Safety and Efficacy Study of EXC 001 to Improve the Appearance of Scars From Prior Breast Surgery

Completed · Phase 2 · Has a placebo group

Conditions studied: Scar Prevention

In brief

This study will compare how well EXC 001 works to improve the appearance of scars in subjects undergoing breast scar revision surgery. The study will also evaluate the safety of EXC 001 in healthy adult subjects.

Key facts

Study ID

NCT01037413

Run by

Pfizer

People needed

25

Starts

2009-12-22

Expected to finish

2010-04-09

Last updated by the study team

2021-08-02

Who can join

Age: 18 and older, up to 55. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Subjects must have previously had breast surgery resulting in unacceptable scars
• Subject has chosen to have the breast scars revised
• Subjects must not be pregnant or lactating

You may not qualify if…

• Currently pregnant or pregnant during the 6 months prior to inclusion in the study, or lactating
• Participation in another clinical trial within 30 days prior to the start of the study
• Any other condition or prior therapy, which, in the opinion of the PI, would make the subject unsuitable for this study

Where it is running

• Scripps medical — La Jolla, California, United States
• Northwestern University,Division of Plastic Surgery — Chicago, Illinois, United States
• Body Aesthetic Plastic Surgery — St Louis, Missouri, United States
• Jewell Plastic Surgery Center — Eugene, Oregon, United States
• Connall Consmetic Surgery — Tualatin, Oregon, United States

Full record on ClinicalTrials.gov

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