Long-Term Follow-up Study of FURESTEM-AD in Patients With Atopic Dermatitis(K0106)
Long-Term Follow-up Study of Subjects With Moderate to Severe Chronic Atopic Dermatitis Who Had Administered FURESTEM-AD Inj. in K0106 Study
1 other identifier
observational
262
1 country
1
Brief Summary
Long-Term Follow-up Study of Subjects With Moderate to Severe Chronic Atopic Dermatitis Who Had Administered FURESTEM-AD Inj. in K0106 Study
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Oct 2021
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 5, 2021
CompletedFirst Submitted
Initial submission to the registry
May 6, 2026
CompletedFirst Posted
Study publicly available on registry
May 12, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 21, 2028
ExpectedStudy Completion
Last participant's last visit for all outcomes
February 21, 2029
May 12, 2026
May 1, 2026
6.9 years
May 6, 2026
May 6, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Safety Assessment
Rate and Number of AESI(Adverse Event of Special Interest) and SS(Special Situation)
5 years follow-up after treatment
Secondary Outcomes (3)
EASI(Eczema Area and Severity Index) Score
1 year, 2 years, 3 years after treatment
IGA(Investigator's Global Assessment) Score
1 year, 2 years, 3 years after treatment
Pruritus NRS(Numerical Rating Scale) Score
1 year, 2 years, 3 years after treatment
Eligibility Criteria
Those who participated in the K0106 clinical trial, received FURESTEM-AD Inj., and consented to participate in the long-term follow-up study
You may qualify if:
- Those who participated in the K0106 clinical trial and received FURESTEM-AD Inj
- Those who understand and voluntarily sign an informed consent form
You may not qualify if:
- None
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Bucheon Hospital, Soonchunhyang University
Bucheon-si, South Korea
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Yeonglib Park, professor (CI)
Bucheon Hospital, Soonchunhyang University
- PRINCIPAL INVESTIGATOR
Yangwon Lee, professor
Konkuk University Hospital
- PRINCIPAL INVESTIGATOR
Sanguk Son, professor
Korea University Ansan Hospital
- PRINCIPAL INVESTIGATOR
Bakrin Yoo, professor
Gangdong Kyunghee University Hospital
- PRINCIPAL INVESTIGATOR
Jihyun Lee, professor
Seoul St. Mary's Hospital
- PRINCIPAL INVESTIGATOR
Donghoon Lee, professor
Seoul National University Hospital
- PRINCIPAL INVESTIGATOR
Chanho Na, professor
Chosun University Hospital
- PRINCIPAL INVESTIGATOR
Yooin Bae, professor
Hallym University Dongtan Seongsim Hospital
- PRINCIPAL INVESTIGATOR
Hyunchang Ko, professor
Yangsan Pusan National University Hospital
- PRINCIPAL INVESTIGATOR
Younghyun Jang, professor
Kyungpook National University Hospital
- PRINCIPAL INVESTIGATOR
Hoon Kang, professor
The Catholic University of Korea Eunpyeong St. Mary's Hospital
- PRINCIPAL INVESTIGATOR
Minkyung Shin, professor
Kyunghee University Hospital
- PRINCIPAL INVESTIGATOR
Sanghyun Cho, professor
Catholic University Incheon St. Mary's Hospital
- PRINCIPAL INVESTIGATOR
Cheonuk Park, professor
Hallym University Kangnam Sacred Heart Hospital
- PRINCIPAL INVESTIGATOR
Jooyeon Ko, professor
Hanyang University
- PRINCIPAL INVESTIGATOR
Taeyoung Han, professor
Nowon Eulji University Hospital
- PRINCIPAL INVESTIGATOR
Jiyoung Ahn, professor
National medical center
- PRINCIPAL INVESTIGATOR
Yuchan Kim, professor
Ajou University School of Medicine
- PRINCIPAL INVESTIGATOR
Sungyeol Lee, professor
Soon Chun Hyang University
- PRINCIPAL INVESTIGATOR
Junhong Min, professor
KangWon National University Hospital
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 6, 2026
First Posted
May 12, 2026
Study Start
October 5, 2021
Primary Completion (Estimated)
August 21, 2028
Study Completion (Estimated)
February 21, 2029
Last Updated
May 12, 2026
Record last verified: 2026-05