Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00297180 · ClinicalTrials.gov registry record · Phase 2

Weight Loss In Obese Subjects Taking Either GW869682 Or Placebo 3 Times Per Day For 12 Weeks

A Phase 2 study of Obesity, sponsored by GlaxoSmithKline.

Completed
Registry status
Phase 2
Development phase
136
Enrollment target
3
Study locations

NCT00297180: Completed Phase 2 study of Obesity, sponsored by GlaxoSmithKline.

NCT00297180 is a Phase 2 study of Obesity that has completed, run by GlaxoSmithKline. The registered enrollment target is 136 participants, below the 819-participant average among 1,053 other Obesity trials with a reported enrollment target (83% lower). The trial reports 3 study locations across 3 states. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00297180, a Phase 2 study of Obesity, has completed, sponsored by GlaxoSmithKline.

COMPLETED
Registry status
Phase 2
Development phase
136 participants
Enrollment target
3
Study locations

Study Summary

GW869682 causes glucose to be excreted in the urine. The purpose of this study is to see whether enough calories from glucose are excreted in the urine to cause weight loss.

Conditions Studied

Interventions

  • DRUG GW869682

Study Locations (3)

Florida

  • GSK Investigational Site - Daytona Beach

Louisiana

  • GSK Investigational Site - Baton Rouge

Oregon

  • GSK Investigational Site - Portland

Trial Details

FieldValue
Enrollment Target 136 participants
Start Date 2006-01
Est. Completion 2006-09
Phase Phase 2
GlaxoSmithKline

1,345 total trials

What the finished NCT00297180 record still lists

NCT00297180 is an interventional study that assigns participants to a tested intervention. The registered 136 participants enrollment target is mid-sized for trials with a published cap, below the 819-participant average among 1,053 other Obesity trials with a reported enrollment target (83% lower).

The record links to 1 condition, with Obesity appearing as the primary indexed condition, and to 1 intervention - of which GW869682 is the first listed.

NCT00297180 reports a single indexed study location in Florida, Louisiana, Oregon.

Frequently Asked Questions

What is clinical trial NCT00297180 about?

NCT00297180 is a clinical study titled "Weight Loss In Obese Subjects Taking Either GW869682 Or Placebo 3 Times Per Day For 12 Weeks". GW869682 causes glucose to be excreted in the urine. The purpose of this study is to see whether enough calories from glucose are excreted in the urine to cause weight loss.

What is the current status of trial NCT00297180?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 136 participants. The study started on 2006-01. Estimated completion is 2006-09.

What conditions does trial NCT00297180 study?

This clinical trial studies the following conditions: Obesity.

What interventions are being tested in trial NCT00297180?

The interventions under investigation include: GW869682 (DRUG).

Who is sponsoring clinical trial NCT00297180?

This trial is sponsored by GlaxoSmithKline, which has 1,345 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00297180 being conducted?

This trial has 3 study locations across Florida, Louisiana, Oregon. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Obesity

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00297180's enrollment target sits among peer trials

136 407th of 1053 higher than 641 of 1,053 other Obesity trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Obesity trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01555892 · 136 participants · Phase 1

    Cytotoxic T-Lymphocytes for EBV-positive Lymphoma, GRALE

  • NCT03216525 · 136 participants · Phase 3

    Alvimopan Versus Placebo in Patients Undergoing Radical Cystectomy on an Enhanced Recovery Protocol

  • NCT04476901 · 136 participants · Phase 2

    Administration of Allogeneic-MSC in Patients With Non-Ischemic Dilated Cardiomyopathy

  • NCT04603898 · 136 participants · NA

    Oxalate Formation From Ascorbic Acid

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00297180, the US trial registry maintained by the National Library of Medicine. NCT00297180 (mid enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.