Study to Test GSK256073 in Patients With Dyslipidemia

NCT ID: NCT00903617

Last Updated: 2019-12-05

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 80 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2009-06-15
• Study Completion Date: 2010-02-16

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 the most relevant dose(s) (Part B: ~90 subjects). Doses of 5mg, 50mg and 150mg of GSK256073 will be administered in Part A, and the dose(s) for Part B will be based on the PK/PD data from Part A. Data from Part A and Part B will be combined to decrease overall subject numbers needed in part B. Part B of the study will include a niaspan arm for relative comparison of the effects of GSK256073 and niacin on lipids and flushing

Conditions

Dyslipidaemias; Dyslipidemias

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

Part A Treatment A

5 mg of GSK256073

Group Type: EXPERIMENTAL

GSK256073

Intervention Type: DRUG

5 mg for 8 weeks

Part A Treatment B

50 mg of GSK256073

Group Type: EXPERIMENTAL

GSK256073

Intervention Type: DRUG

50 mg for 8 weeks

Part A Treatment C

150 mg of GSK256073

Group Type: EXPERIMENTAL

GSK256073

Intervention Type: DRUG

150 mg for 8 weeks

Part A Treatment D

placebo

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

placebo for 8 weeks

Part B Treatment A

placebo

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

placebo for 8 weeks

Part B Treatment B

1500 mg Niaspan

Group Type: ACTIVE_COMPARATOR

Niaspan

Intervention Type: DRUG

1500 mg for 8 weeks

Part B Treatment C

x mg dose of GSK256073 based on data from Part A

Group Type: EXPERIMENTAL

GSK256073

Intervention Type: DRUG

x mg for 8 weeks based from data from Part A

Part B Treatment D

optional dose of GSK256073 based on data from Part A

Group Type: EXPERIMENTAL

GSK256073

Intervention Type: DRUG

optional dose based on data from Part A

Interventions

GSK256073

5 mg for 8 weeks

Intervention Type: DRUG

GSK256073

50 mg for 8 weeks

Intervention Type: DRUG

GSK256073

150 mg for 8 weeks

Intervention Type: DRUG

Placebo

placebo for 8 weeks

Intervention Type: DRUG

Niaspan

1500 mg for 8 weeks

Intervention Type: DRUG

GSK256073

x mg for 8 weeks based from data from Part A

Intervention Type: DRUG

GSK256073

optional dose based on data from Part A

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• 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 Criteria

• 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.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

GlaxoSmithKline

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

GSK Clinical Trials

Role: STUDY_DIRECTOR

GlaxoSmithKline

Locations

GSK Investigational Site

Pembroke Pines, Florida, United States

GSK Investigational Site

Indianapolis, Indiana, United States

GSK Investigational Site

Louisville, Kentucky, United States

GSK Investigational Site

Auburn, Maine, United States

GSK Investigational Site

Brooklyn Center, Minnesota, United States

GSK Investigational Site

Statesville, North Carolina, United States

GSK Investigational Site

Cincinnati, Ohio, United States

GSK Investigational Site

San Antonio, Texas, United States

GSK Investigational Site

Richmond, Virginia, United States

GSK Investigational Site

Olympia, Washington, United States

GSK Investigational Site

Seattle, Washington, United States

Countries

United States

References

Olson EJ, Mahar KM, Haws TF, Fossler MJ, Gao F, de Gouville AC, Sprecher DL, Lepore JJ. A Randomized, Placebo-Controlled Trial to Assess the Effects of 8 Weeks of Administration of GSK256073, a Selective GPR109A Agonist, on High-Density Lipoprotein Cholesterol in Subjects With Dyslipidemia. Clin Pharmacol Drug Dev. 2019 Oct;8(7):871-883. doi: 10.1002/cpdd.704. Epub 2019 Jul 3.

Reference Type: BACKGROUND

PMID: 31268250 (View on PubMed)

Other Identifiers

112795

Identifier Type: -

Identifier Source: org_study_id