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Completed

NCT Number: NCT06085521

A Study of LNK01001 Capsule in Patients With Moderate to Severe Atopic Dermatitis

Participants who meet eligibility criteria will be randomized in a 1:1:1 ratio to receive a twice daily oral LNK01001 dose A or LNK01001 dose B or matching placebo for 12 weeks.

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Key information

About this study

The study was to include a 12-week double-blind treatment period. Participants who met eligibility criteria were to be randomized in a 1:1:1 ratio to one of the three treatment groups.

Group 1:LNK01001 dose A (Day 1 to Week 12) Group 2:LNK01001 dose B (Day 1 to Week 12) Group 3: Matching placebo (Day 1 to Week 12)

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • participants between ≥ 18 and ≤75 years of age.
  • subjects meet Hanifin and Rajka criteria.
  • subjects meet moderate to severe AD criteria.
  • inadequate response to topical treatment or systemic treatment for AD within 6 months before screening.

Exclusion criteria

  • current use of topical treatment for AD within 2 weeks before baseline visit.
  • prior exposure to Janus Kinase (JAK) inhibitor.
  • prior exposure to phototherapy, tanning bed, or any other light emitting device treatment within 4 weeks before baseline visit.
  • Prior exposure to any Biologic treatment including Dupilumab, Omalizumab within 3 months before baseline visit.
  • Any significant clinical and laboratory abnormalities, as determined by the Investigator, may affect the safety of the subjects, including but not limited to:WBC<3×10e9/L, neutrophil<1.2×10e9/L, platelet<100×10e9/L, hemoglobin<85 g/L; Aspartate aminotransferase or alanine aminotransferase>1.5×ULN, or total bilirubin>1.5×ULN; Serum creatinine>1.2×ULN.

Treatment and study plan

LNK01001 Dose A

Drug

Capsules taken orally

LNK01001 Dose B

Drug

Capsules taken orally

Placebo

Drug

Capsules taken orally

Primary outcomes

  1. Percent Change from Baseline in Eczema Area and Severity Index (EASI) Score

    Time frame: week 12

    EASI is a tool used to measure the extent (area) and severity of atopic eczema based on assessments of the head/neck, trunk, upper limbs and lower limbs. For each region the area score is recorded as the percentage of skin affected by eczema. For each region, the severity score is calculated as the sum of the intensity scores (scored as none [0], mild [1], moderate [2], or severe [3]) for redness (erythema, inflammation), thickness (induration, papulation, swelling - acute eczema), scratching (excoriation), and lichenification (lined skin, prurigo nodules - chronic eczema).

    The total EASI score for each region is calculated by multiplying the severity score by the area score, with adjustment for the proportion of the body region to the whole body. The final EASI score is the sum of the 4 region scores and ranges from 0 to 72 where higher scores represent worse disease.

Secondary outcomes

  1. Percentage of Participants Who Achieved a 75% Reduction in EASI Score (EASI 75)

    Time frame: Week 4,8,12

    An EASI 75 response is defined as participants with at least a 75% reduction (improvement) in EASI score relative to the Baseline value

  2. Percentage of Participants Achieving an Investigator Global Assessment (IGA) response

    Time frame: Week 4,8,12

    IGA response defined as an IGA score of 0 (clear) or 1 (almost clear) with a reduction from baseline of ≥ 2 points

  3. Percent Change from Baseline in EASI Score

    Time frame: Week 4,8

    EASI is a tool used to measure the extent (area) and severity of atopic eczema based on assessments of the head/neck, trunk, upper limbs and lower limbs. For each region the area score is recorded as the percentage of skin affected by eczema. For each region, the severity score is calculated as the sum of the intensity scores (scored as none [0], mild [1], moderate [2], or severe [3]) for redness (erythema, inflammation), thickness (induration, papulation, swelling - acute eczema), scratching (excoriation), and lichenification (lined skin, prurigo nodules - chronic eczema).

    The total EASI score for each region is calculated by multiplying the severity score by the area score, with adjustment for the proportion of the body region to the whole body. The final EASI score is the sum of the 4 region scores and ranges from 0 to 72 where higher scores represent worse disease.

  4. Percentage of Participants Achieving a Reduction of ≥ 3 Points From Baseline in Worst Pruritus Numerical Rating Scale (NRS)

    Time frame: Week 4,8,12

    Participants were asked to rate itch (pruritus) intensity at its worst during the past 24 hours on a daily basis using an 11-point scale from 0 (no itch) to 10 (worst imaginable itch). Pruritus NRS was analyzed based on weekly rolling averages of daily scores.

  5. Change From Baseline in Worst Pruritus Numerical Rating Scale(NRS) Score

    Time frame: Week 4,8,12

    Participants were asked to rate itch (pruritus) intensity at its worst during the past 24 hours on a daily basis using an 11-point scale from 0 (no itch) to 10 (worst imaginable itch). Pruritus NRS was analyzed based on weekly rolling averages of daily scores.

  6. Percentage of Participants Achieving a Reduction of ≥ 2 Points From Baseline in Investigator Global Assessment (IGA)

    Time frame: Week 4,8,12

    IGA is a validated assessment instrument to rate the severity of atopic dermatitis globally, based on the following scale:

    0 - Clear: No inflammatory signs of AD;

    • - Almost clear: Barely perceptible erythema, induration/papulation and/or lichenification;
    • - Mild: Slight but definite erythema, induration/papulation and/or minimal lichenification. No oozing or crusting;
    • - Moderate: Clearly perceptible erythema, induration/papulation and/or lichenification, oozing or crusting may be present;
    • - Severe: Marked erythema, induration/papulation and/or lichenification; Oozing or crusting may be present.
  7. Percentage of Participants Who Achieved a 90% Reduction in EASI Score (EASI 90)

    Time frame: Week 4,8,12

    An EASI 90 response is defined as participants with at least a 90% reduction (improvement) in EASI score relative to the Baseline value

  8. Percentage of Participants Who Achieved a 50% Reduction in EASI Score (EASI 50)

    Time frame: Week 4,8,12

    An EASI 50 response is defined as participants with at least a 50% reduction (improvement) in EASI score relative to the Baseline value

  9. Percent Change from Baseline in Scoring Atopic Dermatitis (SCORAD) Score

    Time frame: Week 4,8,12

    SCORAD is a clinical tool used to assess the extent and severity of eczema (SCORing Atopic Dermatitis). The extent is assessed using the rule of 9 to calculate the affected area (A) as a percentage of the whole body (0-100%). The intensity part of the SCORAD (B) consists of 6 items: erythema, oedema/papulation, excoriations, lichenification, oozing/crusts and dryness, each graded on a scale from 0 (none) to 3 (severe), for a total score of 0 to 18. Subjective items (C) include daily pruritus and sleeplessness, each scored on a visual analogue scale (VAS) from 0 to 10 (total score 0-20). SCORAD is calculated as A/5 + 7B/2 + C, and ranges from 0 to 103 (worst). A negative change from Baseline indicates improvement.

  10. Change From Baseline in Dermatology Life Quality Index (DLQI) Score

    Time frame: Week 4,8,12

    The DLQI is a 10-item validated questionnaire used to assess the impact of AD disease symptoms and treatment on quality of life (QoL). It consists of 10 questions evaluating impact of skin diseases on different aspects of a participant's QoL over the prior week, including symptoms and feelings, daily activities, leisure, work or school, personal relationships, and the side effects of treatment. Each item is scored on a 4-point scale (0 = not at all/not relevant; 1 = a little; 2 = a lot; and 3 = very much).

    Item scores are added to provide a total score, ranging from 0 to 30, with higher scores indicating greater impairment of QoL.

  11. Change From Baseline in Patient Oriented Eczema Measure (POEM) Score

    Time frame: Week 4,8,12

    The POEM is a 7-item, validated questionnaire used to assess disease symptoms in both children and adults. Participants respond to 7 questions, including dryness, itching, flaking, cracking, sleep loss, bleeding, and weeping, each scored on a 5-point scale based on frequency of occurrence during the previous week: 0 = no days, 1 = 1 to 2 days, 2 = 3 to 4 days, 3 = 5 to 6 days, and 4 = all days. Item scores are added to provide a total score ranging from 0 (clear) to 28 (very severe atopic eczema). A change in POEM score of 3.4 points is considered the minimal clinically important difference.

Sponsors and collaborators

Lead sponsor

Lynk Pharmaceuticals Co., Ltd

Industry

Registry information

Official study title

A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficiency and Safety of LNK01001 Capsule in Patients With Moderate to Severe Atopic Dermatitis

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
Oct 17, 2023
Registry last updated
Oct 27, 2023

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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