An Observational Study to Assess Patient Satisfaction and Control of Psoriasis With Calcipotriene/Betamethasone Dipropionate (Taclonex®) Topical Suspension, and Effect on Quality of Life

Inclusion Criteria:

1. Signed and dated informed consent obtained prior to any study related activities

2. Aged 18 years or above

3. Either sex

4. Any race or ethnicity

5. Attending a hospital outpatient clinic or the private practice of a board-certified
dermatologist, dermatology-certified nurse practitioner or physician assistant
trained in dermatology

6. Clinical diagnosis of psoriasis vulgaris involving scalp and/or body amenable to
treatment with a maximum of 100 g of topical medication per week.

7. Patients who receive a prescription of calcipotriene/betamethasone dipropionate
(Taclonex®) topical suspension 0.005% / 0.064% as per an investigator's clinical
judgment and in accordance with the US label, and who have access to the medication

8. Able to communicate with the investigator, read and understand English, and
understand and comply with the requirements of the study

Exclusion Criteria:

1. Prior treatment with calcipotriene/betamethasone dipropionate (Taclonex®) topical
suspension, 0.005%/0.064%.

2. Contraindications or any warnings/precautions according to the US label.

3. Current participation in any other interventional clinical study.

4. Females who are pregnant, breast-feeding, or females of child-bearing potential
wishing to become pregnant during the study.