A Study to Evaluate IBI112 in the Treatment of Psoriasis With Moderate to Severe Plaque Psoriasis

Last updated: October 28, 2024
Sponsor: Innovent Biologics (Suzhou) Co. Ltd.
Overall Status: Completed

Phase

3

Condition

Scalp Disorders

Rash

Warts

Treatment

placebo /IBI112

IBI112

Clinical Study ID

NCT05645627
CIBI112A301
  • Ages 18-75
  • All Genders

Study Summary

The purpose of this study is to evaluate the efficacy and safety of IBI112 in the treatment of participants with moderate to severe plaque-type psoriasis.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Diagnosis of plaque-type psoriasis with or without psoriatic arthritis for at least 6 months prior to first administration of any study agent

  2. Must be a candidate for phototherapy or systemic treatment for psoriasis (either newto treatment or having had previous treatment)

Exclusion

Exclusion Criteria:

  1. History of or current signs or symptoms of severe, progressive, or uncontrolledrenal, hepatic, hematological, gastrointestinal, endocrine, pulmonary, cardiac,neurologic, cerebral, or psychiatric disease

  2. Participant has history of erythrodermic psoriasis, generalized or localizedpustular psoriasis, medication-induced or medication-exacerbated psoriasis, or newonset guttate psoriasis

  3. Has received any therapeutic agent directly targeted to IL-17within 6 months of thefirst administration of study agent

  4. Has received any therapeutic agent directly targeted toTNF-a within 3 months of thefirst administration of study agent

  5. Has received any conventional therapeutic agent within 1 months of the firstadministration of study agent

  6. Has received any topic therapeutic agent within 2 weeks of the first administrationof study agent

Study Design

Total Participants: 500
Treatment Group(s): 2
Primary Treatment: placebo /IBI112
Phase: 3
Study Start date:
February 10, 2023
Estimated Completion Date:
August 01, 2024

Connect with a study center

  • Shanghai Skin Disease Hospital

    Shanghai, Shanghai 200443
    China

    Site Not Available

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