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

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-79
SponsorOruka Therapeutics, Inc.

About this trial

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.

Eligibility criteria

Qualifiers

Participants ≥ 18 and < 80 years of age at the time of consent

Have a diagnosis of plaque psoriasis for > 6 months

BSA ≥ 10%, and

PASI ≥ 12, and

Disqualifiers

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

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

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

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

Trial design

Treatments tested in this trial

  • ORKA-002
  • Placebo

Treatment groups

160 Participants
are divided into 4 treatment groups

Sponsors and collaborators