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Clinical Trial Summary

This study is being undertaken to:

- evaluate the degree of correction attainable with DL6049 (injectable poly-L-lactic acid)compared to a commercially available CosmoPlastâ„¢ Collagen Implant in the treatment of dermal nasolabial fold wrinkles at 13 months following the last application of study treatment.

- Document the types and incidence of adverse events reported with DL6049 (injectable poly-L-lactic acid)compared with CosmoPlastâ„¢ Collagen Implant. Long term adverse events will be assessed for an additional 12 months following discharge from the main study in subjects treated with DL6049.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00444353
Study type Interventional
Source Bausch Health Americas, Inc.
Contact
Status Completed
Phase Phase 3
Start date August 2004
Completion date January 2007

See also
  Status Clinical Trial Phase
Completed NCT00444210 - DL6049 vs CosmoPlast in the Treatment of Nasolabial Fold Wrinkles Phase 3
Not yet recruiting NCT05162326 - BC-101 in Treatment of Nasolabial Fold Wrinkles Phase 1
Recruiting NCT06013332 - Polymeric Microspheres vs Sculptra® in the Treatment of Moderate to Severe Nasolabial Folds N/A