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A Study to Evaluate the Efficacy, Safety, and Pharmacokinetic Profiles of TLL-018 in Patients With Moderate-to-Severe Atopic Dermatitis

A Phase II/III, Multicenter, Randomized, Double-Blind, Placebo-Controlled Clinical Study to Evaluate the Efficacy, Safety, and Pharmacokinetic Profiles of TLL-018 in Patients With Moderate-to-Severe Atopic Dermatitis

This is an operationally seamless Phase II/III, multicenter, randomized, double-blind, placebo-controlled trial in patients with moderate-to-severe atopic dermatitis (AD). The Phase II stage aims to preliminarily evaluate the efficacy of TLL-018 and identify the dose and sample size for the subsequent Phase III stage, which is designed to confirm the efficacy of TLL-018.

The primary outcome measures are the proportion of participants achieving EASI-75 (≥75% improvement in Eczema Area and Severity Index from baseline) at week 16, and the proportion of participants achieving an Investigator's Global Assessment (IGA) score of 0 or 1 with a ≥2-point reduction from baseline at week 16.

研究概览

研究类型

介入性

注册 (估计的)

390

阶段

  • 阶段2
  • 第三阶段

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Beijing、中国、100044
        • Peking University People's Hospital
        • 接触:
          • Jianzhong Zhang, MD
          • 电话号码:86-10- 88325472
          • 邮箱:rmzjz@126.com
        • 接触:
          • Cheng Zhou, MD

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  • The trial participant understands and voluntarily signs the informed consent form (ICF), and has the willingness and ability to complete the scheduled follow-up visits, treatment plans, laboratory tests, and other trial procedures required by the protocol.
  • Male or female trial participants aged ≥18 and ≤75 years at the time of signing the ICF.
  • Have a history of atopic dermatitis for at least 1 year at screening, and meet the Hanifin-Rajka diagnostic criteria.
  • At screening and randomization, meet the criteria for moderate-to-severe atopic dermatitis as assessed by the investigator, with all of the following 4 conditions met simultaneously: Eczema Area and Severity Index (EASI) ≥16; Investigator's Global Assessment (IGA) ≥3; Body Surface Area (BSA) affected by atopic dermatitis ≥10%; Weekly average of Worst Itch Numeric Rating Scale (WI-NRS) ≥4.

    5. In the investigator's judgment, have received topical treatment for atopic dermatitis within 6 months prior to screening with inadequate clinical response or intolerance, or require systemic therapy to control the disease.

    6. The trial participant is able and willing to regularly use a mild emollient without active ingredients twice daily for at least 7 consecutive days prior to randomization, and to continue using it throughout the study.

    7. Female trial participants of childbearing potential must not be pregnant or lactating, and may enter the study only after pregnancy test results are confirmed negative.

    8. Female trial participants of childbearing potential, male trial participants, and their partners must use adequate and effective contraceptive measures from the screening period until 90 days after the last dose, and must have no plans to donate sperm (males) or ova (females) from the screening period until at least 6 months after the last dose.

Exclusion Criteria:

  • Presence of any of the following diseases or medical histories:

    1. Inability to swallow investigational product, refractory nausea/vomiting, malabsorption, external biliary diversion; history of gastrointestinal perforation (excluding perforation secondary to appendicitis or mechanical trauma); gastrointestinal disorders impairing drug absorption or other malabsorption conditions.
    2. Concurrent active inflammatory skin diseases that may confound efficacy assessment.
    3. Current or prior lymphoproliferative disorders, or suggestive signs/symptoms including lymphadenopathy or splenomegaly.
    4. History of malignancy prior to screening, except for treated-and-cured non-melanoma skin cancer/basal-cell carcinoma, cervical carcinoma in-situ, or breast ductal carcinoma in-situ.
    5. Herpes zoster within 1 year before randomization; any prior disseminated or recurrent herpes zoster; any prior disseminated herpes simplex.
    6. Severe/systemic infections within 4 weeks pre-randomization requiring intravenous anti-infective therapy or resulting in infection-related hospitalization; or other active/recent infections judged by the investigator to confer unacceptable subject risk.
    7. Acquired or hereditary immunodeficiency disorders.
    8. Severe haematological diseases, or conditions predisposing to haemolysis or red-cell instability.
    9. Documented psychiatric disorders likely to impair trial compliance, or known poor adherence.
    10. Major surgery or severe trauma within 4 weeks pre-randomization, or planned major surgery during the trial.
    11. Prior or planned solid-organ transplantation (e.g., liver transplantation).
    12. History or evidence of high-risk cardiovascular/cerebrovascular disease.
  • Any screening laboratory abnormality meeting the following thresholds:

    1. Complete blood count: haemoglobin < 90 g/L; white-blood-cell count < 2.5 × 10⁹/L; absolute-neutrophil count < 1.5 × 10⁹/L; lymphocyte count < 0.8 × 10⁹/L; platelet count < 100 × 10⁹/L.
    2. Liver function: AST or ALT > 2 × upper-limit-of-normal (ULN); total bilirubin > 2 × ULN.
    3. Serum creatinine ≥ 1.2 × ULN.
    4. Coagulation: PT or APTT > ULN with clinical significance.
    5. Uncontrolled hypertension: SBP ≥ 160 mmHg and/or DBP ≥ 100 mmHg. Confirmatory measurement: if initial reading exceeds threshold, rest ≥ 5 minutes then re-measure once; use repeat value if below threshold.
    6. Uncontrolled dyslipidaemia: fasting total cholesterol ≥ 7.2 mmol/L, or fasting LDL-C ≥ 4.9 mmol/L, or fasting triglycerides > 5.6 mmol/L.
  • Tuberculosis-related exclusion criteria:

    1. History of active TB without documented clinical cure.
    2. Screening imaging (e.g., chest-CT) demonstrating active TB.
    3. Suspicious TB-related symptoms that cannot be ruled out by investigator (low-grade fever, cough, night-sweats, weight loss etc.).
    4. Latent tuberculosis infection (LTBI): positive TB assay (T-SPOT-TB, QuantiFERON-TB-Gold etc.) without active-TB signs/symptoms.
  • Progressive/uncontrolled renal, hepatic, haematological, gastrointestinal, endocrine, pulmonary, cardiovascular, neurological, psychiatric or cerebral disease; investigator judges participation poses unacceptable risk.
  • Known or suspected hypersensitivity to TLL-018 active substance, excipients, or agents of the same drug class.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:四人间

武器和干预

参与者组/臂
干预/治疗
实验性的:Arm A
TLL-018 10 mg. Dose selection for continuation into Stage 2 (Phase III) will be based on efficacy and safety data generated from Stage 1 (Phase II). This dose group may or may not be carried forward into Stage 2.
TLL-018 tablets taken orally 10 mg (1 tablet) twice daily
TLL-018 tablets taken orally 20 mg (2 tablets) twice daily
TLL-018 tablets taken orally 30 mg (3 tablets) twice daily
实验性的:Arm B
TLL-018 20 mg. Dose selection for continuation into Stage 2 (Phase III) will be based on efficacy and safety data generated from Stage 1 (Phase II). This dose group may or may not be carried forward into Stage 2.
TLL-018 tablets taken orally 10 mg (1 tablet) twice daily
TLL-018 tablets taken orally 20 mg (2 tablets) twice daily
TLL-018 tablets taken orally 30 mg (3 tablets) twice daily
实验性的:Arm C
TLL-018 30 mg. Dose selection for continuation into Stage 2 (Phase III) will be based on efficacy and safety data generated from Stage 1 (Phase II). This dose group may or may not be carried forward into Stage 2.
TLL-018 tablets taken orally 10 mg (1 tablet) twice daily
TLL-018 tablets taken orally 20 mg (2 tablets) twice daily
TLL-018 tablets taken orally 30 mg (3 tablets) twice daily
安慰剂比较:Arm D
Placebo. This arm will be used in both Stage 1 (Phase II) and Stage 2 (Phase III).
Placebo taken orally twice daily

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Proportion of trial participants achieving at least 75% improvement from baseline in Eczema Area and Severity Index (EASI-75) at Week 16
大体时间:Week 16
The Eczema Area and Severity Index (EASI) is a validated, physician-assessed tool used to measure the extent and severity of atopic dermatitis (eczema). The total score ranges from 0 to 72, with higher scores indicating more severe disease.
Week 16
Proportion of trial participants achieving an Investigator's Global Assessment (IGA) score of 0 or 1 with a reduction of ≥ 2 points at Week 16
大体时间:Week 16

The Investigator's Global Assessment (IGA) is a physician-reported, static measure used to rate the overall severity of atopic dermatitis at a given time point.

It typically uses a 5-point scale from 0 to 4: 0 = Clear, 4 = Severe.

Week 16

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年8月31日

初级完成 (估计的)

2029年9月30日

研究完成 (估计的)

2029年9月30日

研究注册日期

首次提交

2026年8月21日

首先提交符合 QC 标准的

2026年8月21日

首次发布 (实际的)

2026年8月25日

研究记录更新

最后更新发布 (实际的)

2026年8月25日

上次提交的符合 QC 标准的更新

2026年8月21日

最后验证

2026年8月1日

更多信息

与本研究相关的术语

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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