Skip to main content
OpenTrials
Completed

NCT Number: NCT00291902

A Pharmacokinetic Study Of SB-681323 In Subjects With Coronary Heart Disease Undergoing Percutaneous Intervention

Study of SB-681323 (a novel p38 MAPkinase inhibitor) in subjects with documented coronary heart disease (CHD) undergoing elective percutaneous coronary intervention (PCI).

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

GSK Investigational Site, Esbjerg, Denmark

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Females must be of non-child-bearing potential.
  • Female subjects must have a negative pregnancy test.
  • Subjects scheduled to undergo elective single vessel PCI to be performed within the 6 weeks of diagnostic coronary angiography.
  • Must be on stable dose of statin for = 6 weeks prior to screening, with statin tolerability and LDL <130 mg/dL (3.4 mmol/L) at Screening visit.
  • Must be capable of providing informed consent.
  • Have an hsCRP concentration of >2 mg/L, but < 10 mg/L at screening.

Exclusion criteria

  • Women who are pregnant or breast feeding.
  • Planned PCI with multi-vessel stenting.
  • Planned PCI with additional revascularization procedures staged at different days during the study period.
  • Planned PCI other than stenting (e.g., atherectomy, PTCA without stenting, etc).
  • Planned PCI of any bypass graft.
  • History of CABG surgery.
  • Planned cardiac or major non-cardiac surgery within the study period.
  • Disabling stroke in the past 6 months.
  • History of chronic viral hepatitis or other chronic hepatic disorders.
  • History of Gilbert's syndrome or elevated bilirubin concentrations at screening.
  • History of increased liver function tests (ALT, AST) due to acute or chronic liver conditions, above the upper limit of normal at screening or in the past 6 months.
  • Renal impairment with serum creatinine >2.0 mg/dl (177umol/L) at Screening, or history of kidney transplant, or a history of contrast nephropathy.
  • Current inadequately controlled hypertension (blood pressure >160 mmHg systolic and/or >100 mmHg diastolic) on a stable dose of antihypertensive medication.
  • Current poorly controlled diabetes mellitus, defined as HbA1c >10% at Screening.
  • History of severe heart failure defined as NYHA class III or IV or those with known severe LV dysfunction (EF<30%) regardless of symptomatic status.
  • History of malignancy within the past 5 years, other than non-melanoma skin cancer.
  • Current life-threatening condition other than vascular disease that may prevent a subject from completing the study.
  • Alcohol or drug abuse within the past 6 months.

Treatment and study plan

SB-681323

Drug

Primary outcomes

  1. Patient safety Tolerability Anti-inflammatory effect (high sensitivity C-reactive Protein)

    Time frame: 28 days

Secondary outcomes

  1. Anti-inflammatory effect (biomarkers) Endothelial function (peripheral artery tonometry) Pharmacokinetics

    Time frame: 28 days

Sponsors and collaborators

Lead sponsor

GlaxoSmithKline

Industry

Registry information

Official study title

A 28-day, Randomized, Double-blind, Placebo-controlled Study to Assess the Safety, Tolerability, Anti-inflammatory Effect and Steady-state Pharmacokinetics of SB-681323 (7.5 mg) in Subjects With Coronary Heart Disease (CHD) Undergoing Elective Percutaneous Coronary Interventions (PCI)

Important dates

Study start
2006
First posted
Feb 15, 2006
Registry last updated
Jun 4, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.