The purpose of this clinical trial is to evaluate long-term safety and efficacy in patients who has history of FURESTEM-CD injection at least once.
This study is an extended study of KSTHD\_FURESTEM-CD phase 1 / 2a clinical trials in patients with moderate active Crohn's disease who had received at least once a FURESTEM-CD injection. The purpose of this clinical trial is to evaluate long-term safety and efficacy in patients for approximately 36 months (144 weeks).
Study Type
OBSERVATIONAL
Enrollment
24
IV infusion
Inje University Haeundae Paik Hospital
Busan, South Korea
RECRUITINGYeungnam University Medical Center
Daegu, South Korea
RECRUITINGSeoul National Universtiy Bundang Hospital
Seongnam-si, South Korea
all kinds of adverse events which occur during the clinical sutdy
Safety outcome
Time frame: 114 weeks
ratio of patients who is applicable to CDAI<150
Efficacy outcome
Time frame: 114 weeks
ratio of patients who reduce CDAI over 70 as contrasted witd baseline(V7)
Efficacy outcome
Time frame: 114 weeks
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Severance Hospital
Seoul, South Korea
RECRUITINGAsan Medical Center
Seoul, South Korea
RECRUITINGSoeul National University Hospital
Soeul, South Korea
RECRUITINGThe Catholic University of Korea, St. Vincent'S Hospital.
Suwon, South Korea
RECRUITING