Clinical Pharmacokinetics, Safety, and Tolerability of a Novel, First-in-Class TRPV4 Ion Channel Inhibitor, GSK2798745, in Healthy and Heart Failure Subjects.
Administration, Oral
Adult
Aged
Area Under Curve
Benzimidazoles
/ adverse effects
Case-Control Studies
Double-Blind Method
Drug Administration Schedule
Female
Food-Drug Interactions
Half-Life
Heart Failure
/ drug therapy
Humans
Male
Spiro Compounds
/ adverse effects
TRPV Cation Channels
/ antagonists & inhibitors
Journal
American journal of cardiovascular drugs : drugs, devices, and other interventions
ISSN: 1179-187X
Titre abrégé: Am J Cardiovasc Drugs
Pays: New Zealand
ID NLM: 100967755
Informations de publication
Date de publication:
Jun 2019
Jun 2019
Historique:
pubmed:
15
1
2019
medline:
21
12
2019
entrez:
15
1
2019
Statut:
ppublish
Résumé
Pulmonary capillary endothelial transient receptor potential vanilloid 4 (TRPV4) channel plays a critical role in mediating the development of cardiogenic pulmonary edema. GSK2798745 is a first-in-class, highly potent, selective, orally active TRPV4 channel blocker being evaluated in a first-time-in-humans study (NCT02119260). GSK2798745 was administered in a randomized, placebo-controlled study design to healthy volunteers in three separate cohorts as single escalating doses, with and without food, and as once-daily repeat doses for up to 14 days, respectively. Two cohorts of subjects with mild to moderate heart failure were also administered GSK2798745 once daily for up to 7 days. Safety, tolerability, and systemic exposure data were collected. No significant safety issues or serious adverse events were observed with GSK2798745 in healthy volunteers and patients with heart failure. GSK2798745 systemic exposure data demonstrated linear pharmacokinetics up to 12.5 mg, less than twofold accumulation with once-daily dosing, and a systemic half-life of ~ 13 h. There was a slight increase in GSK2798745 exposure [14% increase in area under the plasma concentration-time curve (AUC) and 9% increase in maximum observed plasma concentration (C GSK2798745 was well-tolerated in healthy volunteers and patients with stable heart failure. The safety and exposure data obtained in this study allow further evaluation of the drug in long-term clinical studies in heart failure as well as other indications.
Identifiants
pubmed: 30637626
doi: 10.1007/s40256-018-00320-6
pii: 10.1007/s40256-018-00320-6
doi:
Substances chimiques
Benzimidazoles
0
GSK2798745
0
Spiro Compounds
0
TRPV Cation Channels
0
TRPV4 protein, human
0
Banques de données
ClinicalTrials.gov
['NCT02119260']
Types de publication
Journal Article
Randomized Controlled Trial
Langues
eng
Sous-ensembles de citation
IM