ClinicalTrials.gg
Active, not recruitingNCT07582237Updated May 12, 2026

Long-Term Follow-up Study of FURESTEM-AD in Patients With Atopic Dermatitis(K0106)

An observational study in Dermatitis, Atopic, sponsored by Kang Stem Biotech Co., Ltd.. Active, not recruiting at 1 site in South Korea. Open to participants aged 19 Years and older. Per ClinicalTrials.gov, last updated 2026-05-12.

Sponsored by Kang Stem Biotech Co., Ltd. · Observational

Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
262
Ages
19 Years and older
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 82 studies in Dermatitis, Atopic with a site in Korea, Republic of — 6 open to participants now, 17 under way, 6 of them phase 3. Dermatitis, Atopic · Korea, Republic of.

Enrollment
4th of 12
262 · median 101
Started
2021
with 4 others
Observational
12 of 82
3 open now
Primary completion
2028-08
later than 10 of 16 live
Registered
82nd of 82
by date
Lead sponsor
9 of 82
Kang Stem Biotech Co., Ltd.

Among the 82 studies in Dermatitis, Atopic with a site in Korea, Republic of, this one is the 4th largest by enrollment of the 12 observational ones that give a count, is one of 5 that started in 2021, is one of 12 observational ones, reaches primary completion later than 10 of the 16 other live ones, and was the 82nd registered.

Dermatitis, Atopic

1,591 studies on the registry are indexed under Dermatitis, Atopic; 286 are open to participants now.

Browse Dermatitis, Atopic studies →

Open to participants now

6 of the 82 studies in Dermatitis, Atopic with a site in Korea, Republic of are open now. Recruiting first, the newest first:

1 more — sign in →

All 6 open studies →

A study can be open while its sites in Korea, Republic of have not opened yet or have stopped. Only those recruiting at a site in Korea, Republic of →

Who these studies take

Of the 193 Dermatitis, Atopic studies recruiting now, 83 (43%) set no upper age limit and 94 (49%) stop at 75 or younger; 93 take children under 18; 51 take healthy volunteers.

This study: 19 Years and older · all sexes · no healthy volunteers.

The full table on the hub →

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Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 82 studies in Dermatitis, Atopic with a site in Korea, Republic of, or all of them as a file.
02

Study summary

Long-Term Follow-up Study of Subjects With Moderate to Severe Chronic Atopic Dermatitis Who Had Administered FURESTEM-AD Inj. in K0106 Study

03

Conditions studied

  • Dermatitis, Atopic

Browse trials for

Keywords

  • Atopic Dermatitis
  • AD
  • Stem Cell
  • Furestem
04

Who can participate

Ages eligible
19 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Those who participated in the K0106 clinical trial, received FURESTEM-AD Inj., and consented to participate in the long-term follow-up study

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Those who participated in the K0106 clinical trial and received FURESTEM-AD Inj
  • Those who understand and voluntarily sign an form

Exclusion criteria

Exclusion Criteria:

  • None
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
262 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Safety Assessment

    Rate and Number of AESI(Adverse Event of Special Interest) and SS(Special Situation)

    Time frame: 5 years follow-up after treatment

Secondary outcomes

  1. EASI(Eczema Area and Severity Index) Score

    Time frame: 1 year, 2 years, 3 years after treatment

  2. IGA(Investigator's Global Assessment) Score

    Time frame: 1 year, 2 years, 3 years after treatment

  3. Pruritus NRS(Numerical Rating Scale) Score

    Time frame: 1 year, 2 years, 3 years after treatment

07

Study locations

1 site
  • Bucheon Hospital, Soonchunhyang University
    Bucheon-si, South Korea
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Oct 2021 (actual). Primary completion is estimated for Aug 2028, 82 months after the start.

Of 74 industry-sponsored observational studies under Dermatitis, Atopic, half reached primary completion within 32 months of starting (the median), counting those still running; a quarter within 11 and three quarters within 84. This study's planned 82 months is above that.

Counting every sponsor, half of 170 studies reached it within 35 months; a quarter within 17.

How these figures are worked out, and which studies are left out of them.

Registered
May 6, 2026
First posted
May 12, 2026
StartActual
Oct 5, 2021
Primary completionEst.
Aug 21, 2028
CompletionEst.
Feb 21, 2029
Last update
May 12, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on May 12, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07582237
Lead sponsor
Kang Stem Biotech Co., Ltd.
Responsible party
Sponsor
First posted
May 12, 2026
Start date
Oct 5, 2021
Primary completion
Aug 21, 2028 (estimated)
Completion
Feb 21, 2029 (estimated)
Last update
May 12, 2026

Study contacts

Yeonglib Park, professor (CI)
principal investigator · Bucheon Hospital, Soonchunhyang University
Yangwon Lee, professor
principal investigator · Konkuk University Hospital
Sanguk Son, professor
principal investigator · Korea University Ansan Hospital
Bakrin Yoo, professor
principal investigator · Gangdong Kyunghee University Hospital
Jihyun Lee, professor
principal investigator · Seoul St. Mary's Hospital
Donghoon Lee, professor
principal investigator · Seoul National University Hospital
Chanho Na, professor
principal investigator · Chosun University Hospital
Yooin Bae, professor
principal investigator · Hallym University Dongtan Seongsim Hospital
Hyunchang Ko, professor
principal investigator · Yangsan Pusan National University Hospital
Younghyun Jang, professor
principal investigator · Kyungpook National University Hospital
Hoon Kang, professor
principal investigator · The Catholic University of Korea Eunpyeong St. Mary's Hospital
Minkyung Shin, professor
principal investigator · Kyunghee University Hospital
Sanghyun Cho, professor
principal investigator · Catholic University Incheon St. Mary's Hospital
Cheonuk Park, professor
principal investigator · Hallym University Kangnam Sacred Heart Hospital
Jooyeon Ko, professor
principal investigator · Hanyang University
Taeyoung Han, professor
principal investigator · Nowon Eulji University Hospital
Jiyoung Ahn, professor
principal investigator · National medical center
Yuchan Kim, professor
principal investigator · Ajou University School of Medicine
Sungyeol Lee, professor
principal investigator · Soon Chun Hyang University
Junhong Min, professor
principal investigator · KangWon National University Hospital

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in May 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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