Open Label Study to Assess the Predictability of Early Response to Certolizumab Pegol in Patients With Rheumatoid Arthritis

PHASE4CompletedINTERVENTIONAL
Enrollment

132

Participants

Timeline

Start Date

December 31, 2011

Primary Completion Date

May 31, 2015

Study Completion Date

May 31, 2015

Conditions
Rheumatoid Arthritis
Interventions
BIOLOGICAL

Certolizumab pegol

Prefilled syringes containing an injectable volume of 1ml of liquid Certolizumab Pegol (CZP) for single use at a dosage strength of 200 mg/ml. Injections will be given subcutaneously. CZP 400 mg at Week 0, 2 and 4, then continued as maintenance dose of 200 mg every 2 weeks until Week 50.

Trial Locations (18)

Unknown

11, Bari

08, Catania

10, Ferrara

12, Florence

01, Iesi

05, Milan

13, Milan

18, Milan

07, Modena

23, Monserrato

20, Napoli

16, Padua

06, Roma

21, Roma

22, Siena

09, Torino

04, Udine

02, Verona

All Listed Sponsors
lead

UCB Italy s.p.a.

INDUSTRY

NCT01443364 - Open Label Study to Assess the Predictability of Early Response to Certolizumab Pegol in Patients With Rheumatoid Arthritis | Biotech Hunter | Biotech Hunter