A Study in Patients with Moderate to Severe Plaque Psoriasis to Evaluate the Efficacy and Safety of ESK-001
a study on Psoriasis
Summary
- Eligibility
- for people ages 18 years and up (full criteria)
- Location
- at San Diego, California and other locations
- Dates
- study startedcompletion around
Description
Summary
The goal of this clinical trial is to learn if ESK-001 works to treat moderate to severe plaque psoriasis. The main questions it aims to answer are:
- Does ESK-001 reduce the severity of people's psoriasis?
- How safe is ESK-001 in people with moderate to severe plaque psoriasis?
The study includes 2 comparators: a placebo control (a 'dummy' tablet that does not contain the medicine ESK-001 but looks just like it) and an active control (apremilast, which is a medicine approved to treat psoriasis).
People taking part in this study must be men or women aged at least 18 years and have had plaque psoriasis for at least 6 months, currently moderate to severe.
Participants will:
- take drug every day for 24 weeks.
- visit the clinic for checkups and tests.
- fill out questionnaires about their psoriasis, itch severity, and change in quality of life.
- be assessed for health issues and side effects, physical examinations, vital signs, heart electrical activity measurements, and psychological health.
- provide blood and urine samples.
Official Title
A Multicenter, Randomized, Double-Blind, Placebo and Active Comparator Controlled Phase 3 Study in Patients with Moderate to Severe Plaque Psoriasis to Evaluate the Efficacy and Safety of ESK-001 (ONWARD2)
Keywords
Plaque Psoriasis, Psoriasis, Apremilast, ESK-001
Eligibility
You can join if…
Open to people ages 18 years and up
- Males or females, age ≥18 years
- Diagnosis of plaque psoriasis for ≥6 months
- Plaques covering ≥10% of BSA
- PASI ≥12
- sPGA ≥3
- Women of childbearing potential (WOCBP) and males who are sexually active with WOCBP must agree to adhere to highly effective methods of contraception
You CAN'T join if...
- Nonplaque psoriasis or other inflammatory skin conditions
- Immune-mediated conditions commonly associated with psoriasis (eg inflammatory bowel disease). Patients with psoriatic arthritis may participate
- Pregnant, lactating, or planning to get pregnant during the study
- Use of drugs prior to Study Day 1 that treat or may affect psoriasis:
- Topical within 2 weeks
- Phototherapy or any systemic treatments within 4 weeks
- Any biologic agent targeted to IL-12 or IL-23 within 6 months, oral IL-12 or IL-23 or TNFα inhibitor within 2 months, or IL-17 within 4 months
- Systemic immunosuppressants or immunomodulatory drugs within 4 weeks
- Modulators of B cells within 6 months, or T cells within 3 months
- JAK inhibitors or TYK2 inhibitors within 4 weeks
- PDE4 inhibitor within 2 months
- Any investigational agent, within 30 days or 5 half-lives or is currently enrolled in an investigational study
- Lack of clinical response to a TYK2, IL-12, or IL-23 targeted psoriasis treatment
- Patients with QTcF >450 msec (males) or >470 msec (females) at Screening
- Unstable cardiovascular disease, defined as a recent clinical deterioration or a cardiac hospitalization within the last 3 months
- Evidence of recent or recurrent herpes zoster or herpes simplex viral infection
- Evidence of active infection or positive test result for hepatitis B, hepatitis C, HIV or TB
- History of serious bacterial, fungal, or viral infections that led to hospitalization, or any recent serious infection requiring antibiotic treatment
- Any history of known or suspected congenital or acquired immunodeficiency state or condition that would compromise the patient's immune status
- Lab abnormalities indicating significant renal, hepatic or bone marrow dysfunction
- History of any immune-mediated or inflammatory medical condition for which patient requires current systemic corticosteroids
Locations
- UC San Diego
accepting new patients
San Diego California 92122 United States - Southern California Clinical Research
accepting new patients
Santa Ana California 92701 United States
Details
- Status
- accepting new patients
- Start Date
- Completion Date
- (estimated)
- Sponsor
- Alumis Inc
- ID
- NCT06588738
- Phase
- Phase 3 Psoriasis Research Study
- Study Type
- Interventional
- Participants
- Expecting 840 study participants
- Last Updated
Please contact me about this study
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Thank you!
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