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NCT00783549 · ClinicalTrials.gov registry record · Phase 1

A Study in Healthy Volunteers of Single Doses of Orally Administered Investigational Product to Investigate Safety, Tolerability, and Pharmacokinecs.

A Phase 1 study, sponsored by GlaxoSmithKline.

Completed
Registry status
Phase 1
Development phase
76
Enrollment target

NCT00783549: Completed Phase 1 study, sponsored by GlaxoSmithKline.

NCT00783549 is a Phase 1 study that has completed, run by GlaxoSmithKline. The registered enrollment target is 76 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (27% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00783549, a Phase 1 study, has completed, sponsored by GlaxoSmithKline.

COMPLETED
Registry status
Phase 1
Development phase
76 participants
Enrollment target

Study Summary

This study is the first study in humans to assess the safety and tolerability of various doses of GSK1292263 alone, and taken with sitigliptan.

Interventions

  • DRUG an undetermined dose of GSK1292263
  • DRUG ascending dose of GSK1292263

Trial Details

FieldValue
Enrollment Target 76 participants
Start Date 2008-09-04
Est. Completion 2009-03-31
Phase Phase 1
GlaxoSmithKline

1,345 total trials

What the finished NCT00783549 record still lists

NCT00783549 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 76 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (27% higher).

The record links to 0 conditions, and to 2 interventions - of which an undetermined dose of GSK1292263 is the first listed.

NCT00783549 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00783549 about?

NCT00783549 is a clinical study titled "A Study in Healthy Volunteers of Single Doses of Orally Administered Investigational Product to Investigate Safety, Tolerability, and Pharmacokinecs.". This study is the first study in humans to assess the safety and tolerability of various doses of GSK1292263 alone, and taken with sitigliptan.

What is the current status of trial NCT00783549?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 76 participants. The study started on 2008-09-04. Estimated completion is 2009-03-31.

What interventions are being tested in trial NCT00783549?

The interventions under investigation include: an undetermined dose of GSK1292263 (DRUG), ascending dose of GSK1292263 (DRUG).

Who is sponsoring clinical trial NCT00783549?

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

How this trial's enrollment target compares

Where NCT00783549's enrollment target sits among peer trials

76 705th of 2000 higher than 1,290 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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

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Source: ClinicalTrials.gov NCT00783549, the US trial registry maintained by the National Library of Medicine. NCT00783549 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.