A First in Human Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of a Intravenous (IV) Dose of GSK2831781 in Healthy Volunteers and Patients With Plaque Psoriasis

PHASE1CompletedINTERVENTIONAL
Enrollment

67

Participants

Timeline

Start Date

July 30, 2014

Primary Completion Date

March 7, 2018

Study Completion Date

March 7, 2018

Conditions
Psoriasis
Interventions
BIOLOGICAL

GSK2831781

GSK2831781 (100 milligram (mg)/mL) and its dilutions (Diluent - 0.9 percent saline solution containing 0.015 percent Polysorbate 80) as clear or opalescent, colourless, yellow to brown liquid solution administered by IV over approximately 2 hours.

BIOLOGICAL

Placebo

Commercial saline solution administered by IV over approximately 2 hours

Trial Locations (3)

14050

GSK Investigational Site, Berlin

53127

GSK Investigational Site, Bonn

Unknown

GSK Investigational Site, London

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

Parexel

INDUSTRY

lead

GlaxoSmithKline

INDUSTRY