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GSK1349572 Proton Pump Inhibitor Drug Interaction and Supratherapeutic Dose Study

Information source: GlaxoSmithKline
ClinicalTrials.gov processed this data on August 23, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Healthy Volunteer

Intervention: GSK1349572 (Drug); GSK1349572 (Drug); Placebo (Drug); Omeprazole (Drug)

Phase: Phase 1

Status: Completed

Sponsored by: GlaxoSmithKline

Official(s) and/or principal investigator(s):
GSK Clinical Trials, Study Director, Affiliation: GlaxoSmithKline

Summary

GSK1349572 is an integrase inhibitor that is currently being evaluated for the treatment of HIV infection. The primary objective of this study is to determine whether the addition of a proton pump inhibitor, omeprazole, to GSK1349572 impacts the blood levels of GSK1349572. It will also evaluate if a high fat meal impacts the blood levels of GSK1349572. In addition, the safety, tolerability, and pharmacokinetics of single supratherapeutic (high) dose of GSK1349572 will be evaluated.

Clinical Details

Official title: The Official Study Title Exceeds the 300 Character Limit for This Field. See Detailed Study Description Section for Official Study Title.

Study design: Allocation: Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Primary outcome:

Plasma GSK1349572 PK parameters following a single-dose administration of 50 mg under fasted conditions with and without omeprazole 40 mg

Plasma GSK1349572 PK parameters following a single-dose administration of 50 mg under fasted conditions and with a high-fat meal

Plasma GSK1349572 PK parameters following a single-dose administration of 250 mg under fasted conditions

Safety and tolerability parameters, including adverse event, concurrent medication, clinical laboratory, ECG, and vital signs assessments following a single supratherapeutic dose of GSK1349572 250 mg.

Secondary outcome:

Safety and tolerability parameters, including adverse event, concurrent medication, clinical laboratory, ECG, and vital signs assessments following a single-dose administration of 50 mg under fasted conditions, with a high-fat meal, and with OMP 40 mg.

Plasma GSK1349572 PK parameters following a single-dose administration of 50 mg under fasted conditions, with a high-fat meal, and with OMP 40 mg

Plasma GSK1349572 PK parameters following a single-dose administration of 250 mg under fasted conditions

Detailed description: Official Study Title: A randomized, double-blind study to evaluate the safety, tolerability, and pharmacokinetics of a supratherapeutic dose of GSK1349572 250 mg and a randomized, open-label study to evaluate the effects of omeprazole 40 mg daily and a high fat meal on the pharmacokinetics of GSK1349572 50 mg in healthy adult subjects (ING112941)

Eligibility

Minimum age: 18 Years. Maximum age: 65 Years. Gender(s): Both.

Criteria:

Inclusion Criteria:

- Healthy as determined by a responsible and experienced physician, based on a medical

evaluation including medical history, physical examination, laboratory tests and cardiac monitoring.

- Male or female between 18 and 65 years of age, inclusive.

- 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] or, Child-bearing potential and agrees to use one of the contraception methods listed in the protocol for an appropriate period of time (as determined by the product label or investigator) prior to the start of dosing to sufficiently minimize the risk of pregnancy at that point. Female subjects must agree to use contraception until 3 days after the last dose of study drug.

- Body weight ≥ 50 kg for men and ≥ 45 kg for women and BMI within the range 18. 5-31. 0

kg/m2 (inclusive).

- Capable of giving written informed consent, which includes compliance with the

requirements and restrictions listed in the consent form.

- AST, ALT, alkaline phosphatase and bilirubin ≤ 1. 5xULN (isolated bilirubin >1. 5xULN

is acceptable if bilirubin is fractionated and direct bilirubin <35%). A single repeat is allowed for eligibility determination. Exclusion Criteria:

- 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.

- 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.

- History of regular alcohol consumption within 6 months of the study defined as: an

average weekly intake of >14 drinks for males or >7 drinks for females. One drink is equivalent to 12 g alcohol: 12 ounces (360 ml) of beer, 5 ounces (150 ml) of wine or 1. 5 ounces (45 ml) of 80 proof distilled spirits.

- History of regular use of tobacco or nicotine-containing products within 3 months

prior to screening.

- 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).

- 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.

- Consumption of red wine, seville oranges, grapefruit or grapefruit juice from 7 days

prior to the first dose of study medication.

- History of sensitivity to any of the study medications, or components thereof

including sulfa-containing drugs, 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.

- Pregnant females as determined by positive serum or urine human hCG test at screening

or prior to dosing.

- Lactating females.

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

- If heparin is used during PK sampling, subjects with a history of sensitivity to

heparin or heparin-induced thrombocytopenia should not be enrolled.

- History of significant renal or hepatic diseases.

- History/evidence of clinically significant pulmonary disease.

- History/evidence of symptomatic arrhythmia, angina/ischemia, coronary artery bypass

grafting (CABG) surgery or percutaneous transluminal coronary angioplasty (PCTA) or any clinically significant cardiac disease.

- Subjects with a pre-existing condition interfering with normal gastrointestinal

anatomy or motility, hepatic and/or renal function, that could interfere with the absorption, metabolism, and/or excretion of the study drugs. Subjects with a history of cholecystectomy, inflammatory bowel disease, or pancreatitis should be excluded. Subjects with gastroesophageal reflux disease requiring the use of proton pump inhibitors or H2-blockers.

- History of upper gastrointestinal bleeding.

- Active peptic ulcer disease.

- Subjects with a hemoglobin <12 g/dL. A single repeat is allowed for eligibility

determination.

- The subject's systolic blood pressure is outside the range of 90-140mmHg, or

diastolic blood pressure is outside the range of 45-90mmHg or heart rate is outside the range of 50-100bpm for female subjects or 45-100 bpm for male subjects. A single repeat is allowed to determine subject eligibility.

- Exclusion criteria for screening ECG (a single repeat is allowed for eligibility

determination) outside of the protocol limits.

Locations and Contacts

GSK Investigational Site, Baltimore, Maryland 21225, United States
Additional Information

Starting date: July 2009
Last updated: October 8, 2009

Page last updated: August 23, 2015

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