Status:
ACTIVE_NOT_RECRUITING
Safety and Efficacy in Patients With Moderate to Severe Subacute and Chronic Atopic Dermatitis
Lead Sponsor:
EHL Bio Co., Ltd.
Conditions:
Atopic Dermatitis
Eligibility:
All Genders
19-70 years
Phase:
PHASE2
Brief Summary
A Multicenter, Randomized, Single-Blind, Phase Ⅱ Clinical Trial and Open Label Long-term Observation Study of ADSTEM Inj. to Evaluate the Safety and Efficacy in Patients with Moderate to Severe Subacu...
Detailed Description
This clinical trial is designed with multi-organization, random assignment, single-blind, second-phase clinical trials and open long-term follow up studies, and is intended for patients with secondary...
Eligibility Criteria
Inclusion
- At the time of visit 1, only men and women aged between 19 and 70
- Patients with atopic dermatitis meeting the Hanifin and Rajka diagnostic criteria
- Subacute and chronic patients with symptoms of atopic dermatitis lasting at least 6 months
- Patients with moderate to severe atopic dermatitis who meet all of the following criteria
- SCORAD score ≥ 20points
- EASI score ≥ 12points
- BSA ≥ 10%
- Patients with inadequate response to the stable use of topical atopic dermatitis treatment within 24 weeks prior to study initiation, or those who are unable to administer topical atopic dermatitis treatment due to safety reasons
- Patients who voluntarily agreed in writing to participate in this clinical trial
Exclusion
- Patients with systemic infection symptoms at the time of clinical trials
- Patients with HIV, HBV, HCV, Syphilis test positive
- Patients with uncontrolled asthma disease at the time of clinical trial participation
- Patients who were considered inevitable to receive the medication from 1 month prior to administration of the clinical trial drug to visit 6 such as Immune function modifier(tacrolimus, pimecrolimus, cyclosporine, etc.), and high-frequency topical steroids in Groups 1 to 5, systemic steroids, systemic photochemotherapy, medication that are thought to affect other immune functions (such as immunoglobulin therapy like dupilumab, tralloquinap and desensitization therapy, etc.)
- Women who are pregnant, breastfeeding or have a pregnancy plan up to visit 6 or who do not use available contraceptive methods (women of childbearing age must be negative in screening pregnancy test)
- If patients are the male subject, Those who do not agree to have a contraception during the clinical trial (If the male subject or female partner is infertile, the above-mentioned contravention method is unnecessary)
- Patients participating in other clinical trials or participating in other clinical trials within the last 30 days
- Patients who have experienced significant adverse events during treatment with stem cell therapies
- Patients with stem cell therapy doses or history of participating in clinical trials
- Patients with a history of hypersensitivity to antibiotics and antifungal agents used in the manufacture of medicines for clinical trials
- Patients with renal dysfunction whose creatinine level is more than twice the normal upper limit in the screening test
- Patients with hepatic dysfunction whose AST (Aspartate Amino Transaminase) and ALT (Alanine Amino Transaminase) levels are more than three times the normal upper limit
- Patients who are not suitable for this clinical trial under the judgment of the other examiners
Key Trial Info
Start Date :
December 11 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 31 2027
Estimated Enrollment :
118 Patients enrolled
Trial Details
Trial ID
NCT04137562
Start Date
December 11 2019
End Date
October 31 2027
Last Update
March 15 2024
Active Locations (6)
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1
Chungnam National University Hospital
Daejeon, Chungcheongnam-do, South Korea
2
Korea University AnSan Hospital
Ansan, Gyeonggi-do, South Korea
3
Chung-Ang University Hospital
Seoul, Seoulteukbyeolsi, South Korea
4
Kyunghee University Medical Center
Seoul, Seoulteukbyeolsi, South Korea