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Phase 1 Study of QX-4533 in Healthy Volunteers and Patients With Moderate-to-Severe Atopic Dermatitis

13 septembre 2026 mis à jour par: 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.

Aperçu de l'étude

Statut

Recrutement

Les conditions

Type d'étude

Interventionnel

Inscription (Estimé)

84

Phase

  • La phase 1

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Lieux d'étude

    • Shanghai Municipality
      • Shanghai, Shanghai Municipality, Chine, 200040
        • Recrutement
        • Huashan Hospital, Fudan University
        • Chercheur principal:
          • Jing Zhang
        • Chercheur principal:
          • Wenyu Wu
        • Contact:

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Enfant
  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Oui

La description

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:

  1. Fully understanding the purpose, nature, method, and possible adverse reactions of the trial, voluntarily participating as a clinical trial participant, and signing the ICF;
  2. Being willing and able to comply with the study protocol and cooperate in completing the visit procedures throughout the study;
  3. Males and females aged 18 to 55 years (inclusive, at the time of signing the ICF) at screening;
  4. Body mass index (BMI) of 18 to 28 kg/m2 (inclusive); weight not less than 50 kg for male and 45 kg for female;
  5. 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;
  6. 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:

  1. Fully understanding the purpose, nature, method, and possible adverse reactions of the trial, voluntarily participating as a participant, and signing the ICF;
  2. 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;
  3. Males and females aged 18 to 65 years (inclusive) at screening;
  4. 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;
  5. Participants with inadequate response, intolerance, or contraindication to topical corticosteroids and/or topical calcineurin inhibitors;
  6. 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;
  7. 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:

  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;
  2. 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;
  3. 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);
  4. Participants with a history of any ongoing medical condition requiring treatment with prescription medication within two weeks prior to screening;
  5. Participants with a history of any infection requiring treatment with a prescription anti-infective in the past 4 weeks prior to screening;
  6. 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;
  7. Participants with history of malignancy, except fully resolved basal cell carcinoma (BCC), squamous cell carcinoma (SCC), or in situ carcinoma of the uterine cervix;
  8. 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;
  9. 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;
  10. 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;
  11. 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;
  12. 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;
  13. 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;
  14. 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;
  15. 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:

  1. 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;
  2. Planned major surgical procedure during the length of the study;
  3. 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;

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Quadruple

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: 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
Comparateur placebo: QX4533 Placebo
oral tablets administered once daily
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

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Incidence of Treatment-emergent Adverse Events (TEAEs)
Délai: From enrollment through the safety follow-up visit (up to Day 9 [Part 1] and Day 43 [Part 2])
Number of Participants with Treatment-emergent Adverse Events (TEAEs)
From enrollment through the safety follow-up visit (up to Day 9 [Part 1] and Day 43 [Part 2])
Number of Participants with Clinically Significant Laboratory Parameter Changes
Délai: From enrollment through the safety follow-up visit (up to Day 9 [Part 1] and Day 43 [Part 2])
Number of Participants with Clinically Significant Change from Baseline in Clinical Laboratory Parameters
From enrollment through the safety follow-up visit (up to Day 9 [Part 1] and Day 43 [Part 2])

Mesures de résultats secondaires

Mesure des résultats
Délai
Maximum Observed Plasma Concentration (Cmax)
Délai: Day 1 (Part 1); Day 1 (Part 2)
Day 1 (Part 1); Day 1 (Part 2)
Time of the Maximum Measured Concentration (Tmax)
Délai: Day 1 (Part 1); Day 1 (Part 2)
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)
Délai: Day 1 (Part 1); Day 1 (Part 2)
Day 1 (Part 1); Day 1 (Part 2)
Area Under the Concentration-Time Curve from Time Zero Extrapolated to Infinity (AUCinf)
Délai: Day 1 (Part 1); Day 1 (Part 2)
Day 1 (Part 1); Day 1 (Part 2)
Apparent Volume of Distribution at Steady State (Vz/F)
Délai: Day 1 (Part 1)
Day 1 (Part 1)
Apparent Clearance (CL/F)
Délai: Day 1 (Part 1)
Day 1 (Part 1)
Terminal Elimination Half-Life (t½el)
Délai: Day 1 (Part 1)
Day 1 (Part 1)
STAT6 biomarkers
Délai: Day 1, Day 8,Day 15, Day 22,Day 29, Day 36, and Day 43 (Part 2)
Day 1, Day 8,Day 15, Day 22,Day 29, Day 36, and Day 43 (Part 2)

Autres mesures de résultats

Mesure des résultats
Délai
Change from Baseline in Eczema Area and Severity Index (EASI) Total Score
Délai: Baseline and Week 4
Baseline and Week 4
Change from Baseline in Investigator's Global Assessment (IGA) Score
Délai: Baseline and Week 4
Baseline and Week 4
Change from Baseline in Percentage of Body Surface Area (BSA) Affected by Atopic Dermatitis
Délai: Baseline and Week 4
Baseline and Week 4
Change from Baseline in SCORing Atopic Dermatitis (SCORAD) Total Score
Délai: Baseline and Week 4
Baseline and Week 4
Change from Baseline in Worst Itch Numerical Rating Scale (WI-NRS) Score
Délai: Baseline and Week 4
Baseline and Week 4
Change from Baseline in Dermatology Life Quality Index (DLQI) Total Score
Délai: Baseline and Week 4
Baseline and Week 4
Change from Baseline in Patient-Oriented Eczema Measure (POEM) Total Score
Délai: Baseline and Week 4
Baseline and Week 4
Percentage of Participants Achieving EASI-50, EASI-75 or EASI-90
Délai: Week 4
Week 4
Percentage of Participants With an IGA Score of 0 (Clear) or 1 (Almost Clear)
Délai: Week 4
Week 4
Percentage of Participants Achieving at Least a 4-Point Improvement in WI-NRS
Délai: Week 4
Week 4
Change from Baseline in Skin Biopsy Biomarker Assessments
Délai: Baseline and Week 4
Baseline and Week 4

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

14 septembre 2026

Achèvement primaire (Estimé)

14 avril 2027

Achèvement de l'étude (Estimé)

19 mai 2027

Dates d'inscription aux études

Première soumission

26 août 2026

Première soumission répondant aux critères de contrôle qualité

29 août 2026

Première publication (Réel)

2 septembre 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

15 septembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

13 septembre 2026

Dernière vérification

1 septembre 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

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INDÉCIS

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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