Status:
COMPLETED
Assess the Safety and Efficacy of NKPL66 (CaPre™) in the Treatment of Mild-to-high Hypertriglyceridemia
Lead Sponsor:
Grace Therapeutics Inc.
Collaborating Sponsors:
JSS Medical Research Inc.
Conditions:
Hypertriglyceridemia
Eligibility:
All Genders
18-75 years
Phase:
PHASE2
Brief Summary
To evaluate the efficacy of 0.5, 1.0, 2.0 and 4.0 g/ day of CaPre™ in reducing fasting plasma serum triglycerides over a four week period in patients with mild-to-high hypertriglyceridemia as compared...
Detailed Description
The data generated from preclinical studies, as well as data accumulated from preclinical and clinical studies conducted with the precursor of CaPre™, NKO® , a natural health product (NPN: 80006416), ...
Eligibility Criteria
Inclusion
- Male and female adults aged 18 to 75 years;
- Fasting plasma levels of TG \> 2.28 and \< 10 mmol/L (200 and 877 mg/dL) on two occasions within 2 weeks (screening and baseline/part 1 visits).
- Patients who are currently not on pharmacotherapy for hyperlipidemia and according to the judgement of the physician and Canadian Guidelines for the Diagnosis and Treatment of Dyslipidemia initiation of drug therapy is not indicated for the duration of the study.
- OR
- Patients currently treated with statins and according to the judgement of the physician and the Canadian Guidelines for the Diagnosis and Treatment of Dyslipidemia a change in their current drug regimen is not indicated for the duration of the study.
- Patients treated with statin must be on stable dose for at least 6 weeks prior to screening;
- Patients are willing to follow the NCEP Step 1 Diet (see Appendix 4) for the duration of the study;
- Female participants of childbearing potential (i.e. not surgically sterilized or post-menopausal greater than one year) must have negative serum pregnancy test and must be using an effective birth control method, defined as:
- continuous use of oral or long acting injected contraceptive for at least 2 months prior to study entry, or;
- use of an intra-uterine device or implantable contraceptive, or;
- use of double barrier methods of birth control
Exclusion
- Any concomitant medication which in the opinion of the investigator would preclude the patient from successfully participating in the study;
- Women who are pregnant or that are breast feeding;
- Participation in another clinical trial within 30 days from initiation of the study;
- Participants with a high risk for cardiovascular disease; (The definition of high-risk individuals will follow that of the 2009 Canadian Guidelines and include a) FRS \>= 20% 10-year risk; b) All patients with uncontrolled diabetes (DCA guidelines) and c) Evidence of atherosclerosis -when this evidence was ascertained when clinically indicated);
- Systolic blood pressure \> 140 mmHg and/or diastolic blood pressure \> 90 mmHg. In diabetic patients, systolic blood pressure \> 130 mmHg and/or diastolic blood pressure \> 90 mmHg.
- History of stroke, intermittent claudication or transient ischemic attack;
- Known unstable (uncontrolled) cardiac disease, within the last 6 months:
- Patient with a clinically significant abnormal ECG at screening.
- Patients with uncontrolled diabetes mellitus, with HbA1c \> 7.0%;
- Known diagnosis of hypoglycemia
- Evidence of active renal disease indicated by a fasting estimated glomerular filtration rate (eGFR) of \< 60 ml/min per 1.73 m2;
- Increased plasma levels (\>ULN) of amylase (as per respective lab upper limits) and / or lipase (\>160 IU/L) or any indication of pancreatitis (increased alcohol consumption, gallstones);
- History of pancreatitis;
- Use of any lipid lowering medication other than statins (e.g niacin, fibrates or ezetimibe) and/or lipid lowering NHP within 6 weeks prior to the screening visit;
- Intake of \> 2 servings per week of fish or regimented use of fish oil/omega-3 supplements within 6 weeks prior to the screening visit;
- Intake of fortified foods containing plant sterols within 6 weeks prior to the screening visit;
- Known HIV or Hepatitis B or C positive;
- Patients with osteoporosis and hormone sensitive conditions;
- Patients with uncontrolled asthma as defined by the 2010 Consensus Summary of the Canadian Thoracic Society;
- Known seafood allergy or allergy to any of the medicinal or non-medicinal ingredients of the study medication, including:
- Omega-3 fatty acids (including EPA and DHA)
- Phospholipids (mainly phosphatidylcholine)
- Astaxanthin
- Bovine gelatin
- Coagulopathy or on anticoagulants. Platelet aggregation inhibitors (such as aspirin or clopidogrel but not heparin) are permitted in the study; patients taking both aspirin and clopidogrel are not permitted in the study;
- Unable or unwilling to comply with the protocol;
- Patient reported weight must be stable for the past 6 months (within 3kg variation);
- Consumption of more than 14 standard alcoholic drinks a week.
Key Trial Info
Start Date :
December 1 2011
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 1 2013
Estimated Enrollment :
289 Patients enrolled
Trial Details
Trial ID
NCT01516151
Start Date
December 1 2011
End Date
September 1 2013
Last Update
January 8 2014
Active Locations (38)
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1
Alberta Health Services Clinical Trials
Red Deer, Alberta, Canada
2
Abbotsford, British Columbia, Canada
3
Kelowna, British Columbia, Canada
4
BC Diabetes
Vancouver, British Columbia, Canada