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NCT07330934TerminatedPhase 2

A Study to Evaluate Efficacy and Safety of IBI356 in Participants With Moderate to Severe Atopic Dermatitis

A Multi-Center, Randomized, Double-Blind, Parallel, Placebo-Controlled Phase 2 Study to Evaluate the Efficacy and Safety of IBI356 in Adult Participants With Moderate to Severe Atopic Dermatitis

Source: ClinicalTrials.gov · Last updated 27 Oct 2026

Reason given: Sponsor Decision

Brief summary (registry, in English)

This is a multi-center, randomized, double-blind, parallel, placebo-controlled phase 2 clinical study. A total of 403 adult participants with moderate to severe AD are planned to be enrolled to evaluate efficacy, safety, PK characteristics, immunogenicity, and changes in PD characteristics of IBI356.

Status (registry)
Terminated
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
18 (actual)
First submitted
15 Dec 2025
Start date
31 Dec 2025
Primary completion date
18 Aug 2026
Lead sponsor
Innovent Biologics (Suzhou) Co. Ltd.
NCT number
NCT07330934

Who cannot take part

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

Prior treatment

  • Have received an organ or hematopoietic stem cell transplant.
  • Having received any of the specified therapy within the specified timeframe(s) prior to the baseline visit.
    • The above information is not intended to contain all considerations relevant to a potential participation in a clinical trial.

Other illness

  • Presence of diseases that may affect the safety or efficacy, including but not limited to psychistric disorders, central nervous system, cardiovascular system, digestive system, respiratory system, urinary system, and hematological or metabolic system diseases.
  • Known history of active tuberculosis or clinically suspected tuberculosis; or chest imaging suggesting evidence of suspected tuberculosis; or any other clinical evidence of latent tuberculosis.
  • Has known or suspected helminth or other parasitic infection.
  • History of malignancy, except excised or curatively treated localized basal cell carcinoma (BCC) or cutaneous squamous cell carcinoma (cSCC).
  • History of severe drug allergy or anaphylaxis.
  • Positive HBsAg; or positive HBcAb with positive HBV-DNA; or positive hepatitis C antibody with positive HCV-RNA; or positive treponema pallidum antibody; or positive HIV serology at screening.

Other

  • Fainting, hemophobia, or inability to tolerate venipuncture.
  • Women who are pregnant or breastfeeding, or female participants who have a positive pregnancy test at screening or randomization.

Who the study is looking for

  • Able to understand and sign the informed consent form (ICF);
  • Aged ≥ 18 years, male or female;
  • Diagnosis of AD for at least 1 year (defined by the American Academy of Dermatology Consensus Criteria);
  • EASI score of 16 or higher at baseline, vIGA-AD of 3 or 4 at baseline, AD involvement of 10% or more of BSA at baseline, weekly average of daily PP-NRS of ≥ 4 at baseline;
  • Participants with documented inadequate response to topical medications or for whom topical treatments are otherwise medically inadvisable.

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

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Peking University People's HospitalBeijingChinaUnknown status

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