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Taking people in ChinaPhase 3

Tests D-2570 in adults with moderate to severe plaque psoriasis

Tests the drug D-2570 against a placebo in adults with moderate to severe plaque psoriasis.

Plain-language title generated from the registry record
Registry title: Evaluate the Efficacy and Safety of D-2570 in Subjects With Moderate to Severe Plaque Psoriasis

Key facts

Where
Beijing, ChinaSee the site
Phase
Phase 3

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 70 years old?

Source: NCT07130604, who can take part

Where in China

  • Peking University People's HospitalBeijing, ChinaTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
InventisBio Co., Ltd
Trial code
NCT07130604
Record updated
9 December 2025
Original description
This study is a randomized, double-blind, placebo-controlled multicenter clinical trial targeting subjects with moderate to severe plaque psoriasis.Read full original descriptionShow less

A Multicenter, Randomized, Double-Blind, Placebo-Controlled Phase III Study to Evaluate the Efficacy and Safety of D-2570 in Subjects With Moderate to Severe Plaque Psoriasis

This study is a randomized, double-blind, placebo-controlled multicenter clinical trial targeting subjects with moderate to severe plaque psoriasis.

Inclusion: Subject voluntarily takes part in the study after being fully informed,signs a written ICF, and agrees to follow procedures specified in the study protocol; Plaque psoriasis assessed by the investigator as suitable for systemic treatment and stable (defined as stable as no significant outbreak of morphological change or disease activity assessed by the investigator) for at least 6 months prior to signing informed consent; During the screening period and before taking the investigational drug for the first time, psoriatic surface area (BSA) ≥10%, PGA score ≥ 3, PASI score ≥ 12; Hematology, Blood chemistry and Urinalysis examination were basically normal.

Exclusion: Erythrodermic psoriasis, pustular psoriasis, guttate psoriasis, reverse psoriasis, drug-induced psoriasis; History of herpes zoster/herpes simplex, or presence of herpes zoster/herpes simplex infection during the screening period; Have a history of tuberculosis, or active tuberculosis, or latent tuberculosis, or suspected clinical manifestations of tuberculosis infection; Other conditions that the investigator considers inappropriate for participation in the study; Have other skin lesions that affect the evaluation of treatment outcomes, such as eczema.

ClinicalTrials.gov NCT07130604