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A Study to Evaluate the Efficacy, Safety, and Pharmacokinetic Profiles of TLL-018 in Patients With Moderate-to-Severe Atopic Dermatitis

21. August 2026 aktualisiert von: Hangzhou Highlightll Pharmaceutical Co., Ltd

A Phase II/III, Multicenter, Randomized, Double-Blind, Placebo-Controlled Clinical Study to Evaluate the Efficacy, Safety, and Pharmacokinetic Profiles of TLL-018 in Patients With Moderate-to-Severe Atopic Dermatitis

This is an operationally seamless Phase II/III, multicenter, randomized, double-blind, placebo-controlled trial in patients with moderate-to-severe atopic dermatitis (AD). The Phase II stage aims to preliminarily evaluate the efficacy of TLL-018 and identify the dose and sample size for the subsequent Phase III stage, which is designed to confirm the efficacy of TLL-018.

The primary outcome measures are the proportion of participants achieving EASI-75 (≥75% improvement in Eczema Area and Severity Index from baseline) at week 16, and the proportion of participants achieving an Investigator's Global Assessment (IGA) score of 0 or 1 with a ≥2-point reduction from baseline at week 16.

Studienübersicht

Status

Noch keine Rekrutierung

Bedingungen

Intervention / Behandlung

Studientyp

Interventionell

Einschreibung (Geschätzt)

390

Phase

  • Phase 2
  • Phase 3

Kontakte und Standorte

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

Studienorte

      • Beijing, China, 100044
        • Peking University People's Hospital
        • Kontakt:
          • Jianzhong Zhang, MD
          • Telefonnummer: 86-10- 88325472
          • E-Mail: rmzjz@126.com
        • Kontakt:
          • Cheng Zhou, MD

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

  • Erwachsene
  • Älterer Erwachsener

Akzeptiert gesunde Freiwillige

Nein

Beschreibung

Inclusion Criteria:

  • The trial participant understands and voluntarily signs the informed consent form (ICF), and has the willingness and ability to complete the scheduled follow-up visits, treatment plans, laboratory tests, and other trial procedures required by the protocol.
  • Male or female trial participants aged ≥18 and ≤75 years at the time of signing the ICF.
  • Have a history of atopic dermatitis for at least 1 year at screening, and meet the Hanifin-Rajka diagnostic criteria.
  • At screening and randomization, meet the criteria for moderate-to-severe atopic dermatitis as assessed by the investigator, with all of the following 4 conditions met simultaneously: Eczema Area and Severity Index (EASI) ≥16; Investigator's Global Assessment (IGA) ≥3; Body Surface Area (BSA) affected by atopic dermatitis ≥10%; Weekly average of Worst Itch Numeric Rating Scale (WI-NRS) ≥4.

    5. In the investigator's judgment, have received topical treatment for atopic dermatitis within 6 months prior to screening with inadequate clinical response or intolerance, or require systemic therapy to control the disease.

    6. The trial participant is able and willing to regularly use a mild emollient without active ingredients twice daily for at least 7 consecutive days prior to randomization, and to continue using it throughout the study.

    7. Female trial participants of childbearing potential must not be pregnant or lactating, and may enter the study only after pregnancy test results are confirmed negative.

    8. Female trial participants of childbearing potential, male trial participants, and their partners must use adequate and effective contraceptive measures from the screening period until 90 days after the last dose, and must have no plans to donate sperm (males) or ova (females) from the screening period until at least 6 months after the last dose.

Exclusion Criteria:

  • Presence of any of the following diseases or medical histories:

    1. Inability to swallow investigational product, refractory nausea/vomiting, malabsorption, external biliary diversion; history of gastrointestinal perforation (excluding perforation secondary to appendicitis or mechanical trauma); gastrointestinal disorders impairing drug absorption or other malabsorption conditions.
    2. Concurrent active inflammatory skin diseases that may confound efficacy assessment.
    3. Current or prior lymphoproliferative disorders, or suggestive signs/symptoms including lymphadenopathy or splenomegaly.
    4. History of malignancy prior to screening, except for treated-and-cured non-melanoma skin cancer/basal-cell carcinoma, cervical carcinoma in-situ, or breast ductal carcinoma in-situ.
    5. Herpes zoster within 1 year before randomization; any prior disseminated or recurrent herpes zoster; any prior disseminated herpes simplex.
    6. Severe/systemic infections within 4 weeks pre-randomization requiring intravenous anti-infective therapy or resulting in infection-related hospitalization; or other active/recent infections judged by the investigator to confer unacceptable subject risk.
    7. Acquired or hereditary immunodeficiency disorders.
    8. Severe haematological diseases, or conditions predisposing to haemolysis or red-cell instability.
    9. Documented psychiatric disorders likely to impair trial compliance, or known poor adherence.
    10. Major surgery or severe trauma within 4 weeks pre-randomization, or planned major surgery during the trial.
    11. Prior or planned solid-organ transplantation (e.g., liver transplantation).
    12. History or evidence of high-risk cardiovascular/cerebrovascular disease.
  • Any screening laboratory abnormality meeting the following thresholds:

    1. Complete blood count: haemoglobin < 90 g/L; white-blood-cell count < 2.5 × 10⁹/L; absolute-neutrophil count < 1.5 × 10⁹/L; lymphocyte count < 0.8 × 10⁹/L; platelet count < 100 × 10⁹/L.
    2. Liver function: AST or ALT > 2 × upper-limit-of-normal (ULN); total bilirubin > 2 × ULN.
    3. Serum creatinine ≥ 1.2 × ULN.
    4. Coagulation: PT or APTT > ULN with clinical significance.
    5. Uncontrolled hypertension: SBP ≥ 160 mmHg and/or DBP ≥ 100 mmHg. Confirmatory measurement: if initial reading exceeds threshold, rest ≥ 5 minutes then re-measure once; use repeat value if below threshold.
    6. Uncontrolled dyslipidaemia: fasting total cholesterol ≥ 7.2 mmol/L, or fasting LDL-C ≥ 4.9 mmol/L, or fasting triglycerides > 5.6 mmol/L.
  • Tuberculosis-related exclusion criteria:

    1. History of active TB without documented clinical cure.
    2. Screening imaging (e.g., chest-CT) demonstrating active TB.
    3. Suspicious TB-related symptoms that cannot be ruled out by investigator (low-grade fever, cough, night-sweats, weight loss etc.).
    4. Latent tuberculosis infection (LTBI): positive TB assay (T-SPOT-TB, QuantiFERON-TB-Gold etc.) without active-TB signs/symptoms.
  • Progressive/uncontrolled renal, hepatic, haematological, gastrointestinal, endocrine, pulmonary, cardiovascular, neurological, psychiatric or cerebral disease; investigator judges participation poses unacceptable risk.
  • Known or suspected hypersensitivity to TLL-018 active substance, excipients, or agents of the same drug class.

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: Vervierfachen

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Arm A
TLL-018 10 mg. Dose selection for continuation into Stage 2 (Phase III) will be based on efficacy and safety data generated from Stage 1 (Phase II). This dose group may or may not be carried forward into Stage 2.
TLL-018 tablets taken orally 10 mg (1 tablet) twice daily
TLL-018 tablets taken orally 20 mg (2 tablets) twice daily
TLL-018 tablets taken orally 30 mg (3 tablets) twice daily
Experimental: Arm B
TLL-018 20 mg. Dose selection for continuation into Stage 2 (Phase III) will be based on efficacy and safety data generated from Stage 1 (Phase II). This dose group may or may not be carried forward into Stage 2.
TLL-018 tablets taken orally 10 mg (1 tablet) twice daily
TLL-018 tablets taken orally 20 mg (2 tablets) twice daily
TLL-018 tablets taken orally 30 mg (3 tablets) twice daily
Experimental: Arm C
TLL-018 30 mg. Dose selection for continuation into Stage 2 (Phase III) will be based on efficacy and safety data generated from Stage 1 (Phase II). This dose group may or may not be carried forward into Stage 2.
TLL-018 tablets taken orally 10 mg (1 tablet) twice daily
TLL-018 tablets taken orally 20 mg (2 tablets) twice daily
TLL-018 tablets taken orally 30 mg (3 tablets) twice daily
Placebo-Komparator: Arm D
Placebo. This arm will be used in both Stage 1 (Phase II) and Stage 2 (Phase III).
Placebo taken orally twice daily

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Proportion of trial participants achieving at least 75% improvement from baseline in Eczema Area and Severity Index (EASI-75) at Week 16
Zeitfenster: Week 16
The Eczema Area and Severity Index (EASI) is a validated, physician-assessed tool used to measure the extent and severity of atopic dermatitis (eczema). The total score ranges from 0 to 72, with higher scores indicating more severe disease.
Week 16
Proportion of trial participants achieving an Investigator's Global Assessment (IGA) score of 0 or 1 with a reduction of ≥ 2 points at Week 16
Zeitfenster: Week 16

The Investigator's Global Assessment (IGA) is a physician-reported, static measure used to rate the overall severity of atopic dermatitis at a given time point.

It typically uses a 5-point scale from 0 to 4: 0 = Clear, 4 = Severe.

Week 16

Mitarbeiter und Ermittler

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

Sponsor

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)

31. August 2026

Primärer Abschluss (Geschätzt)

30. September 2029

Studienabschluss (Geschätzt)

30. September 2029

Studienanmeldedaten

Zuerst eingereicht

21. August 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

21. August 2026

Zuerst gepostet (Tatsächlich)

25. August 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

25. August 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

21. August 2026

Zuletzt verifiziert

1. August 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Andere Studien-ID-Nummern

  • TLL-018-305

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

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