Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics Investigation of GSK3335065 Intravenous (IV) Infusion in Healthy Adults

PHASE1TerminatedINTERVENTIONAL
Enrollment

18

Participants

Timeline

Start Date

August 22, 2017

Primary Completion Date

May 19, 2018

Study Completion Date

May 19, 2018

Conditions
Pancreatitis, Acute Necrotizing
Interventions
DRUG

GSK3335065

GSK3335065 is being developed as a treatment for acute pancreatitis with the intent of reducing 3-hydroxykynurenine (3HK) levels to the normal range (or lower) and maintaining them at this level. GSK3335065 is a solution and will be administered as intravenous injection and infusion with dose strength of 5 milligram (mg)/mL that may be diluted in 0.9% weight by volume (w/v) sodium chloride.

DRUG

Placebo

Placebo solution to match GSK3335065 will be given as intravenous injection and infusion.

Trial Locations (1)

CB2 0GG

GSK Investigational Site, Cambridge

Sponsors

Lead Sponsor

All Listed Sponsors
lead

GlaxoSmithKline

INDUSTRY