Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT06295172

A Study Comparing Lafullen15 and Lafullen for Temporary Nasolabial Fold Improvement

A Randomized, Evaluator-blind, Matched Pairs, Prospective, Non Inferiority, Confirmatory Study to Compare the Safety and Efficacy Between Lafullen15 and Lafullen in the Correction of Nasolabial Folds

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
73 (estimated)
Sponsor
Samyang Biopharmaceuticals Corporation · Industry
Sex
All
Age
19 Years – 70 Years
Healthy volunteers
Not accepted

Summary

The objective of this clinical trial is to verify the safety and efficacy of Lafullen15 in the temporary improvement of nasolabial Folds

Conditions

Interventions

TypeNameDescription
DEVICELafullen15Apply a maximum of 1.0 ml for each side of the nasolabial fold using both the test device (Lafullen15) and the control device (Lafullen).
DEVICELafullenApply a maximum of 1.0 ml for each side of the nasolabial fold using both the test device (Lafullen15) and the control device (Lafullen).

Timeline

Start date
2024-05-27
Primary completion
2025-09-30
Completion
2026-04-30
First posted
2024-03-06
Last updated
2024-05-14

Source: ClinicalTrials.gov record NCT06295172. Inclusion in this directory is not an endorsement.