- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07693244
Exosome Therapy for Male Androgenetic Alopecia
A Randomized, Double-Blind, Placebo-Controlled Clinical Trial Evaluating the Efficacy and Safety of Human Umbilical Cord Mesenchymal Stem Cell-Derived Exosomes for the Treatment of Male Androgenetic Alopecia
The goal of this clinical trial is to learn if local scalp injection of human umbilical cord mesenchymal stem cell-derived exosomes (hUCMSC-Exos) can treat androgenetic alopecia (AGA) in male patients with AGA.
The main question it aims to answer is:
Does hUCMSC-Exos injection improve hair regrowth compared with placebo?
Researchers will compare hUCMSC-Exos injection to placebo injection to see if hUCMSC-Exos leads to superior efficacy in hair follicle regeneration, as measured by changes in hair density, hair thickness, and patient-reported outcomes.
Participants will:
Receive randomized, double-blinded local scalp injections of either hUCMSC-Exos or placebo
Attend scheduled follow-up visits for hair assessment and safety monitoring
Undergo photography, trichoscopy, and complete quality-of-life or psychosocial burden questionnaires as applicable
연구 개요
상태
정황
상세 설명
Androgenetic alopecia (AGA) is a chronic, progressive condition characterized by gradual miniaturization of hair follicles in a patterned distribution, primarily influenced by genetic susceptibility and androgen-mediated signaling pathways. The condition involves disruption of the hair cycle, particularly shortening of the anagen phase and progressive conversion of terminal hair follicles into vellus-like follicles, ultimately resulting in visible hair thinning and reduced hair density. In addition to its dermatological manifestations, AGA is associated with significant psychological burden, including decreased self-confidence and impaired quality of life.
Current pharmacological interventions mainly aim to slow disease progression rather than fully restore follicular function. However, their limited efficacy and dependency on continuous administration highlight the unmet need for regenerative and disease-modifying therapeutic strategies.
Mesenchymal stem cell-derived exosomes (MSC-Exos) represent a novel class of cell-free biologics with regenerative and immunomodulatory properties. These nano-sized extracellular vesicles contain bioactive molecules such as proteins, lipids, and nucleic acids, which mediate intercellular communication and regulate multiple biological processes. Among different MSC sources, human umbilical cord-derived MSCs are considered to possess advantageous biological characteristics, including higher proliferative capacity, lower immunogenicity, and more stable paracrine activity, making their exosomes particularly suitable for clinical translation.
Experimental studies have demonstrated that MSC-Exos may influence hair follicle biology through multiple complementary mechanisms, including modulation of dermal papilla cell activity, regulation of signaling pathways involved in follicular cycling, enhancement of vascular support within the perifollicular environment, and attenuation of local inflammatory responses. These combined effects may contribute to the reactivation of dormant follicles and support the transition of hair follicles into the anagen growth phase.
This clinical investigation is designed to translate these preclinical findings into a controlled human study setting, aiming to systematically evaluate the therapeutic potential of hUCMSC-derived exosomes for hair regeneration. The study will generate evidence regarding both clinical efficacy and safety profile, providing foundational data for future development of exosome-based regenerative therapies in androgenetic alopecia.
연구 유형
등록 (추정된)
단계
- 2 단계
연락처 및 위치
연구 연락처
- 이름: han Zhang
- 전화번호: 18510009269
- 이메일: zhang_han_0112@163.com
연구 장소
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Beijing, 중국
- 모병
- No.28 Fuxing Road
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연락하다:
- han Zhang
- 전화번호: 18510009269
- 이메일: zhang_han_0112@163.com
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참여기준
자격 기준
공부할 수 있는 나이
- 성인
건강한 자원 봉사자를 받아들입니다
설명
Inclusion Criteria
Participants must meet all of the following criteria to be eligible for enrollment:
- Male subjects aged 18 to 55 years;
- Diagnosis of androgenetic alopecia classified as Norwood-Hamilton grade III-V;
- Stable pattern of hair loss for at least 6 months prior to screening;
- Willingness to refrain from using any other hair loss treatments during the study period and for 6 months after completion of treatment.
Exclusion Criteria
Participants meeting any of the following criteria will be excluded:
- Other types of alopecia, including alopecia areata, cicatricial alopecia, or telogen effluvium;
- Use of minoxidil, finasteride, spironolactone, or other hair growth-related medications within 1 year prior to screening;
- Receipt of platelet-rich plasma (PRP), laser cap therapy, or other scalp procedures within 6 months prior to screening;
- History of autoimmune disease, active scalp infection, coagulation disorders, or malignancy;
- Known hypersensitivity to the investigational product or any of its components;
- Inability to comply with study procedures, incomplete clinical data, or conditions that may interfere with efficacy evaluation;
- Participation in another clinical trial within the study period;
- Any condition that, in the opinion of the investigator, makes the participant unsuitable for the study.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 더블
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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위약 비교기: 일반 식염수 주사
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Sterile 0.9% normal saline injection.
Administered via intradermal scalp injection using the same protocol as the experimental group: 0.05 mL per point, 1 cm spacing, approximately 4 mm depth, once every 4 weeks for a total of 3 sessions.
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실험적: hUCMSC-Exosome Injection
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Sterile exosome suspension derived from human umbilical cord mesenchymal stem cells (hUCMSC-Exos).
Administered via intradermal scalp injection at 0.05 mL per point, 1 cm spacing, approximately 4 mm depth.
Treatment repeated once every 4 weeks for a total of 3 sessions.
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Change in Hair Density From Baseline to Week 24
기간: Baseline to Week 24
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Hair density (hairs/cm²) within a predefined target scalp area will be assessed using digital trichoscopy.
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Baseline to Week 24
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Change in Modified Global Photographic Assessment (MGPA) Score From Baseline to Week 24
기간: Baseline to Week 24
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Global scalp photographs will be evaluated by blinded investigators using the Modified Global Photographic Assessment (MGPA) scale to assess overall improvement in hair growth.
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Baseline to Week 24
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Change in Hair Density From Baseline to Week 12
기간: Baseline to Week 12
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Hair density changes within the predefined target area measured by digital trichoscopy.
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Baseline to Week 12
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Change in Modified Global Photographic Assessment (MGPA) Score From Baseline to Week 12
기간: Baseline to Week 12
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Assessment of global hair growth improvement using standardized photography and MGPA scoring.
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Baseline to Week 12
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Change in Dermatology Life Quality Index (DLQI) Score From Baseline to Week 24
기간: Baseline to Week 24
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Evaluation of treatment-related quality of life improvement using the Dermatology Life Quality Index questionnaire.
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Baseline to Week 24
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Change in Mean Hair Shaft Diameter From Baseline to Week 24
기간: Baseline to Week 24
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Mean hair shaft diameter will be measured using digital trichoscopic analysis.
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Baseline to Week 24
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Change in Hair Type Proportions From Baseline to Week 24
기간: Baseline to Week 24
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Percentage changes in vellus hairs, intermediate hairs, and terminal hairs within the target scalp area.
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Baseline to Week 24
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Subject Satisfaction Score at Week 24
기간: Week 24
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Participant-reported satisfaction regarding overall hair growth improvement and treatment outcomes.
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Week 24
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Investigator Satisfaction Assessment at Week 24
기간: Week 24
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Overall investigator-rated assessment of treatment response and cosmetic improvement.
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Week 24
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공동 작업자 및 조사자
스폰서
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
기본 완료 (추정된)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
- PLAGH-2026-AGA-EXO-001
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
IPD 계획 설명
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .
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