An Open-Label Study to Evaluate Retreatment With LIPO-202

Status unconfirmed · Phase 2

Conditions studied: Central Abdominal Bulging

In brief

Evaluate the safety of three 8-week courses of treatment with LIPO-202 in non-obese patients who have central abdominal bulging. Efficacy measurements will also be collected.

Key facts

Study ID

NCT02397525

Run by

Neothetics, Inc

People needed

150

Starts

2015-03-01

Last updated by the study team

2015-08-13

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Provided consent
• Healthy male or non-pregnant female subjects
• BMI < 30 kg/m2
• Stable diet and exercise routine
• Central abdominal bulging that is at least "Slight Bulge, Not Flat"

You may not qualify if…

• Have had any treatment of the fat around your abdomen, including surgical procedures (tummy tuck, liposuction), injections for fat loss or treatments with devices to reduce fat in your abdomen
• Plan on starting a weight loss or exercise program during the study.
• Be a woman who is pregnant, breast feeding, have had a baby within 6 months and/or not using appropriate birth control.
• Known hypersensitivity to study drugs
• Prior or current enrollment in any Neothetics (formerly Lithera) study involving LIPO-102 or LIPO-202

Where it is running

• AboutSkin Dermatology — Englewood, Colorado, United States
• Dermatology Research Institute, LLC — Coral Gables, Florida, United States
• Gwinnett Clinical Research Center, Inc — Snellville, Georgia, United States
• Lupo Center for Aesthetic and General Dermatology — New Orleans, Louisiana, United States
• Bass Plastic Surgery PLLC — New York, New York, United States
• DermResearch Center of New York — Stony Brook, New York, United States
• Dermatology Clinical Research Center of San Antonio — San Antonio, Texas, United States
• Charlottesville Medical Research — Charlottesville, Virginia, United States

Full record on ClinicalTrials.gov

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