Condition: Crow's Feet · Sponsor: S.Biomedics Co., Ltd.
This study is a phase 1/2 clinical trial to evaluate the safety and efficacy of administering clusters of autologous dermal fibroblasts to subjects with periorbital wrinkles on both sides. If subjects who have signed the Informed consent form voluntarily are enrolled in this study, they will be tested for eligibility during the screening period. Subjects will visit the study site a total of 6 times while participating in this study. The subjects who meet the inclusion/exclusion criteria will receive a total of one dose of the IP (Visit 3). Then, the efficacy evaluation will be conducted at Visit 4 (Week 2), Visit 5 (Week 12), and Visit 6 (Week 24), and safety will also be evaluated at each visit.
This description comes directly from the study's public registry record.
Sarang Kim, Master's · 8207022050023 · info@sbiomedics.com
Jong-Wan Kim, Master's · 8207022050023 · jwkim@sbiomedics.com
Always discuss trial participation with your own doctor first.
| Chung-Ang University Hospital | Seoul, South Korea | Recruiting |
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Source record: clinicaltrials.gov/study/NCT04818203