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A Study of JYP0066 Cream in Mild-to-Moderate Atopic Dermatitis

2026년 9월 27일 업데이트: Guangzhou JOYO Pharma Co., Ltd

A Multicenter, Randomized, Double-Blind, Placebo-Controlled Phase II Clinical Study to Evaluate the Efficacy and Safety of JYP0066 Topical Cream in Adolescents and Adults With Mild-to-Moderate Atopic Dermatitis

This is a Phase 2 research study testing an investigational topical cream called JYP0066 for the treatment of mild-to-moderate atopic dermatitis (eczema) in teenagers (12-17 years old) and adults. The study will check whether JYP0066 cream can reduce eczema signs and symptoms such as redness, itching, dryness, and skin thickening, and whether it is safe and well tolerated.

Participants will be randomly assigned to one of four groups: they will apply either 4%, 3%, or 2% JYP0066 cream, or a matching placebo cream, to eczema-affected skin twice a day for 8 weeks. All creams will look the same. This helps the study compare which concentration works best and how safe each one is.

연구 개요

상태

아직 모집하지 않음

정황

개입 / 치료

연구 유형

중재적

등록 (추정된)

160

단계

  • 2 단계

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

12년 (어린이, 성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

설명

Inclusion Criteria:

  • Participant is ≥12 and ≤75 years of age at the time of signing informed consent; male or female.

Note: Participants who are ≥12 and <18 years of age at screening and baseline will be classified as adolescents throughout the study.

Body weight ≥40 kg. Meets Williams diagnostic criteria for atopic dermatitis (AD) at screening and baseline, with AD onset at least 6 months before screening.

Williams criteria - Major criterion: itchy skin. Minor criteria: (a) history of flexural dermatitis (elbow/antecubital, popliteal, anterior ankle, neck; in children <10 y, cheek rash); (b) history of asthma or allergic rhinitis (or atopic disease in first-degree relatives for children <4 y); (c) generalized dry skin in recent years; (d) flexural eczema (in children <4 y: cheek/forehead/extensor eczema); (e) onset before age 2 (for patients ≥4 y). Diagnosis = major criterion + ≥3 minor criteria.

vIGA-AD score of 2 (mild) or 3 (moderate) at both screening and baseline. Total AD lesion area of 3%-20% body surface area (BSA) at screening and baseline.

Note: Lesions on scalp, face, and genital area are excluded from BSA calculation at screening and baseline.

Females of childbearing potential must have a negative serum pregnancy test at screening. All participants of childbearing potential (and their partners) must agree to use highly effective contraception from informed consent through 1 month after last study drug administration and must not donate sperm/ova during this period.

Note: Applies also to post-menarchal female adolescents and post-semenarche male adolescents.

Adults: able to understand the purpose and procedures of the study, voluntarily provide written informed consent, and comply with visits/requirements. Adolescents: participant and parent/legal guardian (as applicable) voluntarily provide written informed consent/assent and can communicate with investigator and attend scheduled visits.

Exclusion Criteria:

  • Presence of other skin diseases or skin infections that may interfere with AD assessment at screening/baseline, or large tattoos, birthmarks, or scars over AD lesions at screening/baseline.

Unstable AD, or continuously requiring potent topical corticosteroids to control signs/symptoms.

AD lesions located only or mainly on hands, feet, scalp, face, or genitals with no history of classic flexural involvement.

Known/suspected allergy to any component of study cream or its vehicle, or moderate-to-severe allergic disease at IC signing (e.g., food/drug/detergent allergy; AD-related allergy allowed); or history of moderate-to-severe allergic disease.

Use of any of the following prior to study drug:

Any systemic or topical JAK inhibitor before study entry; Biologics affecting AD (e.g., anti-IL-4, IL-5, IL-12/23, IL-13, IL-31, CD20, TNF-α, IgE) within 12 weeks or 5 half-lives (whichever longer) before study drug; Systemic immunosuppressants/immunomodulators (cyclosporine, MTX, azathioprine, MMF), oral/systemic corticosteroids, PDE4 inhibitors within 4 weeks or 5 half-lives (whichever longer); Systemic herbal/Chinese medicine for AD or other autoimmune-inflammatory diseases within 4 weeks; Phototherapy (NBUVB, UVB, UVA1, PUVA), tanning bed, or other light-emitting device within 4 weeks; Any topical AD treatment (except non-medicated emollient) or antihistamines within 1 week (stable-dose antihistamine before screening allowed); Participation in another clinical trial within 4 weeks or 5 half-lives of investigational product (whichever longer); Any vaccination within 4 weeks, BCG within 1 year, or planned live/attenuated vaccine during study; Long-acting anticoagulants (warfarin, dabigatran) within 4 weeks or need for continuous anticoagulation (aspirin ≤100 mg/day allowed); Strong CYP3A4 inhibitors/inducers (rifampin, fluconazole, itraconazole, ketoconazole, posaconazole, voriconazole, nefazodone) within 2 weeks or 5 half-lives; Allergen-specific immunotherapy within 6 months. Major surgical procedure within 12 weeks before screening. Serious infectious disease within 6 months; history of zoster or disseminated zoster; any infection requiring antibiotics within 2 weeks before screening; or active acute/chronic/local infection at screening; or infection judged by investigator likely to worsen with participation.

Active tuberculosis, untreated latent TB, or incompletely cured TB (by history, symptoms, labs, IGRA, imaging).

Conditions negatively affecting immune response (e.g., organ transplant), or known immunodeficiency (acquired, genetic, or drug-induced).

NYHA Class III/IV heart failure; unstable angina; stroke/TIA; MI; CABG/PCI history; uncontrolled hypertension (SBP >160 or DBP >100 mmHg); hypotension (SBP <90 or DBP <60); clinically significant electrolyte disorder; or other unstable disease affecting safety.

History of thromboembolic event (DVT, pulmonary embolism, CVA) or known genetic hypercoagulable state.

Clinically relevant severe pulmonary disease (e.g., pulmonary hypertension, acute COPD exacerbation, pneumothorax).

Severe GI disease (peptic ulcer, obstruction) or condition affecting drug absorption (e.g., gastrectomy).

Severe hematologic disease (moderate/severe anemia, proliferative bone marrow disease, thrombocytopenia, hemoglobinopathy), severe coagulation abnormality, or high thrombotic risk.

Malignant tumor or lymphoproliferative disease within past 10 years, except adequately treated non-melanoma skin cancer or cervical intraepithelial neoplasia.

Screening 12-lead ECG with prolonged QTcF (>450 ms male, >470 ms female), family history of long QT, or chronic use of QT-prolonging drugs.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 삼루타

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: 4% JYP0066 topical cream - applied twice daily (BID) to affected skin areas for 8 weeks

applied twice daily (BID) to affected skin areas for 8 weeks

실험적: 3% JYP0066 topical cream - applied twice daily (BID) for 8 weeks

applied twice daily (BID) for 8 weeks

실험적: 2% JYP0066 topical cream - applied twice daily (BID) for 8 weeks

applied twice daily (BID) for 8 weeks

위약 비교기: Matching placebo cream (vehicle, no active ingredient) - applied twice daily (BID) for 8 weeks

applied twice daily (BID) for 8 weeks

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
기간
Percent change from baseline in EASI score at Week 8
기간: Baseline to Week 8
Baseline to Week 8

2차 결과 측정

결과 측정
기간
Proportion of participants achieving EASI 50/75/90 at Weeks 1, 2, 4, and 8
기간: Weeks 1, 2, 4, 8
Weeks 1, 2, 4, 8
Percent change from baseline in EASI score at Weeks 1, 2, and 4
기간: Weeks 1, 2, 4
Weeks 1, 2, 4
Proportion of participants with vIGA-AD response at Weeks 1, 2, 4, 8
기간: Weeks 1, 2, 4, 8
Weeks 1, 2, 4, 8
Proportion of participants with vIGA-AD score 0/1 at Weeks 1, 2, 4, 8
기간: Weeks 1, 2, 4, 8
Weeks 1, 2, 4, 8
Proportion of participants with ≥2-point improvement in vIGA-AD from baseline at Weeks 1, 2, 4, 8
기간: Weeks 1, 2, 4, 8
Weeks 1, 2, 4, 8

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 9월 30일

기본 완료 (추정된)

2027년 8월 30일

연구 완료 (추정된)

2027년 12월 31일

연구 등록 날짜

최초 제출

2026년 9월 20일

QC 기준을 충족하는 최초 제출

2026년 9월 20일

처음 게시됨 (실제)

2026년 9월 28일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 9월 30일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 9월 27일

마지막으로 확인됨

2026년 9월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

  • JYP0066M201

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

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