drugset / Trial / NCT06533540

Safety Study of TPX-121 on Nasolabial Folds

NCT06533540 ↗

Phase 1 Active not recruiting 18 enrolled Tego Science, Inc.
Non-randomizedParallel-groupOpen-labelTreatment

Summary

Nasolabial folds augmentation is possible through dermal filler and botulinum toxin, however, safety issues are existed as well as efficacy. Therefore, there is a need for a safer procedure for nasolabial folds correction. This study (Project No. TPX-121) assesses the safety of allogeneic fibroblasts (TPX-115) on nasolabial folds. The safety endpoint is dose-limiting toxicity (DLT). In addition, exploratory endpoints are the improvement of nasolabial folds in Wrinkle Severity Rating Scale (WSRS) at week 4 and 12, change in WSRS and Wrinkle Severity Scale (WSS) at week 4 and 12, and overall appearance improvement rate in Global Aesthetic Improvement Scale (GAIS) at week 4 and 12.

Timeline

Start
2024-12-11
Primary completion
2026-03
Completion
2026-12

Drugs

EvaluationDrugModalityDoseRoute
Subject TPX-115 Cell therapy — Other

Indications