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

2. November 2026 aktualisiert von: 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.

Studienübersicht

Status

Noch keine Rekrutierung

Bedingungen

Studientyp

Interventionell

Einschreibung (Geschätzt)

60

Phase

  • Phase 1

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

18 Jahre bis 75 Jahre (Erwachsene, Älterer Erwachsener)

Akzeptiert gesunde Freiwillige

Nein

Studienberechtigte Geschlechter

Alle

Beschreibung

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.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Doppelt

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: HSK60002 Dose 1 QD

HSK60002 tablets, oral administration.

Placebo tablets, oral administration.

Experimental: HSK60002 Dose 2 QD

HSK60002 tablets, oral administration.

Placebo tablets, oral administration.

Experimental: HSK60002 Dose 1 QW

HSK60002 tablets, oral administration.

Placebo tablets, oral administration.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Number of Participants With Treatment-Emergent Adverse Events (AEs), Serious Adverse Events (SAEs), and Adverse Events of Special Interest (AESI)
Zeitfenster: 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.

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Area Under the Plasma Concentration-Time Curve (AUC) of HSK60002
Zeitfenster: Day 1 to Day 127
Day 1 to Day 127
Maximum Observed Plasma Concentration (Cmax) of HSK60002
Zeitfenster: Day 1 to Day 127
Day 1 to Day 127
Time to Reach Maximum Plasma Concentration (Tmax) of HSK6000
Zeitfenster: Day 1 to Day 127
Day 1 to Day 127
Terminal Elimination Half-Life (t1/2) of HSK60002
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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.
Zeitfenster: 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
Zeitfenster: 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).
Zeitfenster: 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.
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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.
Zeitfenster: Baseline to Week 16 and follow-up
Baseline to Week 16 and follow-up
Change from baseline in serum Th2 biomarker(TARC).
Zeitfenster: Baseline to Week 16 and follow-up
Baseline to Week 16 and follow-up

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

1. November 2026

Primärer Abschluss (Geschätzt)

1. September 2027

Studienabschluss (Geschätzt)

1. Dezember 2027

Studienanmeldedaten

Zuerst eingereicht

16. Oktober 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

2. November 2026

Zuerst gepostet (Tatsächlich)

6. November 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

6. November 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

2. November 2026

Zuletzt verifiziert

1. November 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

NEIN

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

Produkt, das in den USA hergestellt und aus den USA exportiert wird

Nein

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

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