NCT00799877
Brief summary
The purpose of this study is to evaluate the long-term safety of an Active Drug in Adult Patients with Chronic Plaque Psoriasis (Ps).
Observational study
Age:
From 18 Years to 99 Years.
Inclusion Criteria:
1. An adult patient (18 years of age or older) with chronic plaque psoriasis who has been
prescribed HUMIRA® therapy according to the local product labeling and meets one of
the following criteria:
- New initiated (within 4 weeks of registry entry) on HUMIRA® therapy;
- Initiated HUMIRA® therapy in the past and:
- Has received continuous (no more than 70 consecutive days off drug) HUMIRA®
therapy and the physician can provide source documentation of SAEs, AEs, of
Special Interest, and dosing information since initiation of therapy.
OR
- Is entering after participation in an AbbVie HUMIRA (adalimumab) sponsored study
and has received continuous (no more than 70 consecutive days off drug) HUMIRA®
therapy after the completion of AbbVie sponsored study and physician can provide
source documentation of SAEs, AEs of Special Interest, and dosing information
since initiation of commercial HUMIRA® (defined as a prescribed/non study drug).
2. Patient is willing to consent to data being collected and provided to AbbVie;
3. Patient is capable of and willing to give written informed consent and to comply with
the requirements of the registry.
Exclusion Criteria:
- Patient should not be enrolled if he/she cannot be treated in accordance with the local
product label.