinetics and pharmacodynamics of selgantolimod, an oral Toll-like receptor 8 agonist: a Phase Ia study in healthy subjects.


Journal

Antiviral therapy
ISSN: 2040-2058
Titre abrégé: Antivir Ther
Pays: England
ID NLM: 9815705

Informations de publication

Date de publication:
2020
Historique:
accepted: 04 05 2020
pubmed: 16 7 2020
medline: 7 10 2021
entrez: 16 7 2020
Statut: ppublish

Résumé

Selgantolimod is a novel oral, selective Toll-like receptor 8 (TLR8) agonist in development for the treatment of chronic hepatitis B (CHB). TLR8 is an endosomal innate immune receptor and a target for treatment of viral infections. This first-in-human study investigated the safety, tolerability, pharmacokinetics (PK) and pharmacodynamics (PD) of selgantolimod in healthy volunteers. Of 71 subjects enrolled, 59 received a single dose of selgantolimod (0.5, 1.5, 3 or 5 mg) or placebo, and 12 were evaluated for food effect. Safety, PK and PD activity by induction of cytokines, chemokines and acute phase proteins were assessed. PK/PD analyses were conducted. Single doses of 0.5-5 mg were generally safe. No serious adverse events (AEs) or AEs leading to discontinuation were reported, and most were Grade 1 in severity. Selgantolimod displayed rapid absorption and dose-proportional PK and PD activity. Food had minimal effect on PK but resulted in diminished PD activity. In PK/PD analyses, near-saturation of induction for most evaluated biomarkers occurred at the 5-mg dose. Single doses of up to 5 mg selgantolimod were safe and induced dose-dependent PD responses. These data support evaluation of selgantolimod in combination with other agents in future clinical studies of CHB. Australian New Zealand Clinical Trials Registration: ACTRN12616001646437.

Sections du résumé

BACKGROUND
Selgantolimod is a novel oral, selective Toll-like receptor 8 (TLR8) agonist in development for the treatment of chronic hepatitis B (CHB). TLR8 is an endosomal innate immune receptor and a target for treatment of viral infections. This first-in-human study investigated the safety, tolerability, pharmacokinetics (PK) and pharmacodynamics (PD) of selgantolimod in healthy volunteers.
METHODS
Of 71 subjects enrolled, 59 received a single dose of selgantolimod (0.5, 1.5, 3 or 5 mg) or placebo, and 12 were evaluated for food effect. Safety, PK and PD activity by induction of cytokines, chemokines and acute phase proteins were assessed. PK/PD analyses were conducted.
RESULTS
Single doses of 0.5-5 mg were generally safe. No serious adverse events (AEs) or AEs leading to discontinuation were reported, and most were Grade 1 in severity. Selgantolimod displayed rapid absorption and dose-proportional PK and PD activity. Food had minimal effect on PK but resulted in diminished PD activity. In PK/PD analyses, near-saturation of induction for most evaluated biomarkers occurred at the 5-mg dose.
CONCLUSIONS
Single doses of up to 5 mg selgantolimod were safe and induced dose-dependent PD responses. These data support evaluation of selgantolimod in combination with other agents in future clinical studies of CHB. Australian New Zealand Clinical Trials Registration: ACTRN12616001646437.

Identifiants

pubmed: 32667286
doi: 10.3851/IMP3363
doi:

Substances chimiques

Antiviral Agents 0
Chemokines 0
Hexanols 0
Interleukin 1 Receptor Antagonist Protein 0
Pyrimidines 0
TLR8 protein, human 0
Toll-Like Receptor 8 0
Interleukin-12 187348-17-0
selgantolimod RM4GJT3SMQ

Types de publication

Clinical Trial, Phase I Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

171-180

Auteurs

Maribel Reyes (M)

Clinical Pharmacology, Gilead Sciences, Foster City, CA, USA.

Justin D Lutz (JD)

Clinical Pharmacology, Gilead Sciences, Foster City, CA, USA.

Audrey H Lau (AH)

Clinical Research, Gilead Sciences, Foster City, CA, USA.

Anuj Gaggar (A)

Clinical Research, Gilead Sciences, Foster City, CA, USA.

Ethan P Grant (EP)

Biology, Gilead Sciences, Foster City, CA, USA.

Adarsh Joshi (A)

Biostatistics, Gilead Sciences, Foster City, CA, USA.

Richard L Mackman (RL)

Medicinal Chemistry, Gilead Sciences, Foster City, CA, USA.

John Ling (J)

Bioanalytical Chemistry, Gilead Sciences, Foster City, CA, USA.

Susanna K Tan (SK)

Clinical Research, Gilead Sciences, Foster City, CA, USA.

Natarajan Ayithan (N)

Institute of Human Virology, University of Maryland, Baltimore, MD, USA.

Stephane Daffis (S)

Biology, Gilead Sciences, Foster City, CA, USA.

Jacky Woo (J)

Biology, Gilead Sciences, Foster City, CA, USA.

Peiwen Wu (P)

Biostatistics, Gilead Sciences, Foster City, CA, USA.

Tina Lam (T)

Clinical Operations, Gilead Sciences, Foster City, CA, USA.

Simon P Fletcher (SP)

Biology, Gilead Sciences, Foster City, CA, USA.

Shyamasundaran Kottilil (S)

Institute of Human Virology, University of Maryland, Baltimore, MD, USA.

Bhawna Poonia (B)

Institute of Human Virology, University of Maryland, Baltimore, MD, USA.

Edward J Gane (EJ)

Auckland Clinical Studies, Auckland, New Zealand.

Anita Mathias (A)

Clinical Pharmacology, Gilead Sciences, Foster City, CA, USA.

Polina German (P)

Clinical Pharmacology, Gilead Sciences, Foster City, CA, USA.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH