Last updated: 11/04/2018 10:17:09
A study to evaluate the effects of 3 months dosing with GW856553, as assessed FDG-PET/CT imaging
EudraCT ID
EU CT Number
Not applicable
Trial status
Completed
Completed
Trial overview
Official title: A double-blind, placebo-controlled, parallel group study to evaluate the effects of two regimens of GW856553, over a period of 3 month, on in-vivo macrophage activity, as assessed by FDG-PET/CT imaging, in the carotid arteries and aorta of subjects with established atherosclerosis
Trial description: This study is being conducted to assess the potential anti-inflammatory effects of a 3-month treatment with GW856553, on the inflammatory activity within the aorta and carotid plaques, as assessed by FDG-PET/CT.
Primary purpose:
Treatment
Trial design:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Allocation:
Randomized
Primary outcomes:
Change from Baseline of mean of maximum tissue to background ratio (TBR) in the qualifying artery, following 12 weeks of treatment in the setting of chronic statin therapy
Timeframe: Baseline (Days -14 to -1) and up to Week 12
Secondary outcomes:
Change from Baseline of the ‘most diseased segment (MSD)’ average maximum TBR in the qualifying artery following 12 weeks of treatment with GW856553 or placebo in the setting of chronic statin therapy
Timeframe: Baseline (Days -14 to -1) and up to Week 12
Change from Baseline in blood concentration of high sensitivity C-reactive protein (hs-CRP)
Timeframe: Baseline (Day 1) and Days 7, 14, 21, 28, 42, 56, 70, 84
Mean systolic blood pressure (SBP) and diastolic blood pressure (DBP) at indicated time points
Timeframe: Day 1, 7, 14, 21, 28, 42, 56, 70, 84, 98
Mean heart rate at indicated time points
Timeframe: Day 1, 7, 14, 21, 28, 42, 56, 70, 84, 98
Number of participants with 12-lead electrocardiogram (ECG) findings
Timeframe: Days 1, 7, 14, 21, 28, 42, 56, 70, 84, 98
Number of participants with clinical chemistry abnormalities of PCI
Timeframe: Up to Follow-up (Day 98)
Number of participants with hematology abnormalities of PCI
Timeframe: Up to Follow-up (Day 98)
Number of participants with urinalysis dipstick results
Timeframe: Day 1, 7, 14, 21, 28, 42, 56, 70, 84, 98
Number of participants with Adverse Events (AEs) and Serious Adverse Events (SAEs)
Timeframe: Up to Follow-up (Day 98)
Interventions:
Drug: LOSMAPIMOD 7.5 MG
Drug: Placebo
Enrollment:
99
Observational study model:
Not applicable
Primary completion date:
2009-03-12
Time perspective:
Not applicable
Clinical publications:
Maysoon Elkhawad MA, MRCS, James H.F. Rudd PhD, MRCP, Lea Sarov-Blat PhD, Gengqian Cai, PhD, Richard Wells, BA, L. Ceri Davies MD,BBS, David Collier, PhD, Michael Marber PhD, Robin Choudury, DM, Zahi Fayad PhD, Ahmed Tawakol, MD, Fergus Gleeson, MBBS, . Effects of p38 mitogen-activated protein kinase inhibition on vascular and systemic inflammation in patients with atherosclerosis: results from a randomized controlled study. [JACC: Cardiovasc Imaging]. 2012;5(9):911-922.
Elkhawad M, Rudd JHF, Sarov-Blat L, Cai G, Wells R, Davies C, Collier D, Marber M, Choudury R, Fayad Z, Tawakol A, Gleeson F, Lapore J, Davis B, Willette RN, Wilkinson IB, Sprecher D, Cheriyan J.Effects of p38 mitogen-activated protein kinase inhibition on vascular and systemic inflammation in patients with atherosclerosis: results from a randomized controlled study.Journal of Cardiovascular Imaging.2012;5(9):911-922
Medical condition
Atherosclerosis
Product
losmapimod
Collaborators
Not applicable
Study date(s)
June 2008 to December 2009
Type
Interventional
Phase
2
Participation criteria
Sex
Female & Male
Age
50 - 80 years
Accepts healthy volunteers
No
- Inclusion Criteria for Main Study:
- 1. Adult male and female subjects, between 50 and 80 years of age, inclusive, with a body weight > 50 kg and body mass index (BMI) between 19 and 35 kg/m2
Inclusion and exclusion criteria
Inclusion criteria:
- Inclusion Criteria for Main Study: 1. Adult male and female subjects, between 50 and 80 years of age, inclusive, with a body weight > 50 kg and body mass index (BMI) between 19 and 35 kg/m2 2. Subjects who have:
- experienced a CV event (acute coronary syndrome, unstable angina, CABG, PCI, stroke, MI, TIA, carotid endarterectomy), but have been clinically stable for at least 6 months since that event,
- or, have peripheral vascular disease (PVD), as indicated by o symptoms of claudication and either a positive imaging/treadmill test, or o reduced ankle branchial pressure index,
- or, have a diagnosis of CAD corroborated by stress testing (exercise or pharmacological) or any other confirmed diagnosis of atherosclerotic arterial disease
- Individuals who have experienced a CV event or have PVD will be given preference for enrolment in the study, if they also have one of the following: o metabolic syndrome, as defined by NCEP ATP III o Framingham score > 20 o Current smokers (at least 1pack/day) o Well-controlled diabetes, defined for the purposes of this study as HbA1c <= 8%, or fasting blood glucose <= 126mg/dL (7mmol/L) 3. Subjects must be on a stable dose of statin for at least 3 months prior to first dose of study medication. Subjects must be capable of continuing statin therapy from screening until the final follow up visit. 4. Either carotid or aortic TBR ³ 1.6, as measured on FDG-PET/CT, signifying active inflammation. 5. AST and ALT < 2xULN at screening; alkaline phosphatase and bilirubin <= 1.5xULN at screening (isolated bilirubin >1.5xULN is acceptable if bilirubin is fractionated and direct bilirubin <35%). 6. A signed and dated written informed consent prior to admission to the study 7. The subject is able to understand and comply with protocol requirements, instructions and protocol-stated restrictions. Exclusion Criteria for Main Study: 1. Any medical history or clinically relevant abnormality identified on the screening medical examination, vital sign measurement, 12-lead ECG recording and/or clinical laboratory examination that is deemed by the principal investigator and/or medical monitor to make the subject ineligible for inclusion because of a safety concern. 2. History of heart failure defined as NYHA class II
- IV or those with known severe LV systolic dysfunction (EF<30%) regardless of symptomatic status 3. Subjects with atrial fibrillation (AF) at screening will be excluded. 4. Insulin controlled Type 1 or Type 2 diabetics 5. Diabetics with fasting glucose > 126mg/dL (7mmol/L) or HbAc1 levels > 8%, at screening. [note: fasting glucose to be checked again at first FDG-PET scan, and if glucose > 11mmol/L at that visit, subject will be excluded from study] 6. Positive pre-study hepatitis B surface antigen or positive hepatitis C antibody results within 3 months of screening. 7. Current or chronic history of liver disease, or known hepatic or biliary abnormalities (with the exception of Gilbert's syndrome or asymptomatic gallstones). 8. Renal impairment with creatinine clearance of <40 ml/min at screening, or history of kidney transplant or history of contrast nephropathy. 9. Subjects with rheumatoid arthritis, connective tissue disorders and other conditions known to be associated with active chronic inflammation (e.g. Inflammatory Bowel Disease). 10. Subjects with chronic infections such as HIV, gingivitis, periodonitis, prostatitis, gastritis, and urinary tract infections, or any active diseases, including active tuberculosis or a history of active tuberculosis. 11. Subjects with any acute infection, symptoms suggestive of sinusitis, or significant trauma (burns, fractures) 12. History of malignancy within the past 5 years, other than non-melanoma skin cancer. 13. History of skeletal muscle myopathy or rhabdomyolysis 14. Previous exposure to GW856553. 15. Current use of steroids (inhaled or oral) 16. Subjects who have donated more than 500 mL of blood within 56 days prior to the study medication administration. 17. Participation in a clinical study where the subject has received a drug or new chemical entity within 30 days or 5 half-lives, or twice the duration of the biological effect of the drug (whichever is longer) prior to the first dose of study medication 18. History of alcohol/drug abuse or dependence within 12 months of the study 19. The subject has a three month prior history of regular alcohol consumption exceeding an average weekly intake of >28 units (or an average daily intake of greater than 3 units) for males, or an average weekly intake of > 21 units (or an average daily intake of greater than 2 units) for females. 1 unit is equivalent to a half-pint (284mL) of beer/lager; 25mL measure of spirits or 125mL of wine; or a positive alcohol breath test at the screening visit 20. A positive urine test for drugs of abuse (not related to known medications the subject is taking, e.g. codeine for pain management) or alcohol at screening or prior to study medication administration. 21. QTc interval > 450 msec (using average value of triplicate ECGs) 22. Subjects will be excluded if they have participated in clinical research studies involving radiation in the past three years 23. Women must be of non-childbearing potential [i.e. either postmenopausal or documented hysterectomy
- Intracranial aneurysm clips (except Sugita) or other metallic objects,
- History of intra- orbital metal fragments that have not been removed by an MD,
- Pacemakers, implantable cardiac defibrillators and non-MR compatible heart valves,
- Inner ear implants,
- History of claustrophobia in MR. 2. Allergy to MRI contrast enhancement agent (gadolinium). 3. Serum creatinine clearance < 60 mL/min (At the discretion of the physician, the subject may progress to a formal assessment based on 24 hour urine collection should serum creatinine limits fall below limits.
tubal ligation is not sufficient]. For the purposes of this study, post menopausal is defined as being amenorrhoeic for greater than 2 years with an appropriate clinical profile, e.g. age appropriate, history of vasomotor symptoms. Postmenopausal status will be confirmed by serum or urine FSH and oestradiol concentrations at screening, if appropriate. Surgical sterility will be defined as females who have had a hysterectomy and/or bilateral oophorectomy. 24. An unwillingness of male subjects to abstain from sexual intercourse with pregnant or lactating women; or an unwillingness of the subject to use a condom/spermicide in addition to having their female partner use another form of contraception such as an IUD, diaphragm with spermicide, injectable progesterone, sub-dermal implants or a tubal ligation if the women could become pregnant from the time of the first dose of the study medication until 3 months after administration of last dose of study medication. Inclusion Criteria for Subjects in MRI Sub-study 1. Recent (in approximately last 12 months) echocardiogram with ejection fraction between 30 and 50%. Exclusion Criteria for Subjects in MRI Sub-study 1. Contraindication to MRI scanning (as assessed by local MRI safety questionnaire) which includes but not limited to:
Trial location(s)
Location
GSK Investigational Site
Oxford, Oxfordshire, United Kingdom, OX3 9DU
Status
Study Complete
Study documents
Clinical study report
Available language(s): English
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Results posted on ClinicalTrials.gov
Recruitment status
Completed
Actual primary completion date
2009-03-12
Actual study completion date
2009-03-12
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
Participate in clinical trial
Additional information
Researchers can use this site to request access to anonymised patient level data and/or supporting documents from clinical studies to conduct further research.
Click hereAccess to clinical trial data by researchers
Visit website