A Canadian Open-Label Access Program to Evaluate Adalimumab When Added to Inadequate Therapy for the Treatment of Psoriasis

PHASE3CompletedINTERVENTIONAL
Enrollment

203

Participants

Timeline

Start Date

September 30, 2007

Primary Completion Date

September 30, 2008

Conditions
Psoriasis
Interventions
BIOLOGICAL

Humira (adalimumab)

Study drug will be provided as a sterile, preservative-free solution for subcutaneous injection, contained in a pre-filled syringe housed in a pen device (pre-filled pen). Loading dose of 80 mg of adalimumab subcutaneously (sc) at Baseline, and 40 mg of adalimumab sc at Week 1, followed by 40 mg of adalimumab sc every other week (eow) for 24 weeks.

Trial Locations (27)

T2S 3B3

Calgary

T3A 2N1

Calgary

T5K 1X3

Edmonton

V3R 6A7

Surrey

V5Z 4E8

Vancouver

R3C 0N2

Winnipeg

R3C 1R4

Winnipeg

E1C 8X3

Moncton

A1B 3E1

St. John's

A1C 2H5

St. John's

B3H 1Z4

Halifax

L4M 6L2

Barrie

L0S 1C0

Fenwick

L8N 1V6

Hamilton

N5X 2P1

London

N6A 3H7

London

L3P 1A8

Markham

K2G 6E2

Nepean

P1B 3Z7

North Bay

L6J 7W5

Oakville

L6K 1E1

Oakville

M4V 1R1

Toronto

N2J 1C4

Waterloo

H3Z 2S6

Montreal

G1J 1X7

Québec

J1H 1Z1

Sherbrooke

G1V 4X7

Ste-Foy

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Abbott

INDUSTRY