Overview

Study to Determine if AZD0284 is Effective and Safe in Treating Plaque Psoriasis

Status:
Terminated
Trial end date:
2018-04-18
Target enrollment:
0
Participant gender:
All
Summary
The Sponsor is developing the study drug, AZD0284, for the potential treatment of Plaque psoriasis. Psoriasis is a skin condition that causes red, flaky, crusty patches of skin covered with silvery scales. The severity of the disease varies, but in many cases it can have a major impact on their quality of life if not adequately treated. The purpose of the study is to determine the short term safety, pharmacodynamic and clinical effect of AZD0284 in patients with psoriasis.
Phase:
Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
AstraZeneca
Treatments:
Pharmaceutical Solutions
Criteria
Inclusion Criteria:

- Provision of signed informed consent prior to any study specific procedures.

- At least 6 months documented history with a diagnosis of moderate to severe plaque
psoriasis as defined by the Psoriasis Area and Severity Index (PASI), psoriasis Body
Surface Area (BSA) and static Physician Global Assessment (sPGA).

Exclusion Criteria:

- History of any clinically significant disease or disorder which, in the opinion of the
Investigator, may either put the patient at risk because of participation in the
study, or influence the results or the patient's ability to participate in the study.

- History and/or presence of tuberculosis, hepatitis, HIV. Other opportunistic
infections within 6 months of the study.

- Clinically significant laboratory abnormalities.

- Clinically important abnormalities in rhythm, conduction or morphology of the digital
Electrocardiogram (ECG) as considered by the Investigator may interfere with the
interpretation of study data.

- Current treatment or treatment for psoriasis with biological therapies within 6 months
of study.

- Efficacy and safety failure of biologic therapies targeting the IL-17 and IL12/23
pathway at any time.

- Current treatment or history of treatment for psoriasis with non-biological systemic
medications within 4 weeks of Day 1