- ICH GCP
- Register voor klinische proeven in de VS.
- Klinische proef NCT01831804
Safety, Tolerability, Pharmacokinetics and Pharmacodynamics Study of Single and Repeated Doses of Topical GSK1278863
28 juni 2019 bijgewerkt door: GlaxoSmithKline
Phase I Trial to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single Doses of Topical GSK1278863 in Healthy Volunteers and Diabetic Patients, and Repeat Doses of GSK1278863 in Diabetic Patients for the Treatment of Diabetic Foot Ulcer
This is a randomized, placebo-controlled, single-blind (subjects and investigators will be blinded, GSK internal personnel will not be blinded), parallel-group, two part (Part A, Part B) trial in healthy volunteers and subjects with diabetic foot ulcers.
Part A is designed to evaluate single applications of GSK1278863 in one cohort of healthy volunteers (intact skin) and approximately 3 cohorts of diabetic subjects.
Part B is designed to evaluate first single, and then repeat applications of GSK1278863 in diabetics, both in the clinic and by subjects at home.
Part B will include approximately 3 cohorts in which the concentration of drug applied will be determined by pharmacokinetic data from Part A and earlier cohorts in Part B.
Studie Overzicht
Toestand
Voltooid
Conditie
Interventie / Behandeling
Studietype
Ingrijpend
Inschrijving (Werkelijk)
65
Fase
- Fase 1
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studie Locaties
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California
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Castro Valley, California, Verenigde Staten, 94546
- GSK Investigational Site
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District of Columbia
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Washington, District of Columbia, Verenigde Staten, 20007
- GSK Investigational Site
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Florida
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Miami, Florida, Verenigde Staten, 33176
- GSK Investigational Site
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Pinellas Park, Florida, Verenigde Staten, 33782
- GSK Investigational Site
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Nevada
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Las Vegas, Nevada, Verenigde Staten, 89106
- GSK Investigational Site
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Rhode Island
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Providence, Rhode Island, Verenigde Staten, 02903
- GSK Investigational Site
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Texas
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Dallas, Texas, Verenigde Staten, 75390
- GSK Investigational Site
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Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
18 jaar tot 90 jaar (Volwassen, Oudere volwassene)
Accepteert gezonde vrijwilligers
Nee
Geslachten die in aanmerking komen voor studie
Allemaal
Beschrijving
Inclusion Criteria - Healthy Volunteers (Part A Cohort 1)
- Alanine aminotransferase (ALT), alkaline phosphatase and bilirubin <=1.5xupper limit of normal (ULN) (isolated bilirubin >1.5xULN is acceptable if bilirubin is fractionated and direct bilirubin <35%).
- [Single] corrected QT interval (QTc) < 450 millisecond (msec).
- Healthy as determined by a responsible and experienced physician, based on a medical evaluation including medical history, physical examination, laboratory tests and electrocardiogram (ECGs). 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 GlaxoSmithKline (GSK) Medical Monitor agree that the finding is unlikely to introduce additional risk factors and will not interfere with the study procedures. Subjects with hemoglobin (Hb) values higher than ULN the normal range should always be excluded from enrollment.
- Male or female between 18 and 90 years of age inclusive, at the time of signing the informed consent.
- A female subject is eligible to participate if she is of non-childbearing potential (postmenopausal or pre-menopausal females with a documented tubal ligation or hysterectomy). Females on hormone replacement therapy (HRT) and whose menopausal status is in doubt will be required to use one of the contraception methods in the protocol.
- Male subjects with female partners of child-bearing potential must agree to use one of the contraception methods listed in the protocol.
Inclusion Criteria - DFU Subjects must meet healthy volunteer inclusion criteria and the following
- Diagnosed with Type I or Type II diabetes mellitus.
- Glycosylated haemoglobin (HbA1c) <=12%.
- QTc < 480 msec in subjects with bundle branch block.
- Lower extremity diabetic foot ulcer of 30 to 364 days' duration.
- DFU between 1 centimeter squared (cm ^2) and 20 cm^2 at screening.
- Presence of at least one DFU that meets all of the following criteria: (a). Ulcer has been diagnosed as a full-thickness, neuropathic DFU and is located at or distal to the malleolus (excluding ulcers between the toes but including those of the heel). (b). There is a minimum 2 cm margin between the qualifying study ulcer and any other ulcers on the specified foot. (c). Ulcer size (area) >=1 cm^2 and <=12 cm^2 (post-debridement at time of randomization). (d). Wagner Grade 1. (e). Depth <=5 millimeter (mm) with no capsule, tendon or bone exposed and no tunneling, undermining, or sinus tracts. Note: If the subject has more than one qualifying DFU, the ulcer designated as the study ulcer will be at the discretion of the Investigator. Non-study ulcers being treated during the course of the study will be treated with moist wound therapy Standard of Care (SOC) identified under this study.
- Adequate vascular perfusion of the affected limb within 30 days of screening, as defined by at least one of the following: (a) Transcutaneous oxygen partial pressure (TcPO2) >35 millimeter of mercury (mmHg). (b) Ankle-Brachial Index (ABI) >=0.6 and <=1.2, confirmed by TcPO2 >35 mmHg. (c) Toe pressure (plethysmography) >50 mmHg. (d) Doppler ultrasound (biphasic or triphasic waveforms) consistent with adequate blood flow to the affected extremity, as determined by SOC.
Exclusion Criteria - Healthy Volunteers (Part A Cohort 1)
- A positive pre-study Hepatitis B surface antigen or positive Hepatitis C antibody result within 3 months of screening.
- Current or chronic history of liver disease, or known hepatic or biliary abnormalities (with the exception of Gilbert's syndrome or asymptomatic gallstones).
- History of malignancy within 5 years of Screening or those with a strong family history of cancer (e.g., familial cancer disorders), with the exception of squamous cell or basal cell carcinoma of the skin that has been definitively treated.
- A history of drug or alcohol abuse, or a 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 gram of alcohol: 12 ounces (360 mililiter [mL]) of beer, 5 ounces (150 mL) of wine or 1.5 ounces (45 mL) of 80 proof distilled spirits.
- A positive test for human immunodeficiency virus (HIV) antibody.
- 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 (whichever is longer).
- Unable to refrain from the 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 GlaxoSmithKline (GSK) Medical Monitor the medication will not interfere with the study procedures or compromise subject safety.
- 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 500mL within a 56 day period.
- Pregnant females as determined by positive urine human chorionic gonadotropin test at screening or prior to dosing.
- Unwillingness or inability to follow the procedures outlined in the protocol.
- Subject is mentally or legally incapacitated. Exclusion Criteria - DFU Subjects
Healthy volunteer exclusions apply to DFU subjects in addition to the following:
- Subjects with ulcers accompanied by infected cellulitis, osteomyelitis, or clinical signs or symptoms of infection, Gangrene on any part of affected limb, Active Charcot's foot on the study limb, Planned vascular surgery, angioplasty or thrombolysis, Ulcers involving exposure of tendon, bone, or joint capsule (It is acceptable to have ulcers extending through the dermis and into subcutaneous tissue with presence of granulation tissue), Ulcers due to non-diabetic etiology.
- Any unstable vascular syndromes (such as transient ischemic attack (TIA), cerebrovascular accident (CVA), unstable angina, acute myocardial infarction (MI) or acute coronary syndrome event (ACS) and/or any major changes (per investigator's judgment) to related medications within 6 months prior to randomization.
- History or malignancy within 5 years of screening or those with a strong family history of cancer (e.g. familial cancer disorders), with the exception of squamous cell or basal cell carcinoma of the skin that has been definitively treated.
- Other clinically significant cardiovascular, pulmonary, renal, endocrine, hepatic, neurological, psychiatric, immunological, gastrointestinal, hematological, or metabolic disease that is, in the opinion of the Investigator or the GSK Medical Monitor, not stabilized or may otherwise impact the results of the study.
- Patients with active treatment for retinal neovascularization (e.g., diabetic proliferative retinopathy or age related macular degeneration) within 6 months of randomization.
- Patients undergoing hemodialysis.
- History of venous thrombosis defined as deep vein thrombosis, pulmonary embolism or other venous thrombotic condition within 1 year prior to screening.
- Active peptic, duodenal, or esophageal ulcer disease or any gastrointestinal bleeding, within 1 year prior to screening.
- Subjects with a platelet count <100,000/mm^3 at screening.
- Subjects with an International Normalized Ratio (INR) >1.5 at screening.
- Subjects with a hemoglobin level above the gender-specific upper limit of normal at screening.
- Subjects with a history of non-traumatic joint inflammation (with the exception of inflammation due to osteoarthritis).
- Patients with known pulmonary hypertension.
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Enkel
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
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Experimenteel: Cohort 1 Part A
Healthy subjects in this arm will receive single applications of GSK1278863 or placebo (with 6:2 ratio) on intact skin in two escalating dosing periods each separated by 10 days.
The first application will be with a single dose of 0.3 mg and second application will be single dose of 3 mg.
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White to off-white smooth ointment with unit dose strength of 0.05%w/w, 0.1%w/w, 0.5%w/w, 1.0%w/w for topical application as single or repeat doses.
White to off-white smooth ointment for topical application as single or repeat doses.
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Experimenteel: Cohort 2 Part A
Subjects with diabetic foot ulcer (DFU) will receive a single application of GSK1278863 or placebo (with 6:2 ratio) in two dosing periods separated by 10 days.
The first application will be made on intact skin and second application directly on DFU.
Dose will be based on wound area and review from previous cohort data.
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White to off-white smooth ointment with unit dose strength of 0.05%w/w, 0.1%w/w, 0.5%w/w, 1.0%w/w for topical application as single or repeat doses.
White to off-white smooth ointment for topical application as single or repeat doses.
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Experimenteel: Cohort 3 Part A
Subjects with DFU will receive single application of GSK1278863 or placebo directly on DFU.
Dose will be based on wound area and review from previous cohort data.
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White to off-white smooth ointment with unit dose strength of 0.05%w/w, 0.1%w/w, 0.5%w/w, 1.0%w/w for topical application as single or repeat doses.
White to off-white smooth ointment for topical application as single or repeat doses.
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Experimenteel: Cohort 4 Part A
Subjects with DFU will receive a single application of GSK1278863 or placebo (with 6:2 ratio) in two dosing periods separated by 10 days.
The first application will be made on DFU and second application on intact skin.
Dose will be based on wound area and review from previous cohort data.
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White to off-white smooth ointment with unit dose strength of 0.05%w/w, 0.1%w/w, 0.5%w/w, 1.0%w/w for topical application as single or repeat doses.
White to off-white smooth ointment for topical application as single or repeat doses.
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Experimenteel: Cohort 5 Part B
Subjects with DFU will receive Standard of care (SOC) up to 15 days and then will be randomized to one of the three arms: GSK1278863 + SOC, or SOC only, or placebo + SOC with ratio of 12:2:2.
Doses for the cohorts in Part B will be determined from safety, tolerability and PK data from Part A. subjects will first be given a single application of GSK1278863 or placebo at the dose chosen for that cohort, followed by a 7-day washout period, and then repeat applications for 14 days, starting on Day 8.
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White to off-white smooth ointment with unit dose strength of 0.05%w/w, 0.1%w/w, 0.5%w/w, 1.0%w/w for topical application as single or repeat doses.
White to off-white smooth ointment for topical application as single or repeat doses.
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Experimenteel: Cohort 6 Part B
Subjects with DFU will receive Standard of care (SOC) up to 15 days and then will be randomized to one of the three arms: GSK1278863 + SOC, or SOC only, or placebo + SOC with ratio of 12:2:2.
Doses for the cohorts in Part B will be determined from safety, tolerability and PK data from Part A. subjects will first be given a single application of GSK1278863 or placebo at the dose chosen for that cohort, followed by a 7-day washout period, and then repeat applications for 14 days, starting on Day 8.
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White to off-white smooth ointment with unit dose strength of 0.05%w/w, 0.1%w/w, 0.5%w/w, 1.0%w/w for topical application as single or repeat doses.
White to off-white smooth ointment for topical application as single or repeat doses.
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Experimenteel: Cohort 7 Part B
Subjects with DFU will receive Standard of care (SOC) up to 15 days and then will be randomized to one of the three arms: GSK1278863 + SOC, or SOC only, or placebo + SOC with ratio of 12:2:2.
Doses for the cohorts in Part B will be determined from safety, tolerability and PK data from Part A. subjects will first be given a single application of GSK1278863 or placebo at the dose chosen for that cohort, followed by a 7-day washout period, and then repeat applications for 14 days, starting on Day 8.
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White to off-white smooth ointment with unit dose strength of 0.05%w/w, 0.1%w/w, 0.5%w/w, 1.0%w/w for topical application as single or repeat doses.
White to off-white smooth ointment for topical application as single or repeat doses.
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
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Number of Participants With Adverse Events (AEs) and Serious Adverse Events (SAEs) Following Single Dose Administration (Part A)
Tijdsspanne: Up to a maximum of 75 days (Start of study treatment through final follow up 2 [28-32 days post last dose])
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An AE is any untoward medical occurrence in a clinical investigation participant, temporally associated with the use of a medicinal product, whether or not considered related to the medicinal product.
An SAE is any untoward medical occurrence that, at any dose: results in death; is life-threatening; requires hospitalization or prolongation of existing hospitalization; results in disability/incapacity; is a congenital anomaly/birth defect; other important medical events; or is associated with liver injury and impaired liver function.
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Up to a maximum of 75 days (Start of study treatment through final follow up 2 [28-32 days post last dose])
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Number of Participants With AEs and SAEs Following Repeat Dose Administration (Part B)
Tijdsspanne: Up to a maximum of 53 days (Start of study treatment through final follow up 2 [28-32 days post last dose])
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An AE is any untoward medical occurrence in a clinical investigation participant, temporally associated with the use of a medicinal product, whether or not considered related to the medicinal product.
An SAE is any untoward medical occurrence that, at any dose: results in death; is life-threatening; requires hospitalization or prolongation of existing hospitalization; results in disability/incapacity; is a congenital anomaly/birth defect; other important medical events; or is associated with liver injury and impaired liver function.
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Up to a maximum of 53 days (Start of study treatment through final follow up 2 [28-32 days post last dose])
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Number of Participants With Clinically Significant 12-lead Electrocardiograms (ECGs) Measurement Following Single Dose Administrations (Part A)
Tijdsspanne: Up to a maximum of 75 days (Start of study treatment through final follow up 2 [28-32 days post last dose])
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ECG measurements were taken with the participants in supine position for at least 5 minutes.
The number of participants with clinically significant abnormal ECG measurement following single dose administration for worst case post-Baseline visit has been presented.
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Up to a maximum of 75 days (Start of study treatment through final follow up 2 [28-32 days post last dose])
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Number of Participants With Clinically Significant 12-lead ECG Measurement Following Repeat Dose Administrations (Part B)
Tijdsspanne: Up to a maximum of 53 days (Start of study treatment through final follow up 2 [28-32 days post last dose])
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ECG measurements were taken with the participants in supine position for at least 5 minutes.
The number of participants with clinically significant abnormal ECG measurement following single dose administration for worst case post-Baseline visit has been presented.
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Up to a maximum of 53 days (Start of study treatment through final follow up 2 [28-32 days post last dose])
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Number of Participants With Vital Sign Data Outside Clinical Concern Range Following Single Dose Administration (Part A)
Tijdsspanne: Day 1 (pre-dose and 48 hours) of Periods 1 and 2
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Vital sign measurements included systolic blood pressure (SBP) and diastolic blood pressure (DBP).
Vital signs were measured after the participants rested in a supine or semi-supine position for 5 minutes prior to the procedure.
Only those participants with data available at the specified data points were analyzed (represented by n= X in the category titles).
When a high or low value was reported, all values are presented for that time point and parameter.
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Day 1 (pre-dose and 48 hours) of Periods 1 and 2
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Number of Participants With Vital Sign Data Outside Clinical Concern Range Following Repeat Dose Administration (Part B)
Tijdsspanne: Days 1 and 7 (pre-dose), Day 14 (24 hours)
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Vital sign measurements included systolic blood pressure (SBP) and diastolic blood pressure (DBP).
Vital signs were measured after the participants rested in a supine or semi-supine position for 5 minutes prior to the procedure.
Only those participants with data available at the specified data points were analyzed (represented by n= X in the category titles).
When a high or low value was reported, all values are presented for that time point and parameter.
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Days 1 and 7 (pre-dose), Day 14 (24 hours)
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Number of Participants With Abnormal Nurse/Physician Observation (Part A)
Tijdsspanne: Up to a maximum of 75 days (Start of study treatment through final follow up 2 [28-32 days post last dose])
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A brief physical assessments of the skin, lungs, cardiovascular system, and abdomen (liver and spleen) were planned to be performed by qualified licensed, medical professional (i.e., physician, physician assistant, or nurse practitioner) but was not performed.Since data was not collected, no analysis was performed.
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Up to a maximum of 75 days (Start of study treatment through final follow up 2 [28-32 days post last dose])
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Number of Participants With Abnormal Nurse/Physician Observation (Part B)
Tijdsspanne: Up to a maximum of 53 days (Start of study treatment through final follow up 2 [28-32 days post last dose])
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A brief physical assessments of the skin, lungs, cardiovascular system, and abdomen (liver and spleen) were planned to be performed by qualified licensed, medical professional (i.e., physician, physician assistant, or nurse practitioner) but was not performed.
Since data was not collected, no analysis was performed.
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Up to a maximum of 53 days (Start of study treatment through final follow up 2 [28-32 days post last dose])
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Number of Participants With Hematology Values Outside the Clinical Concern Range (Part A)
Tijdsspanne: Day 1 (pre-dose)
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Hematology parameters assessed were: platelet count, red blood cell count, white blood cell count, hemoglobin, reticulocyte count, hematocrit, absolute neutrophil count (ANC), monocytes, lymphocytes, eosinophils, basophils, mean corpuscular volume, mean corpuscular hemoglobin, and mean corpuscular hemoglobin concentration.
When a high or low value was reported, all values are presented for that time point and parameter.
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Day 1 (pre-dose)
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Number of Participants With Hematology Data Outside the Clinical Concern Range (Part B)
Tijdsspanne: Day 1 (pre-dose)
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Hematology parameters assessed were: platelet count, red blood cell count, white blood cell count, hemoglobin, reticulocyte count, hematocrit, neutrophils, monocytes, lymphocytes, eosinophils, basophils, mean corpuscular volume, mean corpuscular hemoglobin, and mean corpuscular hemoglobin concentration.
When a high or low value was reported, all values are presented for that time point and parameter.
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Day 1 (pre-dose)
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Number of Participants With Clinical Chemistry Values Outside the Clinical Concern Range (Part A)
Tijdsspanne: Day 1 (pre-dose and 48 hours) in period 1; Day 1 (48 hours) in period 2
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Chemistry parameters assessed were: Blood urea nitrogen (BUN), creatinine, fasting glucose, sodium, creatine phosphokinase (CPK), potassium, chloride, total carbon dioxide (CO2), calcium, glycosylated hemoglobin (HbA1C), Aspartate aminotransferase (AST), Alanine aminotransferase (ALT), Gamma glutamyltransferase (GGT), Alkaline phosphatase (ALP), High sensitivity C-reactive protein (hsCRP), total and direct bilirubin, uric acid, albumin and total protein.
Only those participants with data available at the specified data points were analyzed (represented by n= X in the category titles).
When a high or low value was reported, all values are presented for that time point and parameter.
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Day 1 (pre-dose and 48 hours) in period 1; Day 1 (48 hours) in period 2
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Number of Participants With Clinical Chemistry Values Outside the Clinical Concern Range (Part B)
Tijdsspanne: Days 1 and 7 (pre-dose) and Day 14 (24 hours)
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Chemistry parameters assessed were: Blood urea nitrogen (BUN), creatinine, fasting glucose, sodium, creatine phosphokinase (CPK), potassium, chloride, total carbon dioxide (CO2), calcium, glycosylated hemoglobin (HbA1C), Aspartate aminotransferase (AST), Alanine aminotransferase (ALT), Gamma glutamyltransferase (GGT), Alkaline phosphatase (ALP), High sensitivity C-reactive protein (hsCRP), total and direct bilirubin, uric acid, albumin and total protein.
Only those participants with data available at the specified data points were analyzed (represented by n= X in the category titles).
When a high or low value was reported, all values are presented for that time point and parameter.
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Days 1 and 7 (pre-dose) and Day 14 (24 hours)
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Maximum Observed Concentration (Cmax) of GSK1278863 (Part A)
Tijdsspanne: Pre-dose and 0.25, 0.5, 1, 2, 4, 8, 12, 24, 48 and 72 hrs post-dose
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The pharmacokinetic (PK) parameters were calculated by standard non-compartmental analysis according to current working practices and using WinNonlin Version 5.2 or higher.
All calculations of non-compartmental parameters were based on actual sampling times.
Cmax could not be determined as data was below the limit of quantification.
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Pre-dose and 0.25, 0.5, 1, 2, 4, 8, 12, 24, 48 and 72 hrs post-dose
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Cmax of GSK1278863 (Part B)
Tijdsspanne: Pre-dose and 2 hrs on Day 1 and 7; pre-dose, 1, 2,4, 8, 12 and 24 hrs post-dose on Day 14
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The pharmacokinetic parameters were calculated by standard non-compartmental analysis according to current working practices and using WinNonlin Version 5.2 or higher.
All calculations of non-compartmental parameters were based on actual sampling times.
Cmax could not be determined as data was below the limit of quantification.
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Pre-dose and 2 hrs on Day 1 and 7; pre-dose, 1, 2,4, 8, 12 and 24 hrs post-dose on Day 14
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Time of Occurrence of Cmax (Tmax) of GSK1278863 (Part A)
Tijdsspanne: Pre-dose and 0.25, 0.5, 1, 2, 4, 8, 12, 24, 48 and 72hrs post-dose
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The pharmacokinetic parameters were calculated by standard non-compartmental analysis according to current working practices and using WinNonlin Version 5.2 or higher.
All calculations of non-compartmental parameters were based on actual sampling times.
Tmax could not be determined as data was below the limit of quantification.
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Pre-dose and 0.25, 0.5, 1, 2, 4, 8, 12, 24, 48 and 72hrs post-dose
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Tmax of GSK1278863 (Part B)
Tijdsspanne: Pre-dose and 2 hrs on Day 1 and 7; pre-dose, 1, 2,4, 8, 12 and 24 hrs post-dose on Day 14
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The pharmacokinetic parameters were calculated by standard non-compartmental analysis according to current working practices and using WinNonlin Version 5.2 or higher.
All calculations of non-compartmental parameters were based on actual sampling times.
Tmax could not be determined as data was below the limit of quantification.
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Pre-dose and 2 hrs on Day 1 and 7; pre-dose, 1, 2,4, 8, 12 and 24 hrs post-dose on Day 14
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Apparent Terminal Elimination Half-life (t1/2) of GSK1278863 (Part A)
Tijdsspanne: Pre-dose and 0.25, 0.5, 1, 2, 4, 8, 12, 24, 48 and 72hrs post-dose
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The pharmacokinetic parameters were calculated by standard non-compartmental analysis according to current working practices and using WinNonlin Version 5.2 or higher.
All calculations of non-compartmental parameters were based on actual sampling times.
t1/2 could not be determined as data was below the limit of quantification.
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Pre-dose and 0.25, 0.5, 1, 2, 4, 8, 12, 24, 48 and 72hrs post-dose
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t1/2 of GSK1278863 (Part B)
Tijdsspanne: Pre-dose and 2 hrs on Day 1 and 7; pre-dose, 1, 2,4, 8, 12 and 24 hrs post-dose on Day 14
|
The pharmacokinetic parameters were calculated by standard non-compartmental analysis according to current working practices and using WinNonlin Version 5.2 or higher.
All calculations of non-compartmental parameters were based on actual sampling times.
t1/2 could not be determined as data was below the limit of quantification.
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Pre-dose and 2 hrs on Day 1 and 7; pre-dose, 1, 2,4, 8, 12 and 24 hrs post-dose on Day 14
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Lag Time Before Observation of Drug Concentrations in Sampled Matrix (Tlag) (Part A)
Tijdsspanne: Pre-dose and 0.25, 0.5, 1, 2, 4, 8, 12, 24, 48 and 72hrs post-dose
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The pharmacokinetic parameters were calculated by standard non-compartmental analysis according to current working practices and using WinNonlin Version 5.2 or higher.
All calculations of non-compartmental parameters were based on actual sampling times.
Tlag could not be determined as data was below the limit of quantification.
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Pre-dose and 0.25, 0.5, 1, 2, 4, 8, 12, 24, 48 and 72hrs post-dose
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Lag Time Before Observation of Drug Concentrations in Sampled Matrix (Tlag) (Part B)
Tijdsspanne: Pre-dose and 2 hrs on Day 1 and 7; pre-dose, 1, 2,4, 8, 12 and 24 hrs post-dose on Day 14
|
The pharmacokinetic parameters were calculated by standard non-compartmental analysis according to current working practices and using WinNonlin Version 5.2 or higher.
All calculations of non-compartmental parameters were based on actual sampling times.
Tlag could not be determined as data was below the limit of quantification.
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Pre-dose and 2 hrs on Day 1 and 7; pre-dose, 1, 2,4, 8, 12 and 24 hrs post-dose on Day 14
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Area Under the Concentration-time Curve From Time Zero (Pre-dose) Extrapolated to Infinite Time [AUC(0-inf)] of GSK1278863 (Part A)
Tijdsspanne: Pre-dose and 0.25, 0.5, 1, 2, 4, 8, 12, 24, 48 and 72hrs post-dose
|
The pharmacokinetic parameters were calculated by standard non-compartmental analysis according to current working practices and using WinNonlin Version 5.2 or higher.
All calculations of non-compartmental parameters were based on actual sampling times.
AUC (0-inf) could not be determined as data was below the limit of quantification.
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Pre-dose and 0.25, 0.5, 1, 2, 4, 8, 12, 24, 48 and 72hrs post-dose
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AUC(0-inf) of GSK1278863 (Part B)
Tijdsspanne: Pre-dose and 2 hrs on Day 1 and 7; pre-dose, 1, 2,4, 8, 12 and 24 hrs post-dose on Day 14
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The pharmacokinetic parameters were calculated by standard non-compartmental analysis according to current working practices and using WinNonlin Version 5.2 or higher.
All calculations of non-compartmental parameters were based on actual sampling times.
AUC (0-inf) could not be determined as data was below the limit of quantification.
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Pre-dose and 2 hrs on Day 1 and 7; pre-dose, 1, 2,4, 8, 12 and 24 hrs post-dose on Day 14
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Area Under the Concentration-time Curve From Time Zero (Pre-dose) to Last Time of Quantifiable Concentration Within a Participant Across All Treatments [AUC(0-t)] of GSK1278863 (Part A)
Tijdsspanne: Pre-dose and 0.25, 0.5, 1, 2, 4, 8, 12, 24, 48 and 72 hrs post-dose
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The pharmacokinetic parameters were calculated by standard non-compartmental analysis according to current working practices and using WinNonlin Version 5.2 or higher.
All calculations of non-compartmental parameters were based on actual sampling times.
AUC (0-t) could not be determined as data was below the limit of quantification.
|
Pre-dose and 0.25, 0.5, 1, 2, 4, 8, 12, 24, 48 and 72 hrs post-dose
|
|
AUC(0-t) of GSK1278863 (Part B)
Tijdsspanne: Pre-dose and 2 hrs on Day 1 and 7; pre-dose, 1, 2,4, 8, 12 and 24 hrs post-dose on Day 14
|
The pharmacokinetic parameters were calculated by standard non-compartmental analysis according to current working practices and using WinNonlin Version 5.2 or higher.
All calculations of non-compartmental parameters were based on actual sampling times.
AUC (0-t) could not be determined as data was below the limit of quantification.
|
Pre-dose and 2 hrs on Day 1 and 7; pre-dose, 1, 2,4, 8, 12 and 24 hrs post-dose on Day 14
|
Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Sponsor
Publicaties en nuttige links
De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start (Werkelijk)
17 juni 2013
Primaire voltooiing (Werkelijk)
10 februari 2017
Studie voltooiing (Werkelijk)
10 februari 2017
Studieregistratiedata
Eerst ingediend
11 april 2013
Eerst ingediend dat voldeed aan de QC-criteria
11 april 2013
Eerst geplaatst (Schatting)
15 april 2013
Updates van studierecords
Laatste update geplaatst (Werkelijk)
19 augustus 2019
Laatste update ingediend die voldeed aan QC-criteria
28 juni 2019
Laatst geverifieerd
1 juni 2019
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- 115760
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Ja
Beschrijving IPD-plan
IPD for this study will be made available via the Clinical Study Data Request site.
IPD-tijdsbestek voor delen
IPD is available via the Clinical Study Data Request site (click on the link provided below)
IPD-toegangscriteria voor delen
Access is provided after a research proposal is submitted and has received approval from the Independent Review Panel and after a Data Sharing Agreement is in place.
Access is provided for an initial period of 12 months but an extension can be granted, when justified, for up to another 12 months.
IPD delen Ondersteunend informatietype
- Leerprotocool
- Statistisch Analyse Plan (SAP)
- Formulier voor geïnformeerde toestemming (ICF)
- Klinisch onderzoeksrapport (CSR)
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .