Safety and Efficacy of FURESTEM-AD Inj. in Patients With Moderately Subacute and Chronic Atopic Dermatitis (AD)

Phase I/IIa Clinical Trial to Evaluate the Efficacy and Safety of FURESTEM-AD Inj. in Patients With Moderately Subacute and Chronic Atopic Dermatitis

The purpose of phase I clinical trial is to evaluate safety and efficacy in subjects with over Moderately subacute and chronic Atopic Dermatitis after inject. Also, The purpose of phase IIa clinical trial is to determine clinically proper dose capacity of FURESTEM-AD Inj. by evaluating safety and efficacy based on SCORAD INDEX in subjects with over Moderately subacute and chronic Atopic Dermatitis.

Study Overview

• Status: Completed
• Conditions: Atopic Dermatitis
• Intervention / Treatment: Biological: FURESTEM-AD Inj.

Detailed Description

Atopic dermatitis is recurring and chronic Allergic eczema which accompanies serious itching and xeroderma. Atopic dermatitis has special features such as increase of acidophil, high expression ratio of IgE in the blood. Recently, Atopic dermatitis is estimated to developing for 10 to 20 percent of the population in the world. However, there is no distinguished treatment to completely recover. Especially, most of diagnosis are made when the patients are younger than 5 years old. Moreover, 50 percent of them get diagnose Atopic dermatitis between 6 month and 24 month. According to the National epidemiological investigation conducted by the Korean Academy of Pediatric Allergy and Respiratory Disease, Outbreak ratio of Atopic dermatitis continually increase for the past decade. Accordingly, it has become a major social concern. It is really important for the patients to care and diagnose as soon as they find out symptoms of Atopic dermatitis. The reason is that 50 to 75 percent of the Atopic dermatitis patients are suffering from Allergies which cause asthma and rhinitis. Recently, It has been reported that Mesenchymal stem cells have special abilities to restrict the growth of lymphocyte non-specific and to restrict the activation of lymphocyte by the stimulus of mitogen or antigen. It is also reported that the restrict of lymphocyte by Mesenchymal stem cells does not need HLA-matching unlike the case of T-cell. It has been found that Mesenchymal stem cells' ability of autoimmune induction is weak because of low expression of antigen like HLA-DR. It is also discovered that Mesenchymal stem cells do not cause autoimmune side-effect even though we inject them in the body. When the body get infected by the pathogens, innate immune response operate as the primary defence mechanism. at this time, there are some receptors reacting first such as TLR(toll-like receptor) and NLR(nucleotide-binding oligomerization domain) which is located in the cytoplasm of a cell. It is reported that the activities of TLR which is expressed by Mesenchymal stem cells play an important roles about immunomodulatory ability of Mesenchymal stem cells. Furthermore, human Umbilical Cord Blood derived-Universal Stem Cells( hUCB-USCs) manifest TLR and NLR of Mesenchymal Stem cells at the same time. when those receptors become activation, it maximize ability of immunomodulatory. Therefore, hUCB-USCs can be utilized to cure intractable autoimmune disease like Atopic dermatitis. Further, It has huge possibility as cell therapy products for autoimmune disease.

• Study Type: Interventional
• Enrollment (Actual): 34
• Phase: Phase 2; Phase 1

Contacts and Locations

Study Locations

• Korea, Republic of
  • Seoul, Korea, Republic of, 137-701
    • Catholic Medical Center

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 20 years to 60 years (Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Of either gender, aged ≥20 and ≤60 years
• Atopic Dermatitis subjects who are coincident with Hanifin and Rajka diagnosis criteria
• subacute and chronic Atopic subjects who have Atopic Dermatitis symptoms continually at least 6 months
• Subjects with over moderate atopic dermatitis( SCORAD score > 20 )
• Subjects who understand and voluntarily sign an informed consent form

Exclusion Criteria:

• Subjects who have systemic infection at the baseline visit
• Subjects who have asthma at the baseline visit
• Treatment with oral corticosteroids, oral antibiotics, whole body photochemotherapy, immunosuppressive drug within 4 weeks before the baseline visit
• Treatment with topical steroids, antibiotics within 2 weeks before the baseline visit
• Subjects who already took or need to take the medicine which is prohibited to take during the clinical study.
• Pregnant, breast-feeding women or women who plan to become pregnant during this study. (Females of Childbearing Potential must have a negative urine pregnancy test at Screening and Baseline)
• Subjects who currently participate in other clinical trial or participated in other clinical trial within 30 days
• Creatinine value ≥ 2 Upper limit of the normal range at screening test
• AST/ALT value ≥ 2 Upper limit of the normal range at screening test
• Any other condition which the investigator judges would make patient unsuitable for study participation

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Treatment; FURESTEM-AD Inj. 1. 2.5 x 10^7 stem cells after registration. FURESTEM-AD Inj. 2. 5.0 x 10^7 stem cells after registration.	Biological: FURESTEM-AD Inj.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
over 50% reduction ratio of SCORAD INDEX as contrasted with baseline value	4 weeks follow-up after treatment

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
SCORAD Total Score		4 weeks follow-up after treatment
the degrees of disease		4 weeks follow-up after treatment
Valuation of IGA		4 weeks follow-up after treatment
each index of SCORAD INDEX	TBSA, erythema, edema/papulation, oozing, excoriations, dryness, lichenification, pruritus, insomnia.	4 weeks follow-up after treatment
serum Total IgE		4 weeks follow-up after treatment
Valuation of EASI		4 weeks follow-up after treatment

Collaborators and Investigators

• Sponsor: Kang Stem Biotech Co., Ltd.
• Investigators: Principal Investigator: Taeyoon Kim, Catholic Medical Center

Study record dates

Study Major Dates

• Study Start: September 1, 2013
• Primary Completion (Actual): May 1, 2015
• Study Completion (Actual): May 1, 2015

Study Registration Dates

• First Submitted: August 20, 2013
• First Submitted That Met QC Criteria: August 22, 2013
• First Posted (Estimate): August 23, 2013

Study Record Updates

• Last Update Posted (Estimate): October 6, 2016
• Last Update Submitted That Met QC Criteria: October 5, 2016
• Last Verified: August 1, 2015

More Information

Terms related to this study

• Keywords: Atopic dermatitis; Cell therapy; AD; Stem cell; skin disease; furestem; hUCB-MSC; UCB-MSC; Umbilical cord Blood
• Additional Relevant MeSH Terms: Skin Diseases; Immune System Diseases; Hypersensitivity, Immediate; Genetic Diseases, Inborn; Skin Diseases, Genetic; Hypersensitivity; Skin Diseases, Eczematous; Dermatitis; Eczema; Dermatitis, Atopic
• Other Study ID Numbers: KSB-AD