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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 Oct 21, 2026, 2:39 AM 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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Dose Ranging Study

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

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
Feb 2013 (Type not available)
Primary completion
Jun 2013 (Actual)
Completion
Oct 2013 (Actual)
Last update posted
Mar 26, 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 26, 2015 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01802723 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →