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RecruitingNCT07800104Updated Sep 15, 2026

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

A Phase 1 interventional study of QX4533 and QX4533 Placebo in Atopic Dermatitis, sponsored by QuantX Biosciences, Inc.. Recruiting at 1 site in China. Open to participants aged 18 Months to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-15.

Sponsored by QuantX Biosciences, Inc. · Phase 1, Interventional, and Treatment

Phase
Phase 1
Study type
Interventional
Enrollment
84
Allocation
Randomized
Ages
18 Months to 65 Years
Sex
All
01

Study summary

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.

02

Conditions studied

  • Atopic Dermatitis

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03

Who can participate

Ages eligible
18 Months to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Eligibility criteria

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;
04

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
84 participants (estimated)

Study arms

  • Experimental
    QX4533

    oral tablets administered once daily

    Drug: QX4533

  • Placebo comparator
    QX4533 Placebo

    oral tablets administered once daily

    Drug: QX4533 Placebo

Interventions

  • DrugQX4533

    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

  • DrugQX4533 Placebo

    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

05

What researchers measure

Primary outcomes

  1. Incidence of Treatment-emergent Adverse Events (TEAEs)

    Number of Participants with Treatment-emergent Adverse Events (TEAEs)

    Time frame: From enrollment through the safety follow-up visit (up to Day 9 [Part 1] and Day 43 [Part 2])

  2. Number of Participants with Clinically Significant Laboratory Parameter Changes

    Number of Participants with Clinically Significant Change from Baseline in Clinical Laboratory Parameters

    Time frame: From enrollment through the safety follow-up visit (up to Day 9 [Part 1] and Day 43 [Part 2])

Secondary outcomes

  1. Maximum Observed Plasma Concentration (Cmax)

    Time frame: Day 1 (Part 1); Day 1 (Part 2)

  2. Time of the Maximum Measured Concentration (Tmax)

    Time frame: Day 1 (Part 1); Day 1 (Part 2)

  3. Area Under the Concentration-Time Curve from Time Zero to the Last Quantifiable concentration-time point (AUClast)

    Time frame: Day 1 (Part 1); Day 1 (Part 2)

  4. Area Under the Concentration-Time Curve from Time Zero Extrapolated to Infinity (AUCinf)

    Time frame: Day 1 (Part 1); Day 1 (Part 2)

  5. Apparent Volume of Distribution at Steady State (Vz/F)

    Time frame: Day 1 (Part 1)

  6. Apparent Clearance (CL/F)

    Time frame: Day 1 (Part 1)

  7. Terminal Elimination Half-Life (t½el)

    Time frame: Day 1 (Part 1)

  8. STAT6 biomarkers

    Time frame: Day 1, Day 8,Day 15, Day 22,Day 29, Day 36, and Day 43 (Part 2)

Other outcomes

  1. Change from Baseline in Eczema Area and Severity Index (EASI) Total Score

    Time frame: Baseline and Week 4

  2. Change from Baseline in Investigator's Global Assessment (IGA) Score

    Time frame: Baseline and Week 4

  3. Change from Baseline in Percentage of Body Surface Area (BSA) Affected by Atopic Dermatitis

    Time frame: Baseline and Week 4

  4. Change from Baseline in SCORing Atopic Dermatitis (SCORAD) Total Score

    Time frame: Baseline and Week 4

  5. Change from Baseline in Worst Itch Numerical Rating Scale (WI-NRS) Score

    Time frame: Baseline and Week 4

  6. Change from Baseline in Dermatology Life Quality Index (DLQI) Total Score

    Time frame: Baseline and Week 4

  7. Change from Baseline in Patient-Oriented Eczema Measure (POEM) Total Score

    Time frame: Baseline and Week 4

  8. Percentage of Participants Achieving EASI-50, EASI-75 or EASI-90

    Time frame: Week 4

  9. Percentage of Participants With an IGA Score of 0 (Clear) or 1 (Almost Clear)

    Time frame: Week 4

  10. Percentage of Participants Achieving at Least a 4-Point Improvement in WI-NRS

    Time frame: Week 4

  11. Change from Baseline in Skin Biopsy Biomarker Assessments

    Time frame: Baseline and Week 4

06

Study locations

1 of 1 sites recruiting
  • Huashan Hospital, Fudan University
    Shanghai, Shanghai Municipality 200040, China
    • Jing Zhang · Contact · Zhangj_fudan@163.com · 021-52887976
    • Wenyu Wu · Principal investigator
    • Jing Zhang · Principal investigator
    Recruiting
07

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT07800104
Lead sponsor
QuantX Biosciences, Inc.
Responsible party
Sponsor
First posted
Sep 2, 2026
Start date
Sep 14, 2026
Primary completion
Apr 14, 2027 (estimated)
Completion
May 19, 2027 (estimated)
Last update
Sep 15, 2026

Study contacts

Yan Liu
Contact
yan.liu16@tigermedgrp.com
+86 18782948571

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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