Clinical Pharmacokinetics, Safety, and Tolerability of a Novel, First-in-Class TRPV4 Ion Channel Inhibitor, GSK2798745, in Healthy and Heart Failure Subjects.


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
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

Pagination

335-342

Auteurs

Navin Goyal (N)

GlaxoSmithKline, UP4300 East, 1250 S College Road, Collegeville, PA, 19426, USA. navinkumar.s.goyal@gsk.com.

Pete Skrdla (P)

GlaxoSmithKline, UP4300 East, 1250 S College Road, Collegeville, PA, 19426, USA.

Rosemary Schroyer (R)

GlaxoSmithKline, UP4300 East, 1250 S College Road, Collegeville, PA, 19426, USA.

Subramanya Kumar (S)

GlaxoSmithKline Clinical Unit Cambridge, Addenbrooke's Hospital, Cambridge, UK.

Disala Fernando (D)

GlaxoSmithKline Clinical Unit Cambridge, Addenbrooke's Hospital, Cambridge, UK.

Anna Oughton (A)

GlaxoSmithKline, UP4300 East, 1250 S College Road, Collegeville, PA, 19426, USA.

Nicola Norton (N)

GlaxoSmithKline Clinical Unit Cambridge, Addenbrooke's Hospital, Cambridge, UK.

Dennis L Sprecher (DL)

GlaxoSmithKline, UP4300 East, 1250 S College Road, Collegeville, PA, 19426, USA.

Joseph Cheriyan (J)

GlaxoSmithKline Clinical Unit Cambridge, Addenbrooke's Hospital, Cambridge, UK.
Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.

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