Study to Assess Change in Disease Symptoms in Adult Participants With Moderate to Severe Psoriasis Treated With Subcutaneous Risankizumab Injection According to Standard of Care

N/AActive Not RecruitingNCT04780516

AbbVie141 enrolled

Overview

Psoriasis is a chronic inflammatory skin condition that is characterized by symptoms such as pain, itching and discomfort. This can have severe impact on the quality of life including depression, embarrassment, and social isolation. The objective of this study is to evaluate how effective risankizumab is in changing the disease symptoms in adult participants with moderate to severe psoriasis. Risankizumab is an approved drug being developed for the treatment of psoriasis. Adult participants who are prescribed risankizumab treatment according to the local label will be enrolled in this study. Approximately 125 adult participants with moderate to severe psoriasis will be enrolled at multiple sites across Israel. Participants who are prescribed to receive subcutaneous risankizumab injection by their physician according to local label will be enrolled and will be followed for approximately 2 years. There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular visits during the study at a hospital or clinic. The effect of the treatment will be checked by medical assessments, checking for side effects, patient charts, questionnaires, and remote monitoring device (patch sensor).

Study Type

OBSERVATIONAL

Enrollment

141

Conditions

Psoriasis

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Clinical diagnosis of moderate to severe psoriasis. * Prescribed risankizumab as the standard treatment for psoriasis, according to the local label. The decision to prescribe risankizumab will be made solely by the physician, based on his clinical judgment, and is done prior to any decision to approach the participant to participate in this study. * Willing to be involved in the study, to sign an informed consent form and complete study questionnaires. * Participants participating in digital component: Pruritus Numeric Rating Scale (PNRS) score \>=4 at baseline. Exclusion Criteria: * Participants participating in a concurrent clinical interventional study or within 30 days. * Participants treated with risankizumab prior to baseline visit.

Locations (11)

Duplicate_Kaplan Medical Center /ID# 226569

Rehovot, Central District, Israel

Leumit /ID# 252029

Rehovot, Central District, Israel

HaEmek Medical Center /ID# 251040

Afula, Haifa District, Israel

Shaare Zedek Medical Center /ID# 247319

Jerusalem, Jerusalem, Israel

ZIV Medical Center /ID# 226565

Safed, Northern District, Israel

Barzilai Medical Center /ID# 229156

Ashkelon, Southern District, Israel

Soroka University Medical Center /ID# 226570

Beersheba, Southern District, Israel

The Chaim Sheba Medical Center /ID# 226562

Ramat Gan, Tel Aviv, Israel

Tel Aviv Sourasky Medical Center /ID# 226564

Tel Aviv, Tel Aviv, Israel

Maccabi /ID# 246679

Haifa, Israel

...and 1 more locations

Outcomes

Primary Outcomes

Percentage of Participants Who Achieved Dermatology Life Quality Index (DLQI) 0 or 1

DLQI is a patient-administered, ten-question, quality of life questionnaire that covers six domains including symptoms and feelings, daily activities, leisure, work and school, personal relationships and treatment.

Time frame: Week 52

Secondary Outcomes

Percentage of Participants Who Achieved Dermatology Life Quality Index (DLQI) 0 or 1

Time frame: Up to approximately 104 weeks

Change From Baseline in Average Nightly Nocturnal Scratch Activity

Average nightly nocturnal scratch activity (number of scratch events, total scratch time, and scratch intensity) will be measured by a digital monitoring device.

Time frame: Baseline (Week 0) to Week 52

Percentage of Participants With Physician Assessment Static Psoriasis Global Assessment (sPGA) 0 or 1

Disease duration and disease severity will be assessed by sPGA.

Time frame: Up to approximately 104 weeks

Change From Baseline in Average Pruritus Numeric Rating Scale (PNRS)

PNRS is a patient reported score that assesses itch severity on a scale of 0 to 10, with 0 being "no itch" and 10 being "worst imaginable itch".

Time frame: Up to approximately 4 weeks

Change From Baseline in Medical Outcome Study Sleep Scale (MOS-SS)

Medical Outcomes Study Sleep Scale (MOS-Sleep) includes 12 items assessing sleep disturbance, sleep adequacy, somnolence, quantity of sleep, snoring, and awakening short of breath or with a headache over the past 4 weeks.

Time frame: Up to approximately 4 weeks

Change From Baseline in Psoriasis Symptoms Scale (PSS)

PSS is a 4-item scale designed to measure patient-reported psoriasis symptoms. The PSS consists of four items assessing severity of pain, itching, redness, and burning during the past 24 h. A 5-point severity scale was used as follows: 0 = none, 1 = mild, 2 = moderate, 3 = severe, 4 = very severe.

Time frame: Up to approximately 104 weeks

Change From Baseline in Dermatology Life Quality Index (DLQI)

Time frame: Up to approximately 104 weeks

Change From Baseline in Work Productivity and Activity Impairment (WPAI)

WPAI measures the effect of general health and symptom severity on work productivity and regular activities during the past 7 days.

Time frame: Up to approximately 104 weeks

Percentage of Participants With Change From Baseline DLQI > Minimal Clinically Important Difference (MCID)

Time frame: Up to approximately 104 weeks

Percentage of Participants With Durability of Response Among sPGA Responders ar Week 24

Durability of response is measured by the maintenance of the sPGA 0/1 at weeks 52 and 104.

Time frame: Up to approximately 104 weeks

Number of Participants With Adverse Events (AEs)

An adverse event (AE) is defined as any untoward medical occurrence in a patient which does not necessarily have a causal relationship with this treatment. The investigator assesses the relationship of each event to the use of study. A serious adverse event (SAE) is an event that results in death, is life-threatening, requires or prolongs hospitalization, results in a congenital anomaly, persistent or significant disability/incapacity or is an important medical event that, based on medical judgment, may jeopardize the participant and may require medical or surgical intervention to prevent any of the outcomes listed above.

Time frame: Up to approximately 104 weeks