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Completed Phase 2 Interventional Accepts healthy volunteers

Dose Ranging Study

ClinicalTrials.gov ID: NCT01802723

Public ClinicalTrials.gov record NCT01802723. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jun 26, 2026, 7:02 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Dose Ranging Study of the Safety and Efficacy of LIPO-202 Healthy Patients With Subcutaneous Fat in the Periumbilical Area

Study identification

NCT ID
NCT01802723
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Neothetics, Inc
Industry
Enrollment
472 participants

Conditions and interventions

Interventions

  • Drug: salmeterol xinafoate Drug
  • Drug: Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 31, 2013
Primary completion
May 31, 2013
Completion
Sep 30, 2013
Last update posted
Mar 25, 2015

2013

United States locations

U.S. sites
22
U.S. states
7
U.S. cities
22
Facility City State ZIP Site status
United States, California Beverly Hills California
United States, California Encinitas California
United States, California Los Angeles California
United States, California San Diego California
United States, California Santa Ana California
United States, Florida Aventura Florida
United States, Florida Clearwater Florida
United States, Florida Lake Worth Florida
United States, Florida Miami Florida
United States, Florida Tampa Florida
United States, Illinois Buffalo Grove Illinois
United States, Illinois Chicago Illinois
United States, New York New York New York
United States, New York Smithtown New York
United States, North Carolina Chapel Hill North Carolina
United States, North Carolina Raleigh North Carolina
United States, Tennessee Nashville Tennessee
United States, Texas Austin Texas
United States, Texas Dallas Texas
United States, Texas Fort Worth Texas
United States, Texas Houston Texas
United States, Texas Plano Texas

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01802723, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 25, 2015 · Synced Jun 26, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01802723 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →