Deze pagina is automatisch vertaald en de nauwkeurigheid van de vertaling kan niet worden gegarandeerd. Raadpleeg de Engelse versie voor een brontekst.

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

13 september 2026 bijgewerkt door: 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.

Studie Overzicht

Toestand

Werving

Studietype

Ingrijpend

Inschrijving (Geschat)

84

Fase

  • Fase 1

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studiecontact

Studie Locaties

    • Shanghai Municipality
      • Shanghai, Shanghai Municipality, China, 200040
        • Werving
        • Huashan Hospital, Fudan University
        • Hoofdonderzoeker:
          • Jing Zhang
        • Hoofdonderzoeker:
          • Wenyu Wu
        • Contact:

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Kind
  • Volwassen
  • Oudere volwassene

Accepteert gezonde vrijwilligers

Ja

Beschrijving

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;

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Verviervoudigen

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: 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
Placebo-vergelijker: 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

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Incidence of Treatment-emergent Adverse Events (TEAEs)
Tijdsspanne: 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
Tijdsspanne: 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])

Secundaire uitkomstmaten

Uitkomstmaat
Tijdsspanne
Maximum Observed Plasma Concentration (Cmax)
Tijdsspanne: Day 1 (Part 1); Day 1 (Part 2)
Day 1 (Part 1); Day 1 (Part 2)
Time of the Maximum Measured Concentration (Tmax)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: Day 1 (Part 1)
Day 1 (Part 1)
Apparent Clearance (CL/F)
Tijdsspanne: Day 1 (Part 1)
Day 1 (Part 1)
Terminal Elimination Half-Life (t½el)
Tijdsspanne: Day 1 (Part 1)
Day 1 (Part 1)
STAT6 biomarkers
Tijdsspanne: 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)

Andere uitkomstmaten

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

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

14 september 2026

Primaire voltooiing (Geschat)

14 april 2027

Studie voltooiing (Geschat)

19 mei 2027

Studieregistratiedata

Eerst ingediend

26 augustus 2026

Eerst ingediend dat voldeed aan de QC-criteria

29 augustus 2026

Eerst geplaatst (Werkelijk)

2 september 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

15 september 2026

Laatste update ingediend die voldeed aan QC-criteria

13 september 2026

Laatst geverifieerd

1 september 2026

Meer informatie

Termen gerelateerd aan deze studie

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

ONBESLIST

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

Abonneren