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NCT00551694

A Second Study to Evaluate Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of a Single and a Repeat Oral Dose of GSK256073A in Healthy Adult Subjects

Completed Phase 1 Last updated 31 May 2012
What this trial tests

Phase 1 trial testing GSK256073A tablets in Healthy Subjects in 4 participants. Completed in 1 December 2007.

Timeline
1 October 2007
Primary endpoint
1 December 2007
1 December 2007

Quick facts

Lead sponsorGlaxoSmithKline
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designsingle group
Maskingnone
Primary purposediagnostic
Enrollment4
Start date1 October 2007
Primary completion1 December 2007
Estimated completion1 December 2007
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

GlaxoSmithKline — full company profile →

Who can join

Adults 18 to 55, any sex, with Healthy Subjects or Dyslipidaemias. Healthy volunteers can join.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

The purpose of this study is to compare the effects of single and repeat doses of GSK256073 with placebo in HVT subjects that have been administrated GSK256073 in the HMA107787 study

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. GPCRs involved in metabolic diseases: pharmacotherapeutic development updates.
    Jin C, Chen H, Xie L, Zhou Y, et al · · 2024 · cited 25× · PMID 38326623 · DOI 10.1038/s41401-023-01215-2

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Other recruiting trials for Healthy Subjects

Currently open trials in the same condition.

Other GlaxoSmithKline trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00551694.

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