- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07800104
Phase 1 Study of QX-4533 in Healthy Volunteers and Patients With Moderate-to-Severe Atopic Dermatitis
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
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Tipo di studio
Iscrizione (Stimato)
Fase
- Fase 1
Contatti e Sedi
Contatto studio
- Nome: Yan Liu
- Numero di telefono: +86 18782948571
- Email: yan.liu16@tigermedgrp.com
Luoghi di studio
-
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Shanghai Municipality
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Shanghai, Shanghai Municipality, Cina, 200040
- Reclutamento
- Huashan Hospital, Fudan University
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Investigatore principale:
- Jing Zhang
-
Investigatore principale:
- Wenyu Wu
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Contatto:
- Jing Zhang
- Numero di telefono: 021-52887976
- Email: Zhangj_fudan@163.com
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-
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
- Bambino
- Adulto
- Adulto più anziano
Accetta volontari sani
Descrizione
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;
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Quadruplicare
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
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Sperimentale: 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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Comparatore placebo: 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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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Incidence of Treatment-emergent Adverse Events (TEAEs)
Lasso di tempo: 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
Lasso di tempo: 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
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From enrollment through the safety follow-up visit (up to Day 9 [Part 1] and Day 43 [Part 2])
|
Misure di risultato secondarie
Misura del risultato |
Lasso di tempo |
|---|---|
|
Maximum Observed Plasma Concentration (Cmax)
Lasso di tempo: Day 1 (Part 1); Day 1 (Part 2)
|
Day 1 (Part 1); Day 1 (Part 2)
|
|
Time of the Maximum Measured Concentration (Tmax)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: Day 1 (Part 1)
|
Day 1 (Part 1)
|
|
Apparent Clearance (CL/F)
Lasso di tempo: Day 1 (Part 1)
|
Day 1 (Part 1)
|
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Terminal Elimination Half-Life (t½el)
Lasso di tempo: Day 1 (Part 1)
|
Day 1 (Part 1)
|
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STAT6 biomarkers
Lasso di tempo: 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)
|
Altre misure di risultato
Misura del risultato |
Lasso di tempo |
|---|---|
|
Change from Baseline in Eczema Area and Severity Index (EASI) Total Score
Lasso di tempo: Baseline and Week 4
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Baseline and Week 4
|
|
Change from Baseline in Investigator's Global Assessment (IGA) Score
Lasso di tempo: Baseline and Week 4
|
Baseline and Week 4
|
|
Change from Baseline in Percentage of Body Surface Area (BSA) Affected by Atopic Dermatitis
Lasso di tempo: Baseline and Week 4
|
Baseline and Week 4
|
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Change from Baseline in SCORing Atopic Dermatitis (SCORAD) Total Score
Lasso di tempo: Baseline and Week 4
|
Baseline and Week 4
|
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Change from Baseline in Worst Itch Numerical Rating Scale (WI-NRS) Score
Lasso di tempo: Baseline and Week 4
|
Baseline and Week 4
|
|
Change from Baseline in Dermatology Life Quality Index (DLQI) Total Score
Lasso di tempo: Baseline and Week 4
|
Baseline and Week 4
|
|
Change from Baseline in Patient-Oriented Eczema Measure (POEM) Total Score
Lasso di tempo: Baseline and Week 4
|
Baseline and Week 4
|
|
Percentage of Participants Achieving EASI-50, EASI-75 or EASI-90
Lasso di tempo: Week 4
|
Week 4
|
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Percentage of Participants With an IGA Score of 0 (Clear) or 1 (Almost Clear)
Lasso di tempo: Week 4
|
Week 4
|
|
Percentage of Participants Achieving at Least a 4-Point Improvement in WI-NRS
Lasso di tempo: Week 4
|
Week 4
|
|
Change from Baseline in Skin Biopsy Biomarker Assessments
Lasso di tempo: Baseline and Week 4
|
Baseline and Week 4
|
Collaboratori e investigatori
Sponsor
Studiare le date dei record
Studia le date principali
Inizio studio (Effettivo)
Completamento primario (Stimato)
Completamento dello studio (Stimato)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
- Malattie genetiche, congenite
- Malattie del sistema immunitario
- Ipersensibilità, immediata
- Ipersensibilità
- Malattie della pelle
- Malattie della pelle, genetiche
- Malattie della pelle, eczematose
- Dermatite
- Malattie e anomalie congenite, ereditarie e neonatali
- Malattie della pelle e del tessuto connettivo
- Dermatite, atopica
Altri numeri di identificazione dello studio
- QX4533-002
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
Informazioni su farmaci e dispositivi, documenti di studio
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Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .