drugset / Trial / NCT07290569

Dose Ranging Study of ORKA-001 in Patients With Moderate-to-Severe Plaque Psoriasis

NCT07290569 ↗

Phase 2 Recruiting 160 enrolled Oruka Therapeutics, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

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

Timeline

Start
2025-12-03
Primary completion
2027-06
Completion
2028-12

Drugs

EvaluationDrugModalityDoseRoute
Subject ORKA-001 Unknown 37.5 mg Subcutaneous
Subject ORKA-001 Unknown 300 mg Subcutaneous
Subject ORKA-001 Unknown 600 mg Subcutaneous

Indications