Safety and Tolerability of NNC0114-0006 at Increasing Dose Levels in Subjects With Rheumatoid Arthritis

PHASE1CompletedINTERVENTIONAL
Enrollment

32

Participants

Timeline

Start Date

March 31, 2012

Primary Completion Date

October 31, 2013

Study Completion Date

October 31, 2013

Conditions
InflammationRheumatoid Arthritis
Interventions
DRUG

NNC0114-0006

Multiple subcutaneous (s.c., under the skin) doses administered every second week for six weeks. The trial comprises dose escalation up to four dose levels. Progression to next dose will be based on safety evaluation.

DRUG

placebo

Multiple subcutaneous (s.c., under the skin) doses administered every second week for six weeks.

Trial Locations (5)

10117

Novo Nordisk Investigational Site, Berlin

117556

Novo Nordisk Investigational Site, Moscow

119435

Novo Nordisk Investigational Site, Moscow

125284

Novo Nordisk Investigational Site, Moscow

150003

Novo Nordisk Investigational Site, Yaroslavl

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Novo Nordisk A/S

INDUSTRY