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A Study of HSK60002 Tablets in Participants With Moderate-to-Severe Atopic Dermatitis

2. listopadu 2026 aktualizováno: Haisco Pharmaceutical Group Co., Ltd.

A Phase Ib Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Preliminary Efficacy of HSK60002 Tablets in Participants With Moderate-to-Severe Atopic Dermatitis

This is a randomized, double-blind, placebo-controlled, Phase Ib study to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary efficacy of HSK60002 tablets in approximately 60 participants with moderate-to-severe atopic dermatitis (AD). Participants are randomized within one of three dose groups (10 mg once daily [QD], 30 mg QD, or 30 mg once weekly [QW]) in a 4:1 ratio to HSK60002 or matching placebo. Treatment is given orally for up to 16 weeks (Stage 1: Weeks 1-4; Stage 2: Weeks 5-16), followed by a safety follow-up visit approximately 2 weeks after the last dose.

Přehled studie

Postavení

Zatím nenabíráme

Podmínky

Intervence / Léčba

Typ studie

Intervenční

Zápis (Odhadovaný)

60

Fáze

  • Fáze 1

Kontakty a umístění

Tato část poskytuje kontaktní údaje pro ty, kteří studii provádějí, a informace o tom, kde se tato studie provádí.

Studijní kontakt

Kritéria účasti

Výzkumníci hledají lidi, kteří odpovídají určitému popisu, kterému se říká kritéria způsobilosti. Některé příklady těchto kritérií jsou celkový zdravotní stav osoby nebo předchozí léčba.

Kritéria způsobilosti

Věk způsobilý ke studiu

18 let až 75 let (Dospělý, Starší dospělý)

Přijímá zdravé dobrovolníky

Ne

Pohlaví způsobilá ke studiu

Všechno

Popis

Inclusion Criteria:

  • Capable of understanding and voluntarily providing informed consent before participating in any study-specific procedures.
  • Aged 18 to 75 years, inclusive, of any sex.
  • Able to understand and complete study-related questionnaires/scales, agree to photographic documentation of skin lesions, and comply with the visit schedule and other protocol requirements.
  • Diagnosed with atopic dermatitis according to the 2014 American Academy of Dermatology (AAD) criteria, with a history of AD or eczema for at least 6 months before screening, and stable AD disease, in the investigator's judgment, within 4 weeks before signing the informed consent form.
  • EASI score ≥16 at both screening and baseline visits.
  • vIGA-AD score ≥3 at both screening and baseline visits.
  • AD-involved body surface area (BSA) ≥10% at both screening and baseline visits.
  • Weekly average of daily Worst Itch Numeric Rating Scale (WI-NRS) score ≥4 at baseline.
  • In the investigator's judgment, inadequate clinical response to and/or intolerance of AD topical therapy within 6 months before screening, or disease controlled with systemic therapy.
  • Use of a stable dose of drug-free topical emollient applied twice daily for at least 7 consecutive days before the baseline visit, with continued use throughout the study.
  • Agreement to use highly effective contraception throughout the study.

Exclusion Criteria:

  • Any of the following treatments before the baseline visit: dupilumab or stapokibart (anti-IL-4Rα biologics) within 6 weeks; other known or potentially AD-affecting biologics within 12 weeks; systemic medications for AD within 4 weeks; topical AD therapy within 7 days; phototherapy for AD within 4 weeks.
  • Prior treatment with IL-4R- or IL-13-targeted biologics or JAK inhibitors with inadequate clinical response, in the investigator's judgment.
  • Administration of live attenuated vaccines within 12 weeks before baseline, or planned vaccination during the study.
  • Use of antihistamines within 1 week before baseline.
  • Allergen-specific immunotherapy within 6 months before baseline.
  • Use of any investigational product within 4 weeks or 5 half-lives before randomization, whichever is longer.
  • Clinically significant abnormal laboratory findings during screening.
  • Other active skin diseases or skin infections that may affect the assessment of AD treatment response, as assessed by the investigator.
  • Clinically significant chest X-ray or CT abnormality at screening.
  • Possible active Mycobacterium tuberculosis infection; history of TB infection or current TB infection.
  • History of invasive opportunistic infections.
  • Rheumatic fever, rheumatoid arthritis, systemic lupus erythematosus, dermatomyositis, multiple sclerosis, Sjögren's syndrome, inflammatory bowel disease, or other autoimmune diseases that may affect efficacy and safety assessment, as evaluated by the investigator.
  • Asthma requiring high-dose inhaled corticosteroids, systemic corticosteroids, or biologic therapy.
  • Major surgery within 3 months before screening or planned during the study.
  • Uncontrolled blood pressure despite antihypertensive treatment within 3 months before screening.
  • Thromboembolic events within 6 months before screening.
  • Uncontrolled clinically significant major medical conditions that would pose a safety risk, in the investigator's opinion.
  • History of malignancy within 5 years before screening.
  • History of atopic keratoconjunctivitis (AKC) involving the cornea, or history of vernal keratoconjunctivitis (VKC).
  • Dysphagia, gastrointestinal surgery, or severe gastrointestinal disease that may interfere with the pharmacokinetics of the study drug.
  • Active hepatitis B, positive hepatitis C antibody, syphilis infection, or HIV infection during screening.
  • History of drug abuse, illicit drug use, or alcohol abuse within 3 months before screening.
  • Use of any drugs that inhibit or induce hepatic drug-metabolizing enzymes within 28 days before the first dose of study drug.
  • Consumption of grapefruit (or grapefruit-containing products) within 48 hours before the first dose of study drug, or unwillingness to abstain during the study.
  • History of severe drug allergy or known allergy to the study drug or its excipients.
  • Pregnant or lactating women, or women planning pregnancy or lactation during the study.
  • Any other condition that, in the investigator's opinion, makes the participant unsuitable for the study.

Studijní plán

Tato část poskytuje podrobnosti o studijním plánu, včetně toho, jak je studie navržena a co studie měří.

Jak je studie koncipována?

Detaily designu

  • Primární účel: Léčba
  • Přidělení: Randomizované
  • Intervenční model: Paralelní přiřazení
  • Maskování: Dvojnásobek

Zbraně a zásahy

Skupina účastníků / Arm
Intervence / Léčba
Experimentální: HSK60002 Dose 1 QD

HSK60002 tablets, oral administration.

Placebo tablets, oral administration.

Experimentální: HSK60002 Dose 2 QD

HSK60002 tablets, oral administration.

Placebo tablets, oral administration.

Experimentální: HSK60002 Dose 1 QW

HSK60002 tablets, oral administration.

Placebo tablets, oral administration.

Co je měření studie?

Primární výstupní opatření

Měření výsledku
Popis opatření
Časové okno
Number of Participants With Treatment-Emergent Adverse Events (AEs), Serious Adverse Events (SAEs), and Adverse Events of Special Interest (AESI)
Časové okno: From first dose (Day 1) through Week 16 (end of treatment) and the safety follow-up visit approximately 2 weeks after the last dose.

Safety and tolerability of HSK60002 tablets assessed by the incidence and severity of AEs, SAEs, and AESI, clinical laboratory tests (hematology, blood chemistry, urinalysis), 12-lead ECG, T-SPOT.TB test, chest X-ray or CT, vital signs, and physical examination.

From first dose (Day 1) through Week 16 (end of treatment) and the safety follow-up visit approximately 2 weeks after the last dose.

Sekundární výstupní opatření

Měření výsledku
Popis opatření
Časové okno
Area Under the Plasma Concentration-Time Curve (AUC) of HSK60002
Časové okno: Day 1 to Day 127
Day 1 to Day 127
Maximum Observed Plasma Concentration (Cmax) of HSK60002
Časové okno: Day 1 to Day 127
Day 1 to Day 127
Time to Reach Maximum Plasma Concentration (Tmax) of HSK6000
Časové okno: Day 1 to Day 127
Day 1 to Day 127
Terminal Elimination Half-Life (t1/2) of HSK60002
Časové okno: Day 1 to Day 127
Day 1 to Day 127
Proportion of Participants Achieving at Least a 75% Improvement From Baseline in Eczema Area and Severity Index (EASI-75) at Week 16
Časové okno: Baseline (Day -1) to Week 16

The Eczema Area and Severity Index (EASI) is a composite measure of the extent and severity of atopic dermatitis, with total scores ranging from 0 (no disease) to 72 (most severe disease); higher scores indicate more severe disease. EASI-75 is defined as at least a 75% improvement (reduction) in EASI score from baseline.

Baseline (Day -1) to Week 16
Proportion of Participants Achieving at Least a 50% Improvement From Baseline in Eczema Area and Severity Index (EASI-50) at Week 16
Časové okno: Baseline to Week 16

The Eczema Area and Severity Index (EASI) is a composite measure of the extent and severity of atopic dermatitis, with total scores ranging from 0 (no disease) to 72 (most severe disease); higher scores indicate more severe disease. EASI-50 is defined as at least a 50% improvement (reduction) in EASI score from baseline.

Baseline to Week 16
Proportion of participants achieving a validated Investigator's Global Assessment for Atopic Dermatitis (vIGA-AD) score of 0 or 1 with a reduction of ≥2 points from baseline.
Časové okno: Baseline to Week 16 and follow-up

The validated Investigator's Global Assessment for Atopic Dermatitis (vIGA-AD) is a 5-point scale ranging from 0 (clear) to 4 (severe), with higher scores indicating more severe disease. Treatment success is defined as a score of 0 (clear) or 1 (almost clear) with at least a 2-point reduction from baseline.

Baseline to Week 16 and follow-up
Change from baseline in weekly average of daily Worst Itch Numeric Rating Scale (WI-NRS) score
Časové okno: Baseline to Week 16 and follow-up

The Worst Itch Numeric Rating Scale (WI-NRS) is an 11-point scale ranging from 0 (no itch) to 10 (worst imaginable itch), with higher scores indicating worse itch severity

Baseline to Week 16 and follow-up
Change from baseline in percentage of body surface area (BSA) affected by Atopic Dermatitis (AD).
Časové okno: Baseline to Week 16 and follow-up

The percentage of body surface area (BSA) affected by atopic dermatitis ranges from 0% (no involvement) to 100% (full-body involvement), with higher percentages indicating greater extent of disease.

Baseline to Week 16 and follow-up
Change from baseline in SCORing Atopic Dermatitis (SCORAD) score.
Časové okno: Baseline to Week 16 and follow-up

The SCORing Atopic Dermatitis (SCORAD) index is a composite measure of disease extent, intensity, and subjective symptoms (itch and sleep loss). Total scores range from 0 (no disease) to 103 (most severe disease), with higher scores indicating more severe atopic dermatitis.

Baseline to Week 16 and follow-up
Change From Baseline in Patient-Oriented Eczema Measure (POEM) Score
Časové okno: Baseline to Week 16 and follow-up

The Patient-Oriented Eczema Measure (POEM) is a 7-item patient-reported questionnaire assessing symptoms of atopic dermatitis (itch, sleep disturbance, dryness, flaking, cracking, bleeding, and oozing/weeping) over the previous week. Total scores range from 0 (no symptoms) to 28 (most severe symptoms), with higher scores indicating more severe disease.

Baseline to Week 16 and follow-up
Change From Baseline in Dermatology Life Quality Index (DLQI) Score
Časové okno: Baseline to Week 16 and follow-up

The Dermatology Life Quality Index (DLQI) is a 10-item patient-reported questionnaire assessing the impact of skin disease on quality of life over the previous week, covering symptoms and feelings, daily activities, leisure, work and school, personal relationships, and treatment burden. Total scores range from 0 (no impact) to 30 (maximum impact), with higher scores indicating greater impairment of quality of life.

Baseline to Week 16 and follow-up
STAT6 protein levels in whole blood and skin tissue and change from baseline.
Časové okno: Baseline to Week 16 and follow-up
Baseline to Week 16 and follow-up
Change from baseline in serum Th2 biomarker(TARC).
Časové okno: Baseline to Week 16 and follow-up
Baseline to Week 16 and follow-up

Spolupracovníci a vyšetřovatelé

Zde najdete lidi a organizace zapojené do této studie.

Sponzor

Termíny studijních záznamů

Tato data sledují průběh záznamů studie a předkládání souhrnných výsledků na ClinicalTrials.gov. Záznamy ze studií a hlášené výsledky jsou před zveřejněním na veřejné webové stránce přezkoumány Národní lékařskou knihovnou (NLM), aby se ujistily, že splňují specifické standardy kontroly kvality.

Hlavní termíny studia

Začátek studia (Odhadovaný)

1. listopadu 2026

Primární dokončení (Odhadovaný)

1. září 2027

Dokončení studie (Odhadovaný)

1. prosince 2027

Termíny zápisu do studia

První předloženo

16. října 2026

První předloženo, které splnilo kritéria kontroly kvality

2. listopadu 2026

První zveřejněno (Aktuální)

6. listopadu 2026

Aktualizace studijních záznamů

Poslední zveřejněná aktualizace (Aktuální)

6. listopadu 2026

Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality

2. listopadu 2026

Naposledy ověřeno

1. listopadu 2026

Více informací

Termíny související s touto studií

Další identifikační čísla studie

  • HSK60002-104

Plán pro data jednotlivých účastníků (IPD)

Plánujete sdílet data jednotlivých účastníků (IPD)?

NE

Informace o lécích a zařízeních, studijní dokumenty

Studuje lékový produkt regulovaný americkým FDA

Ne

Studuje produkt zařízení regulovaný americkým úřadem FDA

Ne

produkt vyrobený a vyvážený z USA

Ne

Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .