Phase 2 Psoriasis Trial, Recruiting NCT07314060 Sponsor: Chia Tai Tianqing Pharmaceutical Group Co., Ltd. Condition: Psoriasis
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Phase 2 Psoriasis Trial, Recruiting

NCT07314060
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People aged 18 to 75 years old at the time of screening, of any gender
  • People who have been diagnosed with Generalized Pustular Psoriasis (GPP) based on specific criteria set by a 2017 international medical expert group (ERASPEN)
  • People who are currently experiencing an acute (sudden/active) flare-up of GPP
  • People who are able to read, understand, and are willing to sign a consent form agreeing to take part
  • People who are willing to attend all required study visits and follow study procedures
  • Women who are able to become pregnant must agree to use contraception throughout the study and for 6 months after the study ends

Who may not be able to join:

  • People whose pustules (pus-filled skin spots) appear only on raised psoriasis plaques, rather than as the generalised (widespread) GPP pattern
  • People who have another skin condition or other medical condition that might make it difficult for the study doctor to assess how well the treatment is working
  • People who have a severe, worsening, or uncontrolled medical condition that the study doctor considers unsuitable for participation
  • People who have abnormal blood test results for certain viruses during the screening period
  • People whose chest X-ray shows active tuberculosis (TB), who have had close contact with someone with active TB in the past 6 months, or who test positive on a specific TB blood test (IGRA)
  • People who were hospitalised due to a serious infection in the 2 months before the study start
  • People who, in the study doctor's assessment, needed antibiotics, antifungal, or antiviral medicines taken throughout the body (not just on the skin) within 2 weeks before the study start
  • People who have had a rare or unusual ("opportunistic") infection in the 6 months before the study start
  • People who received a live or weakened live vaccine within 12 weeks before the study start
  • People who had a major surgical procedure within 4 weeks before the study start, or who have a major surgery planned during the study period
  • People who received a blood transfusion within 4 weeks before the study start
  • People who took part in another clinical trial of a drug or medical device within 4 weeks before the study start
  • People who have a known or suspected condition — present from birth or developed later — that weakens the immune system
  • People who have any currently active cancer, or who have a history of cancer of any type
  • People with alcohol dependence, drug dependence, or known dependence on any specific medicine
  • Women who are pregnant or currently breastfeeding
  • People who are unable to tolerate receiving medicine through an intravenous (IV) drip into a vein

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 7 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Phone: 13693058190

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Chia Tai Tianqing Pharmaceutical Group Co., Ltd.
Registry
ClinicalTrials.gov
Start date
19 March 2026
Est. completion
1 December 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Percentage of patients with a score of 0 for the pustule subterm

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 7 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov