Last updated: 11/07/2018 07:44:41
A phase 2a study to evaluate the effect of rilapladib (SB-659032) in Alzheimer’s disease
EudraCT ID
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: A phase 2a study to evaluate the effect of rilapladib (SB-659032) on biomarkers related to the pathogenesis and progression of Alzheimer’s disease
Trial description: The study is designed to investigate the effects of rilapladib on biomarkers related to the Alzheimer’s disease, and cognitive function.
Primary purpose:
Treatment
Trial design:
Parallel Assignment
Masking:
Triple (Participant, Care Provider, Investigator)
Allocation:
Randomized
Primary outcomes:
Change from Baseline (Day 0) in cerebral spinal fluid (CSF) amyloid beta peptide (Abeta) 42 and Abeta40 at Week 24
Timeframe: Baseline (Day 0) and Week 24
Change from Baseline (Day 0) in CSF Abeta42/ Abeta40 ratio at Week 24
Timeframe: Baseline (Day 0) and Week 24
Change from Baseline (Day 0) in CSF tau and Phosphorylated tau (P-tau) measures at Week 24
Timeframe: Baseline (Day 0) and Week 24
Change from Baseline (Day 0) in the Computerized Test Battery for Cognition (CogState) battery working memory/executive function (WM/EF) composite score at Week 24
Timeframe: Baseline (Day 0) and Week 24
Secondary outcomes:
Change from Baseline (Day 0) in CSF albumin quotients at Week 24
Timeframe: Baseline (Day 0) and Week 24
Change from Baseline (Day 0) in plasma levels of Abeta42 and Abeta40 at Week 24
Timeframe: Baseline (Day 0) and Week 24
Change from Baseline (Day 0) in plasma levels of Abeta42/Abeta40 ratio at Week 24
Timeframe: Baseline (Day 0) and Week 24
Percentage Inhibition in Plasma Lipoprotein-associated phospholipase A2 (Lp-PLA2) Activity at Week 24
Timeframe: Baseline (Day 0) and Week 24
Change from Baseline (Day 0) in CogState battery overall composite score
Timeframe: Baseline (Day 0) and Week 12 (Day 84), Week 24 (Day 168)
Change from Baseline (Day 0) in CogState battery attention composite score
Timeframe: Baseline (Day 0) and Week 12 (Day 84), Week 24 (Day 168)
Interventions:
Enrollment:
124
Primary completion date:
2013-04-02
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Gareth Maher-Edwards, Jeni De’Ath, Carly Barnett, Arseniy Lavrov, Andy Lockhart. A 24-week study to evaluate the effect of rilapladib on cognition and cerebrospinal fluid biomarkers of Alzheimer's disease. Alzheimers Dement (NY). 2015;1(2):131-140
Medical condition
Alzheimer's Disease
Product
rilapladib
Collaborators
Not applicable
Study date(s)
October 2011 to February 2013
Type
Interventional
Phase
2
Participation criteria
Sex
Female & Male
Age
50 - 80 years
Accepts healthy volunteers
No
- 1. A clinical diagnosis of possible Alzheimer’s disease in accordance with the National Institute of Neurological and Communicative Diseases and Stroke/Alzheimer’s Disease and Related Disorders Association (NINCDS-ADRDA) criteria, with radiological (Magnetic Resonance Imaging [MRI] or Computed Tomography [CT]) evidence of significant cerebrovascular disease (CVD), assessed within the last 12 months
- 2. Male or female between 50 and 80 years of age inclusive, at the time of signing the informed consent.
- 1. History and/or evidence of any other CNS disorder that could be interpreted as a cause of dementia: e.g. structural or developmental abnormality, epilepsy, infectious, degenerative or inflammatory/demyelinating CNS conditions such as, Parkinson’s disease and frontotemporal dementia
- 2. History of significant psychiatric illness such as schizophrenia or bipolar affective disorder that in the opinion of the Investigator would interfere with participation in the study; major depressive disorder (according to DSM-IV) in the past year; current active depression requiring initiation of treatment (or is believed to account for substantial degree of cognitive impairment)
Inclusion and exclusion criteria
Inclusion criteria:
- 1. A clinical diagnosis of possible Alzheimer’s disease in accordance with the National Institute of Neurological and Communicative Diseases and Stroke/Alzheimer’s Disease and Related Disorders Association (NINCDS-ADRDA) criteria, with radiological (Magnetic Resonance Imaging [MRI] or Computed Tomography [CT]) evidence of significant cerebrovascular disease (CVD), assessed within the last 12 months 2. Male or female between 50 and 80 years of age inclusive, at the time of signing the informed consent. 3. Subject has a documented history of at least 6 months of ongoing Alzheimer's disease therapy (AChEIs and/or memantine) with stable dosing for at least the last 2 months (and with no intent to change for the duration of the study). 4. Mini-Mental Status Examination (MMSE) score between 20 and 26 at Screening. 5. Clinical Dementia Rating Scale (CDR) score of 0.5 or 1.0 at Screening. 6. A female subject is eligible to participate if she is of non-childbearing potential defined as pre-menopausal females with a documented tubal ligation or hysterectomy; or postmenopausal defined as 12 months of spontaneous amenorrhea; or of child-bearing potential and agrees to use acceptable contraception methods 7. Subject has provided full written informed consent prior to the performance of any protocol-specified procedure; or if the subject is unable to provide informed consent due to cognitive status, the subject will provide assent and full written informed consent will be provided by a legally acceptable representative 8. The subject has a dedicated caregiver who is willing to supervise participation in the study 9. In the opinion of the investigator, the subject has the ability to comply with study procedures (cognitive and other testing) and is fluent in the language used for the administration of the cognitive tests.
Exclusion criteria:
- 1. History and/or evidence of any other CNS disorder that could be interpreted as a cause of dementia: e.g. structural or developmental abnormality, epilepsy, infectious, degenerative or inflammatory/demyelinating CNS conditions such as, Parkinson’s disease and frontotemporal dementia 2. History of significant psychiatric illness such as schizophrenia or bipolar affective disorder that in the opinion of the Investigator would interfere with participation in the study; major depressive disorder (according to DSM-IV) in the past year; current active depression requiring initiation of treatment (or is believed to account for substantial degree of cognitive impairment) 3. Evidence of the following disorders: current vitamin B12 deficiency, positive syphilis serology (unless neurosyphilis was ruled out) or active thyroid dysfunction (particularly suggestive of hypothyroidism), including abnormally high or low serum levels of thyroid stimulating hormone (TSH), where this is thought to be the cause of, or to contribute to the severity of the subject's dementia. 4. History of alcohol or other substance abuse, according to the DSM-IV criteria, or recent or remote history of the same if that could be a contributing factor to dementia. 5. History of intra cerebral haemorrhage due to any of the following causes: cerebral amyloid angiopathy, uncontrolled hypertension, cerebral arteriovenous malformation, coagulopathy, CNS vasculitis or any other condition that the investigator and/or medical monitor considers as a relevant risk factor for intracerebral haemorrhage 6. Recent (i.e.,<6 months from Screening Visit) cardiovascular event defined as: a. ST-elevation MI or non-ST-elevation MI, confirmed by cardiac enzyme elevation and ECG changes b. coronary revascularization (percutaneous coronary intervention or coronary artery bypass graft ) c. stroke of any etiology d. resuscitated sudden death e. prior carotid surgery or stenting procedure 7. Poorly controlled hypertension despite lifestyle modifications and pharmacotherapy (either systolic blood pressure >160mmHg or diastolic blood pressure >110mmHg) 8. QTcB interval >450 msec; or QTcB > 480 msec in subjects with bundle branch block based on ECG assessment at the Screening visit. 9. HbA1c >12.0 at Screening, or uncontrolled diabetes in the opinion of the investigator. 10. History of glaucoma or any other findings in the baseline eye exam that, in the opinion of the investigator, would exclude the subject from participation in the study. 11. History of adult asthma (or reactive airway disease) manifested by bronchospasm in the past 6 months, or currently taking regular anti-asthmatic medication(s). 12. Previous history of anaphylaxis, severe allergic reaction or history of hypersensitivity to any of the components of the formulation. 13. Significant abnormalities on clinical chemistry, haematology or urinalysis at Screening, including clinically significant anaemia. 14. History of chronic viral hepatitis (including presence of B surface antigen or hepatitis C antibody), or other chronic hepatic disorders. 15. Abnormal Screening blood tests exceeding any of the limits defined below: a. Alanine transaminase (ALT) or aspartate transaminase (AST) >1.5 x the upper limit of normal (ULN) b. Alkaline phosphatase (AP) and bilirubin >1.5X ULN (isolated bilirubin >1.5x ULN is acceptable if bilirubin is fractionated and direct bilirubin <35%). c. Calculated creatinine clearance < 30 ml/min (per Cockcroft & Gault) at Screening 16. Other clinically significant abnormality on physical (including neurological), laboratory or ECG examination that could be detrimental to the subject in the opinion of the Investigator or could compromise the integrity of the study. 17. Planned major surgery within the study period. 18. Use of systemic steroids or other immunosuppressants within the last 30 days prior to screening. 19. Current treatment with barbiturates, MAO inhibitors, butyrophenones, phenothiazines and other “conventional” antipsychotic within 30 days or 5 half-lives prior to Screening, whichever is longer. 20. Treatment with antidepressants, (other than MAO inhibitors), thyroid hormones, atypical antipsychotics (e.g. risperidone), benzodiazepines and other sedatives / hypnotics unless prescribed at a stable dose for at least 2 months prior to Screening. Note: Benzodiazepines or other sedatives/hypnotics (including antihistamines) with half-life less than 6 hours can be taken on a prn (as needed) basis but must not be taken within 5 half lives prior to cognitive testing. 21. Current treatment with known potent inhibitors of CYP3A4 (e.g. ketoconazole, rifampin, modafinil). 22. Current treatment with known potent Pgp inhibitors (itraconazole, ketoconazole, cyclosporin, loperamide, diltiazem, verapamil, spironolactone, quinidine, bepridil, quinine, carvedilol) 23. Cognitive tasks prescribed for cognitive rehabilitation and performed under medical supervision in the 6 months prior to screening and/or during study 24. Investigational medications or devices including symptomatic AD treatment during the 60 days prior to the Screening visit, or within 5 half-lives of use of the investigational drug prior to the Screening Visit, whichever is longer. 25. Participation in another investigational drug (with the exception of anti-amyloid monoclonal antibodies [mAbs]) or device study where subject was treated chronically (i.e. > 1 single dose) with a study agent intended to impact AD progression during the 12 months prior to the Screening visit. a. Subjects who participated in an investigational drug study that involved chronic dosing with a monoclonal antibody at any time in the past are excluded from this study, unless it is known that they received placebo during the previous study. b. Subjects who participated in previous single-dose studies of anti-amyloid mAbs will be permitted provided the subject’s dose of the mAb is at least 5 half-lives removed; the subjects did not experience any moderate adverse events classified as possibly drug-related or any serious adverse event during that study; the subject did not drop out of the previous study (i.e. completed all safety assessments) 26. Subjects, who in the investigator's judgement, pose a significant suicide risk (e.g. history of suicidal behaviour in the last 6 months and/or any suicidal ideation of type 4 or 5 on the C-SSRS in the last 2 months). 27. Subject or caregiver is an immediate family member or employee of the participating Investigator, any of the participating site staff or GSK staff. 28. Any contraindication to lumbar puncture or insertion of CSF catheter, including but not limited to a. Thrombocytopenia or other coagulation disorders (including subjects receiving coumarin-derived anti-coagulants or low-molecular-weight heparin). b. The presence of cutaneous or soft tissue infection overlying or adjacent to the site of lumbar puncture. c. Previous spinal surgery that could complicate access to the subarachnoid space. d. Suspicion of increased intracranial pressure due to a cerebral mass.
Trial location(s)
Location
GSK Investigational Site
Ulm, Baden-Wuerttemberg, Germany, 89081
Status
Study Complete
Location
GSK Investigational Site
Koeln, Nordrhein-Westfalen, Germany, 50935
Status
Study Complete
Location
GSK Investigational Site
Ellwangen, Baden-Wuerttemberg, Germany, 73479
Status
Study Complete
Showing 1 - 6 of 30 Results
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
Study complete
Actual primary completion date
2013-04-02
Actual study completion date
2013-18-02
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