Autologous Human Fibroblasts (azficel-T)
Biological- Collection of 3 mm post auricular skin punch biopsies.
- Three treatment visits with injections administered 5 ± 1 weeks apart on each side of the face.
Other names: LAVIV
NCT Number: NCT00655356
The purpose of this study is to evaluate the safety profile and the treatment effect of Isolagen TherapyTM compared with placebo when administered to bilateral nasolabial fold wrinkles.
Looking for future studies?
Notify Me18 year and older
All sexes
Interventional
Phase 3
Brighton Medical Corporation, Beverly Hills, California, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Other names: LAVIV
Time frame: Baseline (prior to first treatment) and 6 months post final treatment
A two point improvement on the Subject's live assessment of the wrinkles of the lower part of the face as compared to baseline on the Subject Wrinkle Assessment was considered a responder. The Subject Wrinkle Assessment scale was a five point scale with a score of -2 (Very Dissatisfied) being the worst and a score of +2 (Very Satisfied) being the best.
Time frame: Baseline (prior to first treatment) and 6 months after last treatment
A responder was defined as a two point improvement on the blinded Evaluator's live assessment of each of the bilateral nasolabial fold wrinkles at rest using the 6-point ordinal Lemperle Wrinkle Severity Scale. On the Lemperle scale, a score of 5 (Very Deep Wrinkle) is worst and a score of 0 (No Visible Wrinkle) is best.
Time frame: Baseline (prior to first treatment) compared to 3rd treatment visit, 2 and 4 months post final treatment
A two point improvement on the Subject's live assessment of the wrinkles of the lower part of the face as compared to baseline on the Subject Wrinkle Assessment was considered a responder. The Subject Wrinkle Assessment scale was a five point scale with a score of -2 (Very Dissatisfied) being the worst and a score of +2 (Very Satisfied) being the best.
Time frame: Baseline (prior to first treatment) compared to 3rd treatment visit, 2 and 4 months post final treatment
A responder was defined as a two point improvement on the blinded Evaluator's live assessment of each of the bilateral nasolabial fold wrinkles at rest using the 6-point ordinal Lemperle Wrinkle Severity Scale. On the Lemperle scale, a score of 5 (Very Deep Wrinkle) is worst and a score of 0 (No Visible Wrinkle) is best.
Castle Creek Biosciences, LLC.
Industry
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT00649428
Bilateral Nasolabial Fold Wrinkles
Birmingham, Alabama, United States
View Trial Details