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.
調査の概要
研究の種類
介入
入学 (推定)
84
段階
- フェーズ 1
連絡先と場所
このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。
研究連絡先
- 名前:Yan Liu
- 電話番号:+86 18782948571
- メール:yan.liu16@tigermedgrp.com
研究場所
-
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Shanghai Municipality
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Shanghai、Shanghai Municipality、中国、200040
- 募集
- Huashan Hospital, Fudan University
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主任研究者:
- Jing Zhang
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主任研究者:
- Wenyu Wu
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コンタクト:
- Jing Zhang
- 電話番号:021-52887976
- メール:Zhangj_fudan@163.com
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-
参加基準
研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。
適格基準
就学可能な年齢
- 子
- 大人
- 高齢者
健康ボランティアの受け入れ
はい
説明
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;
研究計画
このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:4倍
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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実験的:QX4533
oral tablets administered once daily
|
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
|
|
プラセボコンパレーター: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
|
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Incidence of Treatment-emergent Adverse Events (TEAEs)
時間枠: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
時間枠: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])
|
二次結果の測定
結果測定 |
時間枠 |
|---|---|
|
Maximum Observed Plasma Concentration (Cmax)
時間枠:Day 1 (Part 1); Day 1 (Part 2)
|
Day 1 (Part 1); Day 1 (Part 2)
|
|
Time of the Maximum Measured Concentration (Tmax)
時間枠:Day 1 (Part 1); Day 1 (Part 2)
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Day 1 (Part 1); Day 1 (Part 2)
|
|
Area Under the Concentration-Time Curve from Time Zero to the Last Quantifiable concentration-time point (AUClast)
時間枠:Day 1 (Part 1); Day 1 (Part 2)
|
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)
時間枠:Day 1 (Part 1); Day 1 (Part 2)
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Day 1 (Part 1); Day 1 (Part 2)
|
|
Apparent Volume of Distribution at Steady State (Vz/F)
時間枠:Day 1 (Part 1)
|
Day 1 (Part 1)
|
|
Apparent Clearance (CL/F)
時間枠:Day 1 (Part 1)
|
Day 1 (Part 1)
|
|
Terminal Elimination Half-Life (t½el)
時間枠:Day 1 (Part 1)
|
Day 1 (Part 1)
|
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STAT6 biomarkers
時間枠: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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その他の成果指標
結果測定 |
時間枠 |
|---|---|
|
Change from Baseline in Eczema Area and Severity Index (EASI) Total Score
時間枠: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
時間枠: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
時間枠:Baseline and Week 4
|
Baseline and Week 4
|
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Change from Baseline in SCORing Atopic Dermatitis (SCORAD) Total Score
時間枠:Baseline and Week 4
|
Baseline and Week 4
|
|
Change from Baseline in Worst Itch Numerical Rating Scale (WI-NRS) Score
時間枠:Baseline and Week 4
|
Baseline and Week 4
|
|
Change from Baseline in Dermatology Life Quality Index (DLQI) Total Score
時間枠:Baseline and Week 4
|
Baseline and Week 4
|
|
Change from Baseline in Patient-Oriented Eczema Measure (POEM) Total Score
時間枠:Baseline and Week 4
|
Baseline and Week 4
|
|
Percentage of Participants Achieving EASI-50, EASI-75 or EASI-90
時間枠:Week 4
|
Week 4
|
|
Percentage of Participants With an IGA Score of 0 (Clear) or 1 (Almost Clear)
時間枠:Week 4
|
Week 4
|
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Percentage of Participants Achieving at Least a 4-Point Improvement in WI-NRS
時間枠:Week 4
|
Week 4
|
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Change from Baseline in Skin Biopsy Biomarker Assessments
時間枠:Baseline and Week 4
|
Baseline and Week 4
|
協力者と研究者
ここでは、この調査に関係する人々や組織を見つけることができます。
スポンサー
研究記録日
これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。
主要日程の研究
研究開始 (実際)
2026年9月14日
一次修了 (推定)
2027年4月14日
研究の完了 (推定)
2027年5月19日
試験登録日
最初に提出
2026年8月26日
QC基準を満たした最初の提出物
2026年8月29日
最初の投稿 (実際)
2026年9月2日
学習記録の更新
投稿された最後の更新 (実際)
2026年9月15日
QC基準を満たした最後の更新が送信されました
2026年9月13日
最終確認日
2026年9月1日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
- QX4533-002
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
未定
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
いいえ
米国FDA規制機器製品の研究
いいえ
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。