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Active, not recruiting Phase 2

ORKA-001 Versus Placebo in Patients With Moderate-to-Severe Plaque Psoriasis

NCT07090330 · tracked via the Priya Life Science USA tracker
Phase
Phase 2
Started
2025-07-18
Last updated
2026-07-01

Condition(s) studied

Plaque Psoriasis

Investigational drug(s) / intervention(s)

ORKA-001 Induction DosePlaceboORKA-001 Maintenance Dose →

ORKA-001 Induction Dose: ORKA-001 Induction Dose, administered by subcutaneous (SC) injection

Placebo: Placebo administered by subcutaneous (SC) injection

ORKA-001 Maintenance Dose: ORKA-001 Maintenance Dose, administered by subcutaneous (SC) injection

Study summary

This is a multicenter, randomized, double-blinded, placebo-controlled, proof-of-concept study to evaluate the efficacy, safety, tolerability, and pharmacokinetics of ORKA-001 in adult participants with moderate-to-severe plaque psoriasis.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Participants ≥ 18 years of age 2. Have a diagnosis of plaque psoriasis for \> 6 months 3. Have moderate-to-severe chronic plaque psoriasis defined as: 1. BSA ≥ 10%, and 2. PASI ≥ 12, and 3. IGA score of ≥ 3 on a 5-point scale 4. Candidate for systemic therapy or phototherapy 5. Women of childbearing potential must have a negative pregnancy test Exclusion Criteria: 1. Nonplaque forms of psoriasis (including guttate, erythrodermic, or pustular) or drug-induced psoriasis 2. Significant history or clinical manifestation of any metabolic, other dermatological, hepatic, renal, hematologic, pulmonary, cardiovascular, gastrointestinal, neurologic, respiratory, endocrine, or psychiatric disorder, or any infectious disease 3. History of malignancy, except for non-melanoma skin cancer or cancer curatively treated ≥ 5 years, without evidence of recurrence 4. A known hypersensitivity to any components of the ORKA-001 drug product 5. Women who are breastfeeding or plan to breastfeed during the study

Primary outcome measure(s)

  • Proportion of Participants Achieving 100% Reduction in PASI Score at Week 16 — Week 16
    The Psoriasis Area and Severity Index Score (PASI) is an evaluation tool that combines the assessment of the severity and the area affected by psoriasis into a single score ranging from 0 (no disease) to 72 (maximum disease).

Trial sites (26)

FacilityCityRegionStatus
Oruka Therapeutics Investigative Site Fountain Valley California
Oruka Therapeutics Investigative Site Los Angeles California
Oruka Therapeutics Investigative Site San Diego California
Oruka Therapeutics Investigative Site Santa Ana California
Oruka Therapeutics Investigative Site Santa Monica California
Oruka Therapeutics Investigative Site Cromwell Connecticut
Oruka Therapeutics Investigative Site Miami Florida
Oruka Therapeutics Investigative Site Rolling Meadows Illinois
Oruka Therapeutics Investigative Site Bowling Green Kentucky
Oruka Therapeutics Investigative Site Rockville Maryland
Oruka Therapeutics Investigative Site Boston Massachusetts
Oruka Therapeutics Investigative Site Detroit Michigan
Oruka Therapeutics Investigative Site New York New York
Oruka Therapeutics Investigative Site New York New York
Oruka Therapeutics Investigative Site Portland Oregon
Oruka Therapeutics Investigative Site Norfolk Virginia
Oruka Therapeutics Investigative Site Milwaukee Wisconsin
Oruka Therapeutics Investigative Site Edmonton Alberta
Oruka Therapeutics Investigative Site Edmonton Alberta
Oruka Therapeutics Investigative Site Surrey British Columbia
Oruka Therapeutics Investigative Site Hamilton Ontario
Oruka Therapeutics Investigative Site London Ontario
Oruka Therapeutics Investigative Site Markham Ontario
Oruka Therapeutics Investigative Site Peterborough Ontario
Oruka Therapeutics Investigative Site Toronto Ontario
Oruka Therapeutics Investigative Site Waterloo Ontario
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07090330 on ClinicalTrials.gov ↗ ← All trials in the USA