Efficacy, Safety, Pharmacokinetics of ICP-488 in Patients With Moderate to Severe Plaque Psoriasis

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18-75
SponsorBeijing InnoCare Pharma Tech Co., Ltd.

About this trial

This is a multicenter, randomized, double-blind, placebo-controlled Phase III clinical study to evaluate the efficacy, safety, PK characteristics of ICP-488 in Chinese adults with moderate to severe plaque psoriasis.

Eligibility criteria

Qualifiers

Subjects voluntarily participate in this study and have signed informed consent.

Male or female subjects between the ages of 18 and 75 (including the threshold) at the time of signing the ICF.

History of plaque psoriasis ≥6 months at baseline.

Subjects need to receive systemic therapy and/or phototherapy.

Disqualifiers

The diagnosis was non-plaque psoriasis.

Subjects with concurrent skin diseases that the investigator believes would interfere with the study assessments.

Presence of infection or immune-related disease.

Subjects with a history of TB or at risk for TB.

Trial design

Treatments tested in this trial

  • ICP-488 Tablets
  • ICP-488 Placebo

Treatment groups

383 Participants
are divided into 2 treatment groups