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Not Yet RecruitingNCT06402058

A Study Comparing DMSB01 and Rejuran® for Temporary Crow's Feet Lines Improvement

A Randomized, Subject and Evaluator Blinded, Matched Pairs, Pilot Study to Evaluate the Safety and Efficacy of DMSB01 According to the Number of Injections in Subjects With Crow's Feet Lines Compared to Control Device

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Samyang Biopharmaceuticals Corporation · Industry
Sex
All
Age
19 Years
Healthy volunteers
Not accepted

Summary

The objective of this Pilot Study is to verify the safety and efficacy of DMSB01 in the temporary improvement of Crow's Feet Lines

Conditions

Interventions

TypeNameDescription
DEVICEDMSB01Apply a maximum of 1.0 ml for each side of the Crow's Feet Lines using both the test device (DMSB01) and the control device (Rejuran®).
DEVICERejuran®Apply a maximum of 1.0 ml for each side of the Crow's Feet Lines using both the test device (DMSB01) and the control device (Rejuran®).

Timeline

Start date
2024-06-10
Primary completion
2025-01-31
Completion
2025-04-30
First posted
2024-05-07
Last updated
2024-05-13

Source: ClinicalTrials.gov record NCT06402058. Inclusion in this directory is not an endorsement.

A Study Comparing DMSB01 and Rejuran® for Temporary Crow's Feet Lines Improvement (NCT06402058) · Clinical Trials Directory