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).
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Notify MeKey information
Conditions
Age range
18 year–80 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 2
Primary location
GSK Investigational Site, Esbjerg, Denmark
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
Primary outcomes
-
Patient safety Tolerability Anti-inflammatory effect (high sensitivity C-reactive Protein)
Time frame: 28 days
Secondary outcomes
-
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.
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