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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 4 September 2023
Main ID:  NCT03183661
Date of registration: 08/06/2017
Prospective Registration: No
Primary sponsor: Anterogen Co., Ltd.
Public title: A Follow-up Study to Evaluate the Safety of ALLO-ASC-CD in ALLO-ASC-CD-101 Clinical Trial
Scientific title: Follow-up Study to Evaluate the Safety of ALLO-ASC-CD in the Subjects With Crohn´s Disease(ALLO-ASC-CD-101)
Date of first enrolment: November 16, 2016
Target sample size: 9
Recruitment status: Recruiting
URL:  https://clinicaltrials.gov/ct2/show/NCT03183661
Study type:  Observational
Study design:   
Phase: 
Countries of recruitment
Korea, Republic of
Contacts
Name:     Joosung Kim, MD, Ph.D.
Address: 
Telephone:
Email: jooskim@snu.ac.kr,
Affiliation: 
Name:     Young Ho Kim, Ph D
Address: 
Telephone:
Email:
Affiliation:  Samsung Medical Center
Name:     Jae Hee Cheon, Ph D
Address: 
Telephone:
Email:
Affiliation:  Yonsei University
Name:     Jae Hee Cheon, Ph D
Address: 
Telephone:
Email: GENIUSHEE@yuhs.ac
Affiliation: 
Name:     Joo Sung Kim, Ph D
Address: 
Telephone:
Email:
Affiliation:  Seoul National University Hospital
Key inclusion & exclusion criteria

Inclusion Criteria:

1. Subjects who are injected with ALLO-ASC-CD in phase 1 clinical trial of
ALLO-ASC-CD-101.

2. Subjects who are able to give written informed consent prior to study start and to
comply with the study requirements.

Exclusion Criteria:

1. Subjects who are considered not suitable for the study by the principal investigator.



Age minimum: 18 Years
Age maximum: 65 Years
Gender: All
Health Condition(s) or Problem(s) studied
Crohn Disease
Intervention(s)
Biological: ALLO-ASC-CD
Primary Outcome(s)
Number of Participants with Adverse Events as a Measure of Safety and Tolerability [Time Frame: up to 36 months]
Secondary Outcome(s)
Secondary ID(s)
ALLO-ASC-CD-102
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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