Status:
COMPLETED
Study to Test GSK256073 in Patients With Dyslipidemia
Lead Sponsor:
GlaxoSmithKline
Conditions:
Dyslipidaemias
Dyslipidemias
Eligibility:
All Genders
18-75 years
Phase:
PHASE2
Brief Summary
This is a two part study (Part A and Part B) that will first aim to establish the PK/PD relationship between exposure and lipid effects (Part A: 75 subjects), and will then confirm the effect using th...
Eligibility Criteria
Inclusion
- Signed written informed consent prior to beginning study-related procedures. Subjects must understand the aims, investigational procedures and possible consequences of the study and must be able to understand and comply with protocol requirements, instructions and protocol-stated restrictions.
- Male or female 18-75 years of age at screening.
- 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.
- Male subjects must agree to use one of several pre-specified contraception methods. This criterion must be followed from the time of the first dose of study medication until three days following the last dose.
- Body weight \> 50 kg (110 pounds) and body mass index (BMI) between 19 and 39 (inclusive)
- LDLc concentration ≥100 mg/dL at screening and within 4 weeks of randomization (if screening occurs \> 4 weeks prior to randomization)
- Fasting triglyceride concentration ≤ 300 mg/dL at screening and within 4 weeks of randomization (if screening occurs \> 4 weeks prior to randomization)
- HDLc ≤ 45 mg/dL for males or ≤ 55 mg/dL for females at screening and within 4 weeks of randomization (if screening occurs \> 4 weeks prior to randomization)
- Subject currently receiving lipid-modifying medication(s) must agree to stop medication(s) for at least 6 weeks prior to randomization. After this washout period LDL, TG and HDL values must be remeasured and meet the above criteria prior to randomization in the study
- AST and ALT \< 2xULN; alkaline phosphatase and bilirubin ≤ 1.5xULN (isolated bilirubin \>1.5xULN is acceptable if bilirubin is fractionated and direct bilirubin \<35%).
Exclusion
- Evidence of clinical instability based on a medical evaluation including medical history, physical examination, laboratory tests and cardiac monitoring. A subject with a clinical abnormality or laboratory parameter outside the reference range for the population being studied may be included only if the Investigator and the GSK Medical Monitor agree that the finding is unlikely to introduce additional risk and will not interfere with the study procedures.
- Any change in concomitant medication (including multivitamins, herbal remedies, dietary supplements, and over-the-counter medication) within six weeks prior to screening that is not approved by GSK.
- Any change in diet, exercise habits or smoking status within six weeks prior to screening.
- A medical history significant for the following:
- Clinical cardiovascular disease, including history or current evidence of coronary heart disease, heart failure, cerebrovascular disease, peripheral vascular disease, and/or a 10-year risk of CHD \> 20% while on or titrated off lipid lowering medication. Subjects pending diagnostic procedures for any of those conditions at the time of screening will not be eligible for participation.
- Renal impairment (for males) as defined by a calculated GFR \< 60 mL/min . Renal impairment (for females) as defined by a calculated GFR \< 55 ml/min.
- History of diabetes mellitus, or history of post-prandial and/or random blood glucose \> 200 mg/dl or fasting glucose \> 125 mg/dL or currently taking diabetes medications to manage fasting glucose levels (e.g. glitazones, sulfonylureas, insulin, metformin, etc.).
- History of anemia or treatment of anemia within 12 months of screening or Hgb or Hct below the lower limit of reference range for age and gender at screening
- History of pancreatitis
- Any concurrent serious illness (e.g., severe COPD, HIV positive, liver cirrhosis, history of malignancy other than skin cancer within 5 years of initial diagnosis or with evidence of recurrence) that may interfere with a subject from completing the study
- Active peptic ulcer disease (PUD) and/or history of PUD or other gastrointestinal bleeding within 12 months prior to screening.
- History of kidney stones
- History of gout and/or hyperuricemia or taking drugs for hyperuricemia: allopurinol and/or probenecid
- History of Gilbert's syndrome
- Current inadequately controlled hypertension (blood pressure ≥160 mmHg systolic or ≥100 mmHg diastolic at screening). If blood pressure medication is changed, blood pressure will be re-measured after 6 weeks and must again meet these criteria.
- An unwillingness of subjects currently taking aspirin to reduce the daily dose to 81 mg starting 2 weeks prior to first dose and until the follow-up visit.
- Creatinine phosphokinase (CPK) 2X ULN at screening.
- A serum uric acid exceeding by ≥ 15% the upper limit of the reference range at screening.
- PT and/or aPTT above the reference range.
- A positive pre-study Hepatitis B surface antigen or positive Hepatitis C antibody result within 3 months of screening.
- The subject has a positive pre-study drug screen. A minimum list of drugs that will be screened for include amphetamines, barbiturates, cocaine, opiates, cannabinoids and benzodiazepines.
- History of regular alcohol consumption within 6 months of the study defined as:
- An average weekly intake of \>14 drinks/week for men or \>7 drinks/week for women. One drink is equivalent to (12 g alcohol) = 5 ounces (150 ml) of wine or 12 ounces (360 ml) of beer or 1.5 ounces (45 ml) of 80 proof distilled spirits.
- Use of the following blood pressure medications is prohibited at any dose: enalapril, losartan, captopril
- If subjects are titrated or switched to alternative therapy they must be on a stable dose for at least 4 weeks prior to randomization.
- Subjects will be excluded if they require treatment with systemic corticosteroids
- Subjects will be excluded if they take quinolone antibiotics, methotrexate, ibuprofen or other medication secreted by renal OAT transporters
- Treatment with an investigational drug within 30 days or 5 half-lives (whichever is longer) prior to dosing
- Exposure to more than four new chemical entities within 12 months prior to the first dosing day
- History of sensitivity or untoward reaction to the study medications (i.e. GSK256073 or Niaspan), or components thereof or a history of drug or other allergy that, in the opinion of the physician responsible, contraindicates their participation
- Where participation in study would result in donation of blood in excess of 500 mL within a 56 day period.
- A positive test for HIV antibody.
- Subject is mentally or legally incapacitated.
- Unwillingness or inability to follow the procedures outlined in the protocol.
Key Trial Info
Start Date :
June 15 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
February 16 2010
Estimated Enrollment :
80 Patients enrolled
Trial Details
Trial ID
NCT00903617
Start Date
June 15 2009
End Date
February 16 2010
Last Update
December 5 2019
Active Locations (11)
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1
GSK Investigational Site
Pembroke Pines, Florida, United States, 33026
2
GSK Investigational Site
Indianapolis, Indiana, United States, 46260
3
GSK Investigational Site
Louisville, Kentucky, United States, 40213
4
GSK Investigational Site
Auburn, Maine, United States, 04210