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Clinical Trial Summary

This study will evaluate the long-term safety and duration of efficacy of CCH in the treatment of women with cellulite. This study will be a single day evaluation, approximately 48 months after the first dose of study drug was received in the EN3835-201.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Edema
  • Edematous Fibrosclerotic Panniculopathy

NCT number NCT04381117
Study type Observational
Source Endo Pharmaceuticals
Contact
Status Completed
Phase
Start date May 6, 2020
Completion date June 22, 2020

See also
  Status Clinical Trial Phase
Completed NCT03675685 - Safety and Pharmacokinetics of a Single Dose of CCH (3.36 mg) in Subjects With EFP Phase 1
Completed NCT02942160 - EN3835 for the Treatment of Edematous Fibrosclerotic Panniculopathy (Commonly Known as Cellulite) Phase 2
Completed NCT04580303 - CCH Treatment of Cellulite in the Presence of Dermal Laxity With Comparison Between Two (2) Different Injection Techniques Phase 2
Completed NCT03329989 - Safety and Effectiveness of EN3835 in the Treatment of EFP in Women Phase 2
Completed NCT03893890 - Durability and Safety of EN3835 in the Treatment of EFP (Cellulite) in Women
Completed NCT05419505 - Study of Different Interventions to Reduce Bruising Following CCH-Aaes Treatment for Cellulite of the Buttocks Phase 2
Completed NCT05249257 - Durability and Safety of CCH With Two Different Injection Techniques in Cellulite With Laxity
Completed NCT01518907 - The Safety, Effectiveness, and Pharmacokinetics of AA4500 for the Treatment of Edematous Fibrosclerotic Panniculopathy (Commonly Known as Cellulite) Phase 1
Completed NCT02724644 - EN3835 for the Treatment of Edematous Fibrosclerotic Panniculopathy (Commonly Known as Cellulite) Phase 2
Completed NCT03526549 - Long-Term Study of EN3835 (CCH-aaes) in Edematous Fibrosclerotic Panniculopathy (Cellulite) Phase 3