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NCT07474792Active, not recruitingPhase 2

Dose Ranging Study of ORKA-002 in Patients With Moderate-to-Severe Plaque Psoriasis

A Multicenter, Randomized, Double-Blinded, Placebo- Controlled, Dose-Range Finding Study to Evaluate the Efficacy, Safety, Tolerability, and Pharmacokinetics of ORKA-002 in Participants With Moderate-to-Severe Plaque Psoriasis

Source: ClinicalTrials.gov · Last updated 16 Oct 2026

Brief summary (registry, in English)

This is a multicenter, randomized, double-blinded, placebo-controlled, dose-range finding study to evaluate the efficacy and safety of ORKA-002 in adult participants with moderate-to-severe plaque psoriasis.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
160 (estimated)
First submitted
11 Mar 2026
Start date
19 Mar 2026
Primary completion date
31 Oct 2027
Lead sponsor
Oruka Therapeutics, Inc.
Diseases
Psoriasis
NCT number
NCT07474792

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 160
  • From 19 Mar 2026 to the primary completion date, 31 Oct 2027
  • 37 sites in 2 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Nonplaque forms of psoriasis (including guttate, erythrodermic, or pustular) or drug-induced psoriasis)

Other illness

  • 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
  • A known hypersensitivity to any components of the ORKA-002 drug product

Age

  • History of malignancy, except for non-melanoma skin cancer or cancer curatively treated ≥ 5 years, without evidence of recurrence

Other

  • Women who are breastfeeding or plan to breastfeed during the study

Who the study is looking for

  • Participants ≥ 18 and \< 80 years of age at the time of consent
  • Have a diagnosis of plaque psoriasis for \> 6 months
  • Have moderate-to-severe chronic plaque psoriasis defined as:
    • BSA ≥ 10%, and
    • PASI ≥ 12, and
    • IGA score of ≥ 3 on a 5-point scale
  • Candidate for systemic therapy or phototherapy
  • Women of childbearing potential must have a negative pregnancy test

Age in the registry: 18 years to 79 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (37)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Oruka Therapeutics Investigative Site
Coordinator of this site? Confirm its status
BarrieCanadaUnknown status
Oruka Therapeutics Investigative Site
Coordinator of this site? Confirm its status
EdmontonCanadaUnknown status
Oruka Therapeutics Investigative Site
Coordinator of this site? Confirm its status
LondonCanadaUnknown status
Oruka Therapeutics Investigative Site
Coordinator of this site? Confirm its status
North BayCanadaUnknown status
Oruka Therapeutics Investigative Site
Coordinator of this site? Confirm its status
PeterboroughCanadaUnknown status
Oruka Therapeutics Investigative Site
Coordinator of this site? Confirm its status
SaskatoonCanadaUnknown status
Oruka Therapeutics Investigative Site
Coordinator of this site? Confirm its status
SurreyCanadaUnknown status
Oruka Therapeutics Investigative Site
Coordinator of this site? Confirm its status
TorontoCanadaUnknown status
Oruka Therapeutics Investigative Site
Coordinator of this site? Confirm its status
WaterlooCanadaUnknown status
Oruka Therapeutics Investigative Site
Coordinator of this site? Confirm its status
Ann ArborUnited StatesUnknown status
Oruka Therapeutics Investigative Site
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BexleyUnited StatesUnknown status
Oruka Therapeutics Investigative Site
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BirminghamUnited StatesUnknown status
Oruka Therapeutics Investigative Site
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BostonUnited StatesUnknown status
Oruka Therapeutics Investigative Site
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CharlestonUnited StatesUnknown status
Oruka Therapeutics Investigative Site
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CromwellUnited StatesUnknown status
Oruka Therapeutics Investigative Site
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DallasUnited StatesUnknown status
Oruka Therapeutics Investigative Site
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DetroitUnited StatesUnknown status
Oruka Therapeutics Investigative Site
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ElmhurstUnited StatesUnknown status
Oruka Therapeutics Investigative Site
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Fountain ValleyUnited StatesUnknown status
Oruka Therapeutics Investigative Site
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HoustonUnited StatesUnknown status
Oruka Therapeutics Investigative Site
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Los AngelesUnited StatesUnknown status
Oruka Therapeutics Investigative Site
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MiamiUnited StatesUnknown status
Oruka Therapeutics Investigative Site
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MilfordUnited StatesUnknown status
Oruka Therapeutics Investigative Site
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Mill CreekUnited StatesUnknown status
Oruka Therapeutics Investigative Site
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New BrightonUnited StatesUnknown status
Oruka Therapeutics Investigative Site
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New YorkUnited StatesUnknown status
Oruka Therapeutics Investigative Site
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OmahaUnited StatesUnknown status
Oruka Therapeutics Investigative Site
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PhoenixUnited StatesUnknown status
Oruka Therapeutics Investigative Site
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PortlandUnited StatesUnknown status
Oruka Therapeutics Investigative Site
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Rolling MeadowsUnited StatesUnknown status
Oruka Therapeutics Investigative Site
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San DiegoUnited StatesUnknown status
Oruka Therapeutics Investigative Site
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Santa AnaUnited StatesUnknown status
Oruka Therapeutics Investigative Site
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Santa MonicaUnited StatesUnknown status
Oruka Therapeutics Investigative Site
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WarrenUnited StatesUnknown status
Oruka Therapeutics Investigative Site
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WarrentonUnited StatesUnknown status
Oruka Therapeutics Investigative Site
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WebsterUnited StatesUnknown status
Oruka Therapeutics Investigative Site
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WilmingtonUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.