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Exosome Therapy for Male Androgenetic Alopecia

2026년 7월 6일 업데이트: Zhang Han

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

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

중재적

등록 (추정된)

120

단계

  • 2 단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 장소

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

  • 성인

건강한 자원 봉사자를 받아들입니다

아니

설명

Inclusion Criteria

Participants must meet all of the following criteria to be eligible for enrollment:

  1. Male subjects aged 18 to 55 years;
  2. Diagnosis of androgenetic alopecia classified as Norwood-Hamilton grade III-V;
  3. Stable pattern of hair loss for at least 6 months prior to screening;
  4. 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:

  1. Other types of alopecia, including alopecia areata, cicatricial alopecia, or telogen effluvium;
  2. Use of minoxidil, finasteride, spironolactone, or other hair growth-related medications within 1 year prior to screening;
  3. Receipt of platelet-rich plasma (PRP), laser cap therapy, or other scalp procedures within 6 months prior to screening;
  4. History of autoimmune disease, active scalp infection, coagulation disorders, or malignancy;
  5. Known hypersensitivity to the investigational product or any of its components;
  6. Inability to comply with study procedures, incomplete clinical data, or conditions that may interfere with efficacy evaluation;
  7. Participation in another clinical trial within the study period;
  8. Any condition that, in the opinion of the investigator, makes the participant unsuitable for the study.

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: 더블

무기와 개입

참가자 그룹 / 팔
개입 / 치료
위약 비교기: 일반 식염수 주사
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.
실험적: hUCMSC-Exosome Injection
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.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Change in Hair Density From Baseline to Week 24
기간: Baseline to Week 24
Hair density (hairs/cm²) within a predefined target scalp area will be assessed using digital trichoscopy.
Baseline to Week 24
Change in Modified Global Photographic Assessment (MGPA) Score From Baseline to Week 24
기간: Baseline to Week 24
Global scalp photographs will be evaluated by blinded investigators using the Modified Global Photographic Assessment (MGPA) scale to assess overall improvement in hair growth.
Baseline to Week 24

2차 결과 측정

결과 측정
측정값 설명
기간
Change in Hair Density From Baseline to Week 12
기간: Baseline to Week 12
Hair density changes within the predefined target area measured by digital trichoscopy.
Baseline to Week 12
Change in Modified Global Photographic Assessment (MGPA) Score From Baseline to Week 12
기간: Baseline to Week 12
Assessment of global hair growth improvement using standardized photography and MGPA scoring.
Baseline to Week 12
Change in Dermatology Life Quality Index (DLQI) Score From Baseline to Week 24
기간: Baseline to Week 24
Evaluation of treatment-related quality of life improvement using the Dermatology Life Quality Index questionnaire.
Baseline to Week 24
Change in Mean Hair Shaft Diameter From Baseline to Week 24
기간: Baseline to Week 24
Mean hair shaft diameter will be measured using digital trichoscopic analysis.
Baseline to Week 24
Change in Hair Type Proportions From Baseline to Week 24
기간: Baseline to Week 24
Percentage changes in vellus hairs, intermediate hairs, and terminal hairs within the target scalp area.
Baseline to Week 24
Subject Satisfaction Score at Week 24
기간: Week 24
Participant-reported satisfaction regarding overall hair growth improvement and treatment outcomes.
Week 24
Investigator Satisfaction Assessment at Week 24
기간: Week 24
Overall investigator-rated assessment of treatment response and cosmetic improvement.
Week 24

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 (실제)

2026년 4월 30일

기본 완료 (추정된)

2026년 11월 10일

연구 완료 (추정된)

2026년 11월 10일

연구 등록 날짜

최초 제출

2026년 7월 6일

QC 기준을 충족하는 최초 제출

2026년 7월 6일

처음 게시됨 (실제)

2026년 7월 9일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 7월 9일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 7월 6일

마지막으로 확인됨

2026년 7월 1일

추가 정보

이 연구와 관련된 용어

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

미정

IPD 계획 설명

Individual participant data (IPD) sharing has not yet been determined. Data sharing policies will be considered after study completion in accordance with institutional regulations, ethical requirements, and participant privacy protection.

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

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. .

남성형 탈모증(AGA)에 대한 임상 시험

Human Umbilical Cord Mesenchymal Stem Cell-Derived Exosomes에 대한 임상 시험

3
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