Dermatitis, Atopic Clinical Trial
Official title:
A Long-Term Safety Follow-Up Study of SCM AGH in Subjects Who Participated in the ADT2002 Study
Verified date | March 2021 |
Source | SCM Lifescience Co., LTD. |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
This is a long-term safety follow-up study of the Phase I/II multicenter study of SCM-AGH in subjects with moderate to severe atopic dermatitis. subjects will be followed up for a maximum period of 240 weeks after the first dose of investigational product. Only subjects previously enrolled in protocol ADT2002 (ClinicalTrials.gov ID: NCT04179760) will be eligible for this long-term follow-up protocol.
Status | Enrolling by invitation |
Enrollment | 92 |
Est. completion date | March 31, 2025 |
Est. primary completion date | January 31, 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 19 Years and older |
Eligibility | Inclusion Criteria: 1. Subjects who provide written informed consent 2. Subjects who have received at least 1 dose of SCM-AGH in the ADT2002 study 3. Subjects who are willing to comply with the visit schedule and study requirements for reporting relevant information to the site. Exclusion Criteria: 1. Subjects who are unable to comply with the visit schedule prior to Week 240 after first dose of SCM AGH |
Country | Name | City | State |
---|---|---|---|
Korea, Republic of | Inha University Hospital | Incheon |
Lead Sponsor | Collaborator |
---|---|
SCM Lifescience Co., LTD. |
Korea, Republic of,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Long-term safety assessment of SCM-AGH in subjects with moderate to severe Atopic Dermatitis(AD) | Number of occurrence of treatment-related adverse events (= Grade 3 in severity (NCI-CTCAE, v5.0)) | Up to 5 Years | |
Primary | Long-term concomitant medication assessment of SCM-AGH in subjects with moderate to severe Atopic Dermatitis(AD) | Number of occurrence of use of medications related to adverse events | Up to 5 Years | |
Secondary | Outcome of unresolved Adverse Events(AEs) from ADT2002 study | Up to 5 Years | ||
Secondary | Clinically important physical examination findings | Number of abnormality in general appearance, skin, eyes/ears/nose/throat, head and neck, cardiovascular, respiratory, abdomen, extremities, lymph nodes, musculoskeletal and neurologic. | Up to 5 Years | |
Secondary | Number of occurrence of Abnormal, clinically significant in hematology laboratory results | Hematology panel: alkaline phosphatase [ALP], blood urea nitrogen, creatinine, serum aspartate aminotransferase (AST), serum alanine aminotransferase (ALT), albumin, total protein, total bilirubin, uric acid, glucose, cholesterol, sodium, potassium, chloride, calcium, phosphorus | Up to 5 Years | |
Secondary | Number of occurrence of Abnormal, clinically significant in chemistry laboratory results | Chemistry panel: hemoglobin, hematocrit, red blood cells, white blood cells (WBC), WBC differential count, platelets | Up to 5 Years | |
Secondary | Number of occurrence of Abnormal, clinically significant in urinalysis laboratory results | Urinalysis panel: specific gravity (SG), color, pH, protein, glucose, bilirubin, blood, WBC | Up to 5 Years |
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