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COMPLETED Phase 2

Study to Evaluate the Safety and Efficacy of LIPO-202 for the Reduction of Submental Subcutaneous Fat

NCT03005717 · View on ClinicalTrials.gov ↗

Study Summary

Study LIPO-202-CL-31 is a multi center, randomized, double-blind, placebo-controlled study to evaluate the safety and efficacy of two different doses of LIPO-202 versus placebo on submental bulging due to subcutaneous fat. Approximately 150 participants of either gender who have a "Moderate Bulge" or "Large Bulge" in the submental fat (on Patient-Reported Submental Bulging Scale \[PR-SBS\] and Clinician-Reported Submental Bulging Scale \[CR-SBS\]) will be recruited for this study.

Conditions Studied

Interventions

  • DRUG LIPO-202
  • DRUG Placebo for LIPO-202

Study Locations (11)

California

  • Clinical Testing of Beverly Hills — Beverly Hills
  • Ablon Skin Institute And Research Center — Manhattan Beach

Colorado

  • AboutSkin Research — Greenwood Village

Florida

  • Skin Research Institute — Coral Gables

Michigan

  • Grekin Skin Institute — Warren

Minnesota

  • Minnesota Clinical Study Center — Fridley

Missouri

  • Mercy Research — Washington

Nebraska

  • Skin Specialists, PC — Omaha

New York

  • Juva Skin & Laser Center — New York

Trial Details

FieldValue
Enrollment Target 162 participants
Start Date 2016-12-22
Est. Completion 2017-06-02
Phase Phase 2

Sponsor

Neothetics

2 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03005717

The ClinicalTrials.gov registry entry for NCT03005717 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 162 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Neothetics, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Submental Fat appearing as the primary indexed condition, and to 2 interventions — of which LIPO-202 is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT03005717 reports 11 study locations spanning 10 distinct geographic areas — top geographies include California, Colorado, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT03005717 about?

NCT03005717 is a clinical study titled "Study to Evaluate the Safety and Efficacy of LIPO-202 for the Reduction of Submental Subcutaneous Fat". Study LIPO-202-CL-31 is a multi center, randomized, double-blind, placebo-controlled study to evaluate the safety and efficacy of two different doses of LIPO-202 versus placebo on submental bulging due to subcutaneous fat. Approximately 150 participants of either gender who have a "Moderate Bulge" o...

What is the current status of trial NCT03005717?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 162 participants. The study started on 2016-12-22. Estimated completion is 2017-06-02.

What conditions does trial NCT03005717 study?

This clinical trial studies the following conditions: Submental Fat. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03005717?

The interventions under investigation include: LIPO-202 (DRUG), Placebo for LIPO-202 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03005717?

This trial is sponsored by Neothetics, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03005717 being conducted?

This trial has 11 study locations across California, Colorado, Florida, Michigan, Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial