Repeat Dose Food Effect Study of GSK256073F in Healthy Adult Subjects

Dyslipidaemias Clinical Trial

Official title:

Food Effect Study of GSK256073A in Healthy Subjects

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00808093
• Other study ID #: 106777
• Status: Completed
• Phase: Phase 1
• First received: December 11, 2008
• Last updated: June 2, 2017
• Start date: May 12, 2008
• Est. completion date: August 27, 2008

Study information

• Verified date: June 2017
• Source: GlaxoSmithKline
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to compare the effects of fasting and fed conditions with repeat doses of GSK256073F in HVT subjects.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 30
• Est. completion date: August 27, 2008
• Est. primary completion date: August 27, 2008
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

• Healthy as determined by a responsible physician, based on a medical evaluation including medical history, physical examination, laboratory tests and cardiac monitoring. A subject with a clinical abnormality or laboratory parameters 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 factors and will not interfere with the study procedures.

• Male or female of non-childbearing potential between 18 and 55 years of age.

• 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 [in questionable cases a blood sample with simultaneous follicle stimulating hormone (FSH) > 40 MlU/ml and estradiol < 40 pg/ml (<140 pmol/L) is confirmatory].

• Male subjects must agree to use one of the contraception methods listed in Section 8.1. This criterion must be followed from the time of the first dose of study medication until 3 days post-last dose.

• Body weight > 50 kg (110 pounds) and BMI within the range 19 - 31 kg/m2 (inclusive).

• Capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.

• QTcB or QTcF < 450 msec

Exclusion Criteria:

• The subject has a positive pre-study drug/alcohol screen. A minimum list of drugs that will be screened for include amphetamines, barbiturates, cocaine, opiates, cannabinoids and benzodiazepines

• A positive pre-study Hepatitis B surface antigen or positive Hepatitis C antibody result within 3 months of screening.

• A positive test for HIV antibody.

• 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.

• The subject has participated in a clinical trial and has received an investigational product within the following time period prior to the first dosing day in the current study: 30 days, 5 half-lives or twice the duration of the biological effect of the investigational product (whichever is longer).

• Exposure to more than four new chemical entities within 12 months prior to the first dosing day.

• Use of prescription or non-prescription drugs, including vitamins, herbal and dietary supplements (including St John's Wort) within 7 days (or 14 days if the drug is a potential enzyme inducer) or 5 half-lives (whichever is longer) prior to the first dose of study medication, unless in the opinion of the Investigator and GSK Medical Monitor the medication will not interfere with the study procedures or compromise subject safety. An exception is acetaminophen which is allowed at doses of = 2g/day.

• History of sensitivity to any of the study medications, or components thereof or a history of drug or other allergy that, in the opinion of the investigator or GSK Medical Monitor, contraindicates their participation.

• Where participation in the study would result in donation of blood or blood products in excess of 500 mL within a 56 day period.

• Unwillingness or inability to follow the procedures outlined in the protocol.

• Systolic blood pressure < 100 mmHg or = 150 mmHg and/or diastolic blood pressure = 100 mmHg at screening.

• History of significant cardiac arrhythmias

• Active peptic ulcer disease (PUD) and/or history of PUD within 1 year.

• Screening test positive for H. Pylori using the non-radioactive breath test.

• A serum uric acid concentration = 8mg/dL

• History of gout and/or hyperuricemia

• History of Gilbert's syndrome

• A serum creatinine concentration above the normal reference range

• History of kidney stones

• PT and/or aPTT above the reference range

• History of recurrent indigestion, stomach upset or diarrhea

• Liver function tests (LFTs) or creatinine phosphokinase (CPK) 2X ULN

• Screening stool test positive for occult blood

• Screening peripheral blood smear with abnormal RBCs

• Reduced G6PD activity

• Serum haptoglobin outside the reference range at screening

• Total serum LDH > 1.25% above the ULN at screening

• Urinary cotinine levels indicative of smoking or history or regular use of tobacco- or nicotine-containing products within 6 months prior to screening (between the normal reference range up to 200ng/mL).

• History of flushing (>1 episode annually)

• Fasting blood glucose = 110 mg/dl and/or history of type I or type II DM

• History of intra-ocular pathology, including but not limited to retinitis, uveitis, retinal detachment and macular edema

• History of recurrent gum bleeding

• History of bleeding haemorrhoids

Related Conditions & MeSH terms

• Dyslipidaemias
• Dyslipidemias

Intervention

Drug:
• GSK256073
GSK256073 100 mg study drug

Locations

Country	Name	City	State
United States	GSK Investigational Site	Baltimore	Maryland

Sponsors (1)

Lead Sponsor	Collaborator
GlaxoSmithKline

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	1. AUC0-inf, Cmax, and Ctrough (Ct) under fasting conditions		throughout study
Primary	2. AUC0-inf, Cmax, and Ctrough (Ct) under fed conditions		throughout the study
Secondary	1. Safety and tolerability will be assessed by vital signs, ECGs, clinical laboratory data, spontaneous AE reporting, nursing/physician observation and assessment of flushing via a visual analog scale		throughout the study
Secondary	2. Tmax, t½ (if data permits), Ae (amount excreted in the urine), CLr (renal clearance), Cmax, ss, and Ct following repeat dose		throughout the study
Secondary	3. Pharmacodynamic endpoints may include TC, NEFA, HDL, LDL, TG, ApoA1, ApoA2, ApoB, Lp(a), CETP, adiponectin, liposcience (particle sizing) or other markers of dyslipidemia on Days 1, 14, 21, and 28, as data permit.		throughout the study