A Study to Evaluate the Safety, Mode of Action and Clinical Efficacy of GSK3050002 in Subjects With Psoriatic Arthritis

PHASE1WithdrawnINTERVENTIONAL
0
Timeline

Start Date

June 1, 2018

Primary Completion Date

August 9, 2019

Study Completion Date

August 9, 2019

Conditions
Autoimmune Diseases
Interventions
DRUG

GSK3050002

The 3 mL glass vial contains white to off-white lyophilized powder which requires reconstitution with sterile water for injection.Prepared as 100 milligrams per milliliter (mg/mL) solution; lower concentrations prepared by dilution with 0.9% weight by volume (w/v) sodium chloride Injection for infusion.

DRUG

Placebo

Normal saline (0.9% sodium chloride) will be used as placebo.

Trial Locations (1)

OX3 7LD

GSK Investigational Site, Oxford

Sponsors

Lead Sponsor

All Listed Sponsors
lead

GlaxoSmithKline

INDUSTRY