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NCT Number: NCT07295509

A Study of Picankibart in Patients With Active Psoriatic Arthritis

This is a multicenter, randomized, double-blind, placebo-controlled Phase II/III clinical trial evaluating the efficacy and safety of picankibart (IBI112) in patients with active psoriatic arthritis (PsA). The study consists of two stages: Phase II dose-finding (n=90) and Phase III confirmatory (n=132). Participants will receive subcutaneous (SC) injections of either picankibart (200mg) or placebo with different dosing schedules, with placebo crossover to active treatment at Week 26. The Phase II portion will identify optimal dosing for Phase III, which will confirm efficacy. The study will evaluate improvements in joint symptoms, physical function, quality of life, and skin manifestations. Primary endpoint is percentage of participants who achieved an American College of Rheumatology (ACR) 20 Response at Week 24.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

The Second Affiliated Hospital of Zhejiang University School of Medicine

Hangzhou, Zhejiang, 310000, China

Location status: Recruiting

Location contact

Xiaoyong Man

CONTACT

[email protected]

+86 57187783753

Xiaoyong Man, M.D.

PRINCIPAL_INVESTIGATOR

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18-75 years
  • Diagnosed with PsA for ≥3 months, and meeting Classification Criteria for Psoriatic Arthritis (CASPAR) at screening
  • Having active PsA: ≥3 tender joints and ≥3 swollen joints at screening and baseline
  • Having active plaque psoriasis (≥1 lesion ≥2cm) or nail psoriasis, or a documented history of plaque psoriasis
  • Inadequate response or intolerance to prior NSAIDs or non-biologic DMARDs
  • Stable doses of protocol permitted background therapy (if any)

Exclusion criteria

  • Other inflammatory conditions that may affect the evaluation of the study drug
  • Prior treatment with >2 biologic agents
  • Recent use of prohibited medications (specific washout periods apply)
  • Non-plaque psoriasis forms or drug-induced psoriasis
  • Severe, progressive, or uncontrolled renal, hepatic, cardiovascular, pulmonary, gastrointestinal, endocrine, neurological, hematological, rheumatic (excluding PsA), psychiatric, or genitourinary conditions
  • Significant laboratory abnormalities
  • Pregnancy or breastfeeding

Treatment and study plan

Placebo

Other

Placebo administered SC at each scheduled dosing timepoint.

Picankibart

Drug

Picankibart administered SC at each scheduled dosing timepoint.

Primary outcomes

  1. Percentage of participants who achieved an American College of Rheumatology (ACR) 20 response

    Time frame: Week 26

    The ACR20 response is defined as ≥20% improvement in swollen joint count (66 joints) and tender joint count (68 joints) and ≥20% improvement in 3 of following 5 assessments: participant's assessment of pain using Visual Analog Scale (VAS; 0-100 millimeter [mm], 0 mm=no pain and 100 mm=worst possible pain), participant's global assessment of disease activity by using VAS (scale ranges from 0 mm to 100 mm, [0 mm= very well to 100 mm= very poor]), physician's global assessment of disease activity using VAS (scale ranges from 0 to 100), [0 = no arthritis to 100 = extremely active arthritis], participant's assessment of physical function measured by Health Assessment Questionnaire-Disability Index (HAQ-DI, defined as a 20-question instrument assessing 8 functional areas. The derived HAQ-DI ranges from 0, indicating no difficulty, to 3, indicating inability to perform a task in that area) and C-reactive protein (CRP).

Secondary outcomes

  1. Change from baseline in Disease Activity Score in 28 Joints (DAS28)-CRP score

    Time frame: Week 26, and from baseline to Week 56

    The DAS28-CRP is a measure of disease activity based on swollen and tender joint counts in 28 joints, CRP and the participant's global assessment of disease activity. The range of DAS28-CRP score is 0-10. Higher score means more disease activity.

  2. Percentage of participants who achieved an ACR50 response

    Time frame: Week 26, and from baseline to Week 56

    The ACR50 response is defined as ≥50% improvement in swollen joint count (66 joints) and tender joint count (68 joints) and ≥50% improvement in 3 of following 5 assessments: participant's assessment of pain using Visual Analog Scale (VAS; 0-100 millimeter [mm], 0 mm=no pain and 100 mm=worst possible pain), participant's global assessment of disease activity by using VAS (scale ranges from 0 mm to 100 mm, [0 mm= very well to 100 mm= very poor]), physician's global assessment of disease activity using VAS (scale ranges from 0 to 100), [0 = no arthritis to 100 = extremely active arthritis], participant's assessment of physical function measured by Health Assessment Questionnaire-Disability Index (HAQ-DI, defined as a 20-question instrument assessing 8 functional areas. The derived HAQ-DI ranges from 0, indicating no difficulty, to 3, indicating inability to perform a task in that area) and C-reactive protein (CRP).

  3. Percentage of participants who achieved an ACR70 response

    Time frame: Week 26, and from baseline to Week 56

    The ACR70 response is defined as ≥70% improvement in swollen joint count (66 joints) and tender joint count (68 joints) and ≥70% improvement in 3 of following 5 assessments: participant's assessment of pain using Visual Analog Scale (VAS; 0-100 millimeter [mm], 0 mm=no pain and 100 mm=worst possible pain), participant's global assessment of disease activity by using VAS (scale ranges from 0 mm to 100 mm, [0 mm= very well to 100 mm= very poor]), physician's global assessment of disease activity using VAS (scale ranges from 0 to 100), [0 = no arthritis to 100 = extremely active arthritis], participant's assessment of physical function measured by Health Assessment Questionnaire-Disability Index (HAQ-DI, defined as a 20-question instrument assessing 8 functional areas. The derived HAQ-DI ranges from 0, indicating no difficulty, to 3, indicating inability to perform a task in that area) and C-reactive protein (CRP).

  4. Change from baseline in Health Assessment Questionnaire-Disability Index (HAQ-DI)

    Time frame: Week 26, and from baseline to Week 56

    HAQ-DI measures improvement in physical function/disability. It is defined as a 20-question instrument assessing 8 functional areas. The derived HAQ-DI ranges from 0, indicating no difficulty, to 3, indicating inability to perform a task in that area.

  5. Change from baseline in Short Form Health Survey 36 (SF-36) Physical Component Summary (PCS) score

    Time frame: Week 26, and from baseline to Week 56

    The SF-36 Health determined participants' overall quality of life by assessing 1) limitations in physical functioning due to health problems; 2) limitations in usual role because of physical health problems; 3) bodily pain; 4) general health perceptions; 5) vitality; 6) limitations in social functioning because of physical or emotional problems; 7) limitations in usual role due to emotional problems; and 8) general mental health. Items 1-4 comprise the physical component of the SF-36. Scores on each item were summed and averaged (range = 0-100) and a positive change from Baseline indicates improvement.

  6. Enthesitis/dactylitis resolution rates

    Time frame: Week 26, and from baseline to Week 56

    Percentage of participants with complete resolution of enthesitis (inflammation at tendon/ligament attachments) or dactylitis (sausage-digit swelling).

  7. Percentage of participants who achieved 75%Psoriasis Area and Severity Index 75 response

    Time frame: From baseline to Week 56

    Percentage of participants who achieve at least 75% or 90% or 100% reduction in Psoriasis Area and Severity Index (PASI) score, assessing skin lesion severity in psoriatic arthritis patients.

  8. Change from baseline in van der Heijde-modified Total Sharp Score (vdH-mTSS)

    Time frame: Week 26 and Week 56

    The vdH-mTSS is a measure of change in joint health. X-rays of hands and feet are obtained at screening, Week 26 and Week 56. Totals for hands and feet for erosion scores (range 0 to 320) and joint space narrowing scores (range 0 to 208) were calculated and added to obtain the vdH-mTSS (range = 0 [normal] to 528 [maximal disease]). An increase in vdH-mTSS from baseline represents disease progression and/or joint worsening.

  9. Percentage of participants who experienced adverse events (AEs)

    Time frame: From baseline to Week 56

    An AE is any untoward medical occurrence, which does not necessarily have a causal relationship with treatment.

  10. Percentage of participants who experienced serious adverse events (SAEs)

    Time frame: From baseline to Week 56

    An SAE is an AE that results in death, is life-threatening, results in or prolongs hospitalization, results in congenital anomaly, persistent or significant disability/incapacity, spontaneous or elective abortion, or requires intervention to prevent a serious outcome.

  11. Maximum plasma concentration (Cmax) of picankibart

    Time frame: From baseline to Week 56

    Plasma concentration of picankibart is evaluated at each scheduled dosing timepoint. Cmax is the highest concentration of a drug in the blood.

  12. Area under the concentration-time curve (AUC) of picankibart

    Time frame: From baseline to Week 56

    Plasma concentration of picankibart is evaluated at each scheduled dosing timepoint. AUC represents the area under the concentration-time curve and gives insight into the extent of exposure to a drug and its clearance rate from the body.

  13. Percentage of participants who developed anti-drug antibody (ADA)

    Time frame: From baseline to Week 56

    ADAs are immune system-produced antibodies that specifically bind to therapeutic drugs, potentially altering their pharmacokinetics, efficacy, or safety.

  14. Percentage of participants who developed neutralizing antibody (NAb)

    Time frame: From baseline to Week 56

    NAbs are ADAs that inhibit the drug's biological function by blocking target interaction.

Study contacts

Contact information is provided by the study sponsor or research team.

Bingjing Feng

CONTACT

[email protected]

+86 18361923769

Sponsors and collaborators

Lead sponsor

Innovent Biopharmaceutical Technology (Hangzhou) Co., LTD.

Industry

Registry information

Official study title

A Multicenter, Randomized, Double-blind, Placebo-controlled Phase II/III Clinical Study to Evaluate the Efficacy and Safety of Picankibart in Patients With Active Psoriatic Arthritis

Important dates

Study start
2025
Primary completion
2029
Study completion
2029
First posted
Dec 19, 2025
Registry last updated
Mar 20, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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