The Quality of Life Study in Psoriasis Patients After Ustekinumab Treatment

The primary objective of this study is to demonstrate improvement in psoriasis patient
quality of life after 36 weeks with ustekinumab through the use of validated dermatologic
and non-dermatologic psychometric instruments.

Inclusion Criteria:

1. Subjects are non-immunocompromised males or females 18 years of age or older

2. Subjects have moderate-to-severe (≥10% total body surface area) plaque psoriasis

3. Subject diagnosed at least 6 months prior to entering the study

4. Negative urine pregnancy test within 7 days before the first dose of ustekinumab in
all women (except those surgically sterile or at least 5 years postmenopausal)

5. Sexually active subjects of childbearing potential must agree to use medically
acceptable form of contraception during screening and throughout the study.

6. Are considered eligible according to the following tuberculosis (TB) screening
criteria:

- Have no history of latent or active TB prior to screening. An exception is made
for subjects currently receiving treatment for latent TB with no evidence of
active TB, or who have a history of latent TB and documentation of having
completed appropriate treatment for latent TB within 3 years prior to the first
administration of study agent. It is the responsibility of the investigator to
verify the adequacy of previous antituberculous treatment and provide
appropriate documentation.

- Have no signs or symptoms suggestive of active TB upon medical history and/or
physical examination.

- Have had no recent close contact with a person with active TB or, if there has
been such contact, will be referred to a physician specializing in TB to undergo
additional evaluation and, if warranted, receive appropriate treatment for
latent TB prior to or simultaneously with the first administration of study
agent.

- Within 1 month prior to the first administration of study agent, have a negative
QuantiFERON-TB Gold test result, or have a newly identified positive
QuantiFERON-TB Gold test result in which active TB has been ruled out and for
which appropriate treatment for latent TB has been initiated either prior to or
simultaneously with the first administration of study agent. The QuantiFERON-TB
Gold test are not required at screening for subjects with a history of latent TB
and ongoing treatment for latent TB or documentation of having completed
adequate treatment as described above; Subjects with documentation of having
completed adequate treatment as described above are not required to initiate
additional treatment for latent TB.

- Have a chest radiograph both posterior-anterior and lateral views, taken within
3 months prior to the first administration of study agent and read by a
qualified radiologist, with no evidence of current, active TB or old, inactive
TB.

7. Subject meets concomitant medication requirements or agrees to complete a washout for
restricted medications prior to starting the study.

- Washout Period :

- Must not have initiated or changed any other medications that could affect
psoriasis (e.g. beta blockers, lithium salts, antimalarials) within the 4
week period prior to Week 0 or during the study

- Subjects must not have received immunosuppressive, chemotherapy and/or
systemic therapy including oral calcineurin inhibitors (such as
cyclosporine), retinoids (Vitamin A and analogues), Methotrexate,
Azathioprine, 6-thioguanine, Mycophenolate mofetil (MMF), Hydroxyurea, or
cytokines (such as interferon-gamma) within the 4 week period prior to Week
0 or during the study

- Subjects must not have received phototherapy (broadband or narrow-band UVB)
within the 2 week period prior to Week 0 or during the study.

- Subjects must not have received photochemotherapy (PUVA) within the 4 week
period prior to week 0 or during the study

- Subjects must not have received TNF-α inhibitors (such as infliximab,
etanercept, adalimumab) within the 12 week period prior to Week 0 or during
the study

- Subjects must not have received alefacept within the 12 week period prior
to Week 0 or during the study.

- Subjects must not have received ustekinumab within the 12 week period prior
to Week 0 or during the study.

- Subjects must not have received treatment with an investigational drug
within the previous 4 weeks or 5 half-lives prior to Week 0 (whichever is
longer) or participation in another clinical trial within the 4 week period
prior to Week 0 or during the study

Exclusion Criteria:

1. Subject is younger than 18 years of age.

2. Subject has less than 10% body surface involvement of his/her psoriasis.

3. Subjects with erythrodermic, pustular, or guttate psoriasis

4. History of known or suspected intolerance to any of the ingredients of the
investigational study product.

5. Evidence of skin conditions other than psoriasis that would interfere with
study-related evaluations of psoriasis.

6. Evidence of active infections such as fevers, chills, sweats, or history of untreated
Lyme disease and active severe infections within 4 weeks before screening visit, or
between the screening and Week 0 visits

7. Subject has a history of listeriosis, untreated TB, persistent or active infections
requiring hospitalization or treatment with IV antibiotics, IV antiretrovirals, or IV
antifungals within 30 days of baseline, or oral antibiotics, antivirals, or
antifungals for purpose of treating infection, within 14 days of baseline.

8. Have a history of latent or active granulomatous infection, including histoplasmosis
or coccidioidomycosis, prior to screening.

9. Refer to inclusion criteria for information regarding eligibility with a history of
latent TB.

10. Have had a Bacille Calmette-Guerin (BCG) vaccination within 12 months of screening.

11. Have a chest radiograph within 3 months prior to the first administration of study
agent that shows an abnormality suggestive of malignancy or current active infection,
including TB.

12. Have had a nontuberculous mycobacterial infection or opportunistic infection (eg.
Cytomegalovirus, pneumocystosis, aspergillosis) within 6 months prior to screening.

13. History of immune compromised status [e.g. human immunodeficiency virus (HIV)
positive status or other immune suppressing drug] or a congenital or acquired
immunodeficiency or subject testing positive for HIV, Hepatitis B, and/or Hepatitis C
during screening procedures.

14. Subject has a poorly controlled medical condition including, but not limited to,
unstable cardiovascular disease, poorly controlled diabetes, recent stroke, history
of recurrent infections, or any other condition for which, in the opinion of the
investigator, participation in the study would place the subject at risk

15. Subject has a history of or ongoing drug or alcohol abuse

16. Subject is not willing to comply with wash-out requirements (see above)

17. Subject is known, or suspected of being unable to comply with the study protocol