Phase 1 Study of QX-4533 in Healthy Volunteers and Patients With Moderate-to-Severe Atopic Dermatitis
2026年9月13日 更新者:QuantX Biosciences, Inc.
A Phase 1 Study With a Single Ascending Dose-escalation in Healthy Volunteers to Assess the Safety, Tolerability, and Pharmacokinetics of QX-4533 and a Randomized, Double-Blind, Placebo-Controlled, Parallel Group to Assess the Safety, Pharmacokinetics, and Preliminary Efficacy of QX-4533 in Participants With Moderate-to-Severe Atopic Dermatitis
The goal of this clinical trial is to evaluate the safety and tolerability of QX-453, an investigational treatment, in healthy Chinese volunteers and patients with moderate-to-severe atopic dermatitis.
The study will assess how the drug is absorbed and processed by the body, and check for any side effects.
Participants will receive single or repeated oral doses of QX-453 under close medical supervision, with regular safety and clinical assessments throughout the trial.
研究概览
研究类型
介入性
注册 (估计的)
84
阶段
- 阶段1
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。
学习联系方式
- 姓名:Yan Liu
- 电话号码:+86 18782948571
- 邮箱:yan.liu16@tigermedgrp.com
学习地点
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Shanghai Municipality
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Shanghai、Shanghai Municipality、中国、200040
- 招聘中
- Huashan Hospital, Fudan University
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首席研究员:
- Jing Zhang
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首席研究员:
- Wenyu Wu
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接触:
- Jing Zhang
- 电话号码:021-52887976
- 邮箱:Zhangj_fudan@163.com
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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
- 孩子
- 成人
- 年长者
接受健康志愿者
是的
描述
Inclusion Criteria:
- Part 1: Eligibility Criteria for HVs
Inclusion criteria:
Participants are eligible to be included in Part 1 of the study only if all of the following criteria apply:
- Fully understanding the purpose, nature, method, and possible adverse reactions of the trial, voluntarily participating as a clinical trial participant, and signing the ICF;
- Being willing and able to comply with the study protocol and cooperate in completing the visit procedures throughout the study;
- Males and females aged 18 to 55 years (inclusive, at the time of signing the ICF) at screening;
- Body mass index (BMI) of 18 to 28 kg/m2 (inclusive); weight not less than 50 kg for male and 45 kg for female;
- Participants in good general health as judged by the Investigator based on their medical history, physical examination, vital signs, 12-lead ECG, and clinical laboratory findings (normal or abnormal but not clinically significant) at screening and on Day -1;
- Female participants must be non-pregnant and non-lactating, and female participants of childbearing potential must agree to use contraception from the signing of the ICF until at least 40 days after the last dose (10 days [approximately 5 t1/2] plus 30 days). Male participants with female partners of childbearing potential must agree to use contraception from the signing of the ICF until at least 100 days after the last dose (10 days [approximately 5 t1/2] plus a 90-day spermatogenesis cycle) (by taking medically approved effective contraceptive measures. See Appendix 3 Contraceptive Measures and Definition of Women of Childbearing Potential for details). Male participants must refrain from donating sperm for at least 150 days after the last dose. Female participants must refrain from donating eggs for at least 40 days after the last dose.
Part 2: Eligibility Criteria for Participants with AD Inclusion Criteria
Participants are eligible to be included in Part 2 of the study only if all of the following criteria apply:
- Fully understanding the purpose, nature, method, and possible adverse reactions of the trial, voluntarily participating as a participant, and signing the ICF;
- Being willing and able to comply with scheduled visits, treatment plan, laboratory tests, and other study-related procedures and questionnaires, including completing the electronic diaries and questionnaires, for the duration of the study as required by the study protocol;
- Males and females aged 18 to 65 years (inclusive) at screening;
- Participants with chronic AD diagnosed by the Eichenfield revised criteria of Hannifin and Rajka and with a confirmed diagnosis for at least one year prior to the screening visit;
- Participants with inadequate response, intolerance, or contraindication to topical corticosteroids and/or topical calcineurin inhibitors;
- Participants must be able and willing to regularly use a mild, inactive ingredient-free emollient twice daily for at least 7 consecutive days before randomization and continue to use it during the study;
- Female participants must be non-pregnant and non-lactating, and female participants of childbearing potential must agree to use contraception from the signing of the ICF until at least 40 days after the last dose (10 days [approximately 5 t1/2] plus 30 days). Male participants with female partners of childbearing potential must agree to use contraception from the signing of the ICF until at least 100 days after the last dose (10 days [approximately 5 t1/2] plus a 90-day spermatogenesis cycle) (by taking medically approved effective contraceptive measures. See Appendix 3 Contraceptive Measures and Definition of Women of Childbearing Potential for details). Male participants must refrain from donating sperm for at least 150 days after the last dose. Female participants must refrain from donating eggs for at least 40 days after the last dose.
Exclusion Criteria:
Part 1:
- Participants who are mentally or legally incapacitated, have a history of psychosis, or have significant emotional or psychological problems at the time of the study according to the Investigator;
- Participants with dysphagia, oesophageal stenosis, or gastrointestinal diseases that cause clinically significant symptoms such as nausea, vomiting, diarrhoea, or malabsorption syndrome, or with a history of severe vomiting or diarrhoea within one week before the screening period;
- Participants who have previously undergone surgeries that the Investigator deems may affect drug absorption, distribution, metabolism, or excretion (e.g., gastrectomy, cholecystectomy, gastric bypass, duodenal resection, colectomy);
- Participants with a history of any ongoing medical condition requiring treatment with prescription medication within two weeks prior to screening;
- Participants with a history of any infection requiring treatment with a prescription anti-infective in the past 4 weeks prior to screening;
- Use of any prescription medications, health supplements, herbal supplements, traditional Chinese medicines (TCMs), Chinese patent medicines, or over-the-counter (OTC) medications (except for routine vitamin supplements) within two weeks prior to dosing;
- Participants with history of malignancy, except fully resolved basal cell carcinoma (BCC), squamous cell carcinoma (SCC), or in situ carcinoma of the uterine cervix;
- History of invasive, opportunistic infections such as histoplasmosis, listeriosis, coccidioidomycosis, candidiasis, Pneumocystis jirovecii pneumonia, and aspergillosis (including resolved cases); John Cunningham (JC) virus (progressive multifocal leukoencephalopathy), or any active or parasitic infection in the prior 30 days;
- Participants who have undergone surgery, experienced significant blood loss, or donated more than one unit of whole blood (200 mL) within 8 weeks prior to screening, or who have donated more than one unit of plasma (100 mL) within 7 days prior to screening, or who plan to donate blood during the trial;
- Participants who have smoked more than 10 cigarettes (or equivalent nicotine-containing products) per week on average within 90 days prior to screening and are unwilling to quit smoking during hospitalization or restrict smoking to no more than 10 cigarettes (or equivalent nicotine-containing products) per week during the post-discharge period;
- Participants who have consumed more than 14 units of alcohol per week (1 unit = 360 mL of beer; 150 mL of wine; 45 mL of spirits) within 90 days prior to screening;
- Participants who have consumed tea, coffee and/or other caffeine-containing beverages, grapefruit juice, or other beverages that affect liver enzyme activity (more than 8 cups, 1 cup = 250 mL) daily within 3 months prior to screening or are unable to abstain during the trial;
- Participants with special dietary requirements or unable to follow a uniform diet (such as intolerance to standard meal foods, etc.); or participants who refuse to stop consuming pomelo/grapefruit or drinks made thereof, coffee, tea, or any food or beverage containing caffeine or rich in xanthine (such as animal offal, seafood, soy products, etc.) from 48 hours prior to dosing until the EOS;
- Participants who drink alcohol or perform strenuous physical activities (including but not limited to strenuous weightlifting, running, and cycling) from 48 hours prior to dosing until the EOS;
- Participants who are unable to complete the study due to their own reasons or are judged by the Investigator to be unsuitable for study participation for other reasons;
Part 2:
- Participants who have required oral or intravenous antibiotics, anti-virals, anti-parasitics, anti-protozoals, or anti-fungals for the treatment of chronic or acute infection within 4 weeks prior to the screening visit;
- Planned major surgical procedure during the length of the study;
- Participants who are unable to complete the study due to their own reasons or are judged by the Investigator to be unsuitable for study participation for other reasons;
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 |
|---|---|
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实验性的:QX4533
oral tablets administered once daily
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QX-4533, an oral investigational drug, administered as oral tablets in single or repeated dose escalation schedules for moderate-to-severe atopic dermatitis patients and healthy volunteers
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安慰剂比较:QX4533 Placebo
oral tablets administered once daily
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QX-4533 placebo, an oral investigational drug, administered as oral tablets in single or repeated dose escalation schedules for moderate-to-severe atopic dermatitis patients and healthy volunteers
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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 |
|---|---|---|
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Incidence of Treatment-emergent Adverse Events (TEAEs)
大体时间:From enrollment through the safety follow-up visit (up to Day 9 [Part 1] and Day 43 [Part 2])
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Number of Participants with Treatment-emergent Adverse Events (TEAEs)
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From enrollment through the safety follow-up visit (up to Day 9 [Part 1] and Day 43 [Part 2])
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Number of Participants with Clinically Significant Laboratory Parameter Changes
大体时间:From enrollment through the safety follow-up visit (up to Day 9 [Part 1] and Day 43 [Part 2])
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Number of Participants with Clinically Significant Change from Baseline in Clinical Laboratory Parameters
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From enrollment through the safety follow-up visit (up to Day 9 [Part 1] and Day 43 [Part 2])
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次要结果测量
结果测量 |
大体时间 |
|---|---|
|
Maximum Observed Plasma Concentration (Cmax)
大体时间:Day 1 (Part 1); Day 1 (Part 2)
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Day 1 (Part 1); Day 1 (Part 2)
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Time of the Maximum Measured Concentration (Tmax)
大体时间:Day 1 (Part 1); Day 1 (Part 2)
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Day 1 (Part 1); Day 1 (Part 2)
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Area Under the Concentration-Time Curve from Time Zero to the Last Quantifiable concentration-time point (AUClast)
大体时间:Day 1 (Part 1); Day 1 (Part 2)
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Day 1 (Part 1); Day 1 (Part 2)
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Area Under the Concentration-Time Curve from Time Zero Extrapolated to Infinity (AUCinf)
大体时间:Day 1 (Part 1); Day 1 (Part 2)
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Day 1 (Part 1); Day 1 (Part 2)
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Apparent Volume of Distribution at Steady State (Vz/F)
大体时间:Day 1 (Part 1)
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Day 1 (Part 1)
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Apparent Clearance (CL/F)
大体时间:Day 1 (Part 1)
|
Day 1 (Part 1)
|
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Terminal Elimination Half-Life (t½el)
大体时间:Day 1 (Part 1)
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Day 1 (Part 1)
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STAT6 biomarkers
大体时间:Day 1, Day 8,Day 15, Day 22,Day 29, Day 36, and Day 43 (Part 2)
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Day 1, Day 8,Day 15, Day 22,Day 29, Day 36, and Day 43 (Part 2)
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其他结果措施
结果测量 |
大体时间 |
|---|---|
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Change from Baseline in Eczema Area and Severity Index (EASI) Total Score
大体时间:Baseline and Week 4
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Baseline and Week 4
|
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Change from Baseline in Investigator's Global Assessment (IGA) Score
大体时间:Baseline and Week 4
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Baseline and Week 4
|
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Change from Baseline in Percentage of Body Surface Area (BSA) Affected by Atopic Dermatitis
大体时间:Baseline and Week 4
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Baseline and Week 4
|
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Change from Baseline in SCORing Atopic Dermatitis (SCORAD) Total Score
大体时间:Baseline and Week 4
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Baseline and Week 4
|
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Change from Baseline in Worst Itch Numerical Rating Scale (WI-NRS) Score
大体时间:Baseline and Week 4
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Baseline and Week 4
|
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Change from Baseline in Dermatology Life Quality Index (DLQI) Total Score
大体时间:Baseline and Week 4
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Baseline and Week 4
|
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Change from Baseline in Patient-Oriented Eczema Measure (POEM) Total Score
大体时间:Baseline and Week 4
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Baseline and Week 4
|
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Percentage of Participants Achieving EASI-50, EASI-75 or EASI-90
大体时间:Week 4
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Week 4
|
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Percentage of Participants With an IGA Score of 0 (Clear) or 1 (Almost Clear)
大体时间:Week 4
|
Week 4
|
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Percentage of Participants Achieving at Least a 4-Point Improvement in WI-NRS
大体时间:Week 4
|
Week 4
|
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Change from Baseline in Skin Biopsy Biomarker Assessments
大体时间:Baseline and Week 4
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Baseline and Week 4
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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 (实际的)
2026年9月14日
初级完成 (估计的)
2027年4月14日
研究完成 (估计的)
2027年5月19日
研究注册日期
首次提交
2026年8月26日
首先提交符合 QC 标准的
2026年8月29日
首次发布 (实际的)
2026年9月2日
研究记录更新
最后更新发布 (实际的)
2026年9月15日
上次提交的符合 QC 标准的更新
2026年9月13日
最后验证
2026年9月1日
更多信息
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.