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Long-term Follow-up Study to Evaluate the Safety and Explore the Efficacy of Multiple Doses of FURESTEM-AD Inj

K

Kangstem Biotech

Status

Not yet enrolling

Conditions

Atopic Dermatitis

Treatments

Other: Not applicable(observational study)

Study type

Observational

Funder types

Industry

Identifiers

NCT04730024
K0104-E

Details and patient eligibility

About

A multi-center, open, long-term follow-up study to Evaluate the Safety and Explore the Efficacy of Multiple Doses of FURESTEM-AD inj. for Moderate to Severe Chronic Atopic Dermatitis: 5-year Results from the K0104 Extension Study

Enrollment

102 estimated patients

Sex

All

Ages

19+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Subject who enrolled K0104 Clinical Trial(parent study).
  2. Subjects who understand and voluntarily sign an informed consent form

Exclusion criteria

  1. Subjects who are expected to be unable to perform at least one follow-up during this study (K0104-E)
  2. Subjects who has received/administered clinical trial drugs or medical devices by participating in other clinical trials until the first visit of this trial (K0104-E) after the completion of K0104 clinical trial
  3. Subjects who are judged to be unsuitable for other researchers to participate in the research

Trial contacts and locations

1

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Central trial contact

Eundoek Yeo; Seulbi Lee

Data sourced from clinicaltrials.gov

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