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"}}},"trialDetailsJson":{"title":"Details Page","returnSearch":"Back to search results","description":"Study Description","identifier":"ViiV Study ID","clinicalID":"Clinicaltrials.gov Identifier","EudraCtID":"EudraCT Number","resultsAvailable":"Has Results Available Below","docAvailable":"Has Results Document Available","studyOverview":"Study Overview","overviewSection":{"conditionsDisplay":"Medical Conditions","product":"Product","collaborators":"Collaborators","dates":"Date","studyType":"Type","phase":"Phase","gender":"Gender","age":"Age","acceptVolunteers":"Accepts Healthy Volunteers"},"studyDocuments":"Study Documents","noDocuments":"No documents available","studyDocumentsAdditionalText":"If you wish to request for Full Study Report, please contact - ","studyDocumentsAdditionalEmail":"GSKClinicalSupportHD@gsk.com","isReleased":{"firstPart":"This study has Protocol and Result summary on ClinicalTrial.gov. Click","secondPart":"to learn more.","linkText":"here"},"mapLocations":"Locations","centralContact":"Central Contact","centralPhone":"Central Contact Phone","centralEmail":"Central Contact Email","mapSection":{"site":"GSK Investigational Site","condition":"Condition","id":"Study ID","city":"City","state":"State","zip":"Zip","country":"Country"},"studyDesign":"Study Design","designSection":{"purpose":"Primary Purpose","allocation":"Allocation","study_design":"Study Design","study_classification":"Study Classification","masking":"Masking","masked_subject":"Masked Subject","masked_caregiver":"Masked Caregiver","masked_investigator":"Masked Investigator","masked_assessor":"Masked Assessor","primary_outcomes":"Primary Outcomes","secondary_outcomes":"Secondary Outcomes","arms":"Arms","interventions":"Interventions","keyword":"Keyword","inclusionTitle":"Inclusion Criteria","exclusionTitle":"Exclusion Criteria","criteriaText":"Inclusion/Exclusion Criteria","criteria_button":"Click to view inclusion/exclusion criteria","enrollment":"Enrollment","clinicalPublications":"Clinical Publications"},"popoversText":{"studyId":{"childMarkdownRemark":{"html":"A unique number for a study given by ViiV.
"}},"ctGov":{"childMarkdownRemark":{"html":"This number identifies the study on the US clinicaltrials.gov register. Click this link to go to the entry for this study on Clinicaltrials.gov where you will be able to see protocol and results summaries where available.
"}},"eudraCT":{"childMarkdownRemark":{"html":"This number identifies the study on the EU clinicaltrials.eu register. Click this link to go to the entry for this study on clinicaltrials.eu where you will be able to see protocol and results summaries where available.
"}}}},"site":{"siteMetadata":{"siteUrl":"https://www.viiv-studyregister.com"}},"studyDetails":{"nct_number":"NCT03149848","ctis_id":"","HasResults":"false","IpdAccessCriteria":"","IpdDescription":"","IpdInfoTypeAnalyticCode":"","IpdInfoTypeIcf":"","IpdInfoTypeCsr":"","IpdInfoTypeProtocol":"","IpdInfoTypeSap":"","IpdTimeFrame":"","IpdUrl":"http://","IsFlexibleTrial":false,"IsReleasedToCtGov":"true","MaskingInfo":{"masked_assessor":"false","masked_caregiver":"false","masked_investigator":"false","masked_subject":"false","masking_description":"","no_masking":"true"},"PatientLevelData":"false","SharingIpd":"None","acronym":"","allocation":"Randomized","arm_groups":[{"arm_group_label":"Treatment A","arm_group_description":"Participants will be administered a single oral dose of CAB 30 mg after an overnight fast of at least 6 hours for 14 days in Period 1. Dosing of study medication on non-PK days may be with or without food.","arm_type":"Experimental"},{"arm_group_label":"Treatment B","arm_group_description":"Participants will be administered a single dose of RBT 300 mg and a single dose of CAB 30 mg after an overnight fast of at least 6 hours once daily for 14 days in Period 2. Dosing of study medication on non-PK days may be with or without food.","arm_type":"Experimental"}],"assignment":"Crossover Assignment","brief_summary":"This is a Phase I, single-center, open-label, fixed-sequence, 2-period crossover study in healthy adults to evaluate the effect of oral rifabutin (RBT) 300 milligram (mg) on the pharmacokinetics of oral cabotegravir (CAB) 30 milligram ( mg). This study will evaluate the drug-drug interaction (DDI) potential between CAB and RBT to inform dosing strategies for tuberculosis in subjects receiving CAB for human immunodeficiency virus (HIV) treatment or prevention. In Treatment Period 1 (Treatment A) participants will receive CAB 30 mg once daily for 14 days, followed by Treatment Period 2 (Treatment B) where participants will receive RBT 300 mg once daily with CAB 30 mg once daily for 14 days. The total study duration will be approximately for 10 weeks. Approximately 15 healthy subjects will be enrolled to ensure that 12 subjects complete dosing and critical assessments.","brief_summary_OneLinkTx":"","brief_title_OneLinkTx":"","brief_title":"Effect of rifabutin on the pharmacokinetics of oral cabotegravir in healthy subjects","conditions":[{"DisplayValue":"Human Immunodeficiency Virus (HIV)","DisplayValue_OneLinkTx":"","InternalValue":"CON_HIV","LookupValue":"Infection, Human Immunodeficiency Virus","LookupValue_OneLinkTx":""}],"created_date":"09/15/2018 17:21:22","criteria":"Inclusion Criteria - Males and females between 18 and 65 years of age inclusive, at the time of signing the informed consent. - Healthy as determined by the investigator or medically qualified designee based on a medical evaluation including medical history, physical examination, laboratory tests and cardiac monitoring. - A subject with a clinical abnormality or laboratory parameter(s) which is/are not specifically listed in the inclusion or exclusion criteria, outside the reference range for the population being studied may be included only if the investigator in consultation with the Medical Monitor agree and document that the finding is unlikely to introduce additional risk factors and will not interfere with the study procedures. Additionally, laboratory assessments that are specifically listed in the inclusion or exclusion criteria and are outside of the reference range can be repeated once during the screening period. - Body weight >=50 kilogram (kg) and body mass index (BMI) within the range 18.5 – 31.0 kg/ meter square (kg/m^2) (inclusive). - A female subject is eligible to participate if she is not pregnant (as confirmed by a negative serum human chorionic gonadotrophin (hCG) test), not lactating, and if she is of: • Non-reproductive potential defined as pre-menopausal with documented tubal ligation, hysteroscopic tubal occlusion procedure with follow-up confirmation of bilateral tubal occlusion, Hysterectomy, Bilateral Oophorectomy, Postmenopausal defined as 12 months of spontaneous amenorrhea [in questionable cases a blood sample with simultaneous follicle stimulating hormone (FSH) and estradiol levels consistent with menopause FSH: >40 milli international unit/mililiter (MIU/mL) and estradiol <40 picogram (pg)/mL (<147 picomoles/L) is confirmatory]; • Reproductive potential and agrees to follow one of the options listed in the Modified List of Highly Effective Methods for Avoiding Pregnancy in Females of Reproductive Potential (FRP) from 30 days prior to the first dose of study medication until the completion of the follow-up visit. The investigator is responsible for ensuring that subjects understand how to properly use these methods of contraception. - Capable of giving signed informed consent which includes compliance with the requirements and restrictions listed in the consent form and in this protocol. - ALT, alkaline phosphatase and bilirubin <=1x upper limit of normal (ULN) (isolated bilirubin >1.5xULN is acceptable if bilirubin is fractionated and direct bilirubin <35%). - White blood cell count and absolute neutrophil count in the normal range. Exclusion Criteria - 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 clinically significant cardiovascular disease including • Exclusion criteria for screening ECG (a single repeat is allowed for eligibility determination): male subjects with heart rate <45 and >100 beats per minute (bpm) and female subjects with heart rate <50 and >100 bpm, QRS duration (males and females) >120 millisecond (msec), QTc corrected by Fridericia's formula (QTcF) >450 msec for males and females. • Evidence of previous myocardial infarction (pathologic Q waves, S-T segment changes (except early repolarization). • 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. • Conduction abnormality (including but not specific to left or right complete bundle branch block, AV block [2nd degree (type II) or higher], Wolf Parkinson White [WPW] syndrome) which in the opinion of the principal Investigator and Viiv Medical Monitor, will interfere with the safety for the individual subject. • Sinus pauses >3 seconds. • Any significant arrhythmia which, in the opinion of the principal Investigator and ViiV Medical Monitor, will interfere with the safety for the individual subject. • Non-sustained (>=3 consecutive ventricular ectopic beats) or sustained ventricular tachycardia. - History of inflammatory bowel disease. - History of cholecystectomy or other gastrointestinal surgery (except appendectomy more than three months prior to study). - History of peptic ulceration or pancreatitis within the preceding 6 months of screening. - Participants determined by the Investigator to have a high risk of seizures, including participants with an unstable or poorly controlled seizure disorder. A participant with a prior history of seizure may be considered for enrolment if the Investigator believes the risk of seizure recurrence is low. All cases of prior seizure history should be discussed with the Medical Monitor prior to enrolment. - Current or past history of uveitis. - Any other medical condition which, in the judgment of the investigator and medical monitor, could jeopardize the safety of the subject or the integrity of the data derived from that subject. This includes but is not limited to any pre-existing condition that interferes with normal gastrointestinal anatomy or motility that could interfere with the absorption, metabolism, and/or excretion of the study drug. - 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 ViiV Medical Monitor the medication will not interfere with the study procedures or compromise subject safety. - History of regular alcohol consumption within 6 months of the study defined as an average weekly intake of >14 drinks. One drink is equivalent to 12 gram of alcohol, 12 ounces (360 mL) of beer, 5 ounces (150 mL) of wine or 1.5 ounces (45 mL) of 80 proof distilled spirits. - A history of regular use of tobacco, or nicotine-containing products within 30 days prior to screening. - 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 Medical Monitor, contraindicates their participation. - Presence of Hepatitis B surface antigen (HBsAg) positivity at screening or within 3 months prior to first dose of study treatment. Positive Hepatitis B core antibody (HBcAb) with negative hepatitis B surface antibody should also be excluded. - Positive Hepatitis C antibody test. - A positive pre-study drug/alcohol screen. - A positive test for HIV antibody. - A positive QuantiFERON Gold test or clinical evidence of tuberculosis (TB) infection. - Where participation in the study would result in donation of blood or blood products in excess of 500 mL within a 56 day period. - 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.","detailed_description":"","display_gender":"Both","display_gender_internal":"GENDER_ALL","display_phase":"Phase 1","display_phase_internal":"PHASE_1","display_status":"Completed","display_status_internal":"RECSTATUS_I_COMPLETED","endpoint":"","enrollment":"15","exclusion":"","gender":"All","gender_based":"No","gender_description":"","healthy_volunteers":"Yes","id":"343b0958-6db1-5761-9ba6-16ca9bebce47","internal":{"content":null,"contentDigest":"68f7af203729acbc4e23a9d8de9d357d","description":null,"fieldOwners":null,"mediaType":null,"ignoreType":null,"owner":"default-site-plugin","type":"studyDetails"},"inclusion":"Inclusion Criteria - Males and females between 18 and 65 years of age inclusive, at the time of signing the informed consent. - Healthy as determined by the investigator or medically qualified designee based on a medical evaluation including medical history, physical examination, laboratory tests and cardiac monitoring. - A subject with a clinical abnormality or laboratory parameter(s) which is/are not specifically listed in the inclusion or exclusion criteria, outside the reference range for the population being studied may be included only if the investigator in consultation with the Medical Monitor agree and document that the finding is unlikely to introduce additional risk factors and will not interfere with the study procedures. Additionally, laboratory assessments that are specifically listed in the inclusion or exclusion criteria and are outside of the reference range can be repeated once during the screening period. - Body weight >=50 kilogram (kg) and body mass index (BMI) within the range 18.5 – 31.0 kg/ meter square (kg/m^2) (inclusive). - A female subject is eligible to participate if she is not pregnant (as confirmed by a negative serum human chorionic gonadotrophin (hCG) test), not lactating, and if she is of: • Non-reproductive potential defined as pre-menopausal with documented tubal ligation, hysteroscopic tubal occlusion procedure with follow-up confirmation of bilateral tubal occlusion, Hysterectomy, Bilateral Oophorectomy, Postmenopausal defined as 12 months of spontaneous amenorrhea [in questionable cases a blood sample with simultaneous follicle stimulating hormone (FSH) and estradiol levels consistent with menopause FSH: >40 milli international unit/mililiter (MIU/mL) and estradiol <40 picogram (pg)/mL (<147 picomoles/L) is confirmatory]; • Reproductive potential and agrees to follow one of the options listed in the Modified List of Highly Effective Methods for Avoiding Pregnancy in Females of Reproductive Potential (FRP) from 30 days prior to the first dose of study medication until the completion of the follow-up visit. The investigator is responsible for ensuring that subjects understand how to properly use these methods of contraception. - Capable of giving signed informed consent which includes compliance with the requirements and restrictions listed in the consent form and in this protocol. - ALT, alkaline phosphatase and bilirubin <=1x upper limit of normal (ULN) (isolated bilirubin >1.5xULN is acceptable if bilirubin is fractionated and direct bilirubin <35%). - White blood cell count and absolute neutrophil count in the normal range. Exclusion Criteria - 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 clinically significant cardiovascular disease including • Exclusion criteria for screening ECG (a single repeat is allowed for eligibility determination): male subjects with heart rate <45 and >100 beats per minute (bpm) and female subjects with heart rate <50 and >100 bpm, QRS duration (males and females) >120 millisecond (msec), QTc corrected by Fridericia's formula (QTcF) >450 msec for males and females. • Evidence of previous myocardial infarction (pathologic Q waves, S-T segment changes (except early repolarization). • 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. • Conduction abnormality (including but not specific to left or right complete bundle branch block, AV block [2nd degree (type II) or higher], Wolf Parkinson White [WPW] syndrome) which in the opinion of the principal Investigator and Viiv Medical Monitor, will interfere with the safety for the individual subject. • Sinus pauses >3 seconds. • Any significant arrhythmia which, in the opinion of the principal Investigator and ViiV Medical Monitor, will interfere with the safety for the individual subject. • Non-sustained (>=3 consecutive ventricular ectopic beats) or sustained ventricular tachycardia. - History of inflammatory bowel disease. - History of cholecystectomy or other gastrointestinal surgery (except appendectomy more than three months prior to study). - History of peptic ulceration or pancreatitis within the preceding 6 months of screening. - Participants determined by the Investigator to have a high risk of seizures, including participants with an unstable or poorly controlled seizure disorder. A participant with a prior history of seizure may be considered for enrolment if the Investigator believes the risk of seizure recurrence is low. All cases of prior seizure history should be discussed with the Medical Monitor prior to enrolment. - Current or past history of uveitis. - Any other medical condition which, in the judgment of the investigator and medical monitor, could jeopardize the safety of the subject or the integrity of the data derived from that subject. This includes but is not limited to any pre-existing condition that interferes with normal gastrointestinal anatomy or motility that could interfere with the absorption, metabolism, and/or excretion of the study drug. - 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 ViiV Medical Monitor the medication will not interfere with the study procedures or compromise subject safety. - History of regular alcohol consumption within 6 months of the study defined as an average weekly intake of >14 drinks. One drink is equivalent to 12 gram of alcohol, 12 ounces (360 mL) of beer, 5 ounces (150 mL) of wine or 1.5 ounces (45 mL) of 80 proof distilled spirits. - A history of regular use of tobacco, or nicotine-containing products within 30 days prior to screening. - 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 Medical Monitor, contraindicates their participation. - Presence of Hepatitis B surface antigen (HBsAg) positivity at screening or within 3 months prior to first dose of study treatment. Positive Hepatitis B core antibody (HBcAb) with negative hepatitis B surface antibody should also be excluded. - Positive Hepatitis C antibody test. - A positive pre-study drug/alcohol screen. - A positive test for HIV antibody. - A positive QuantiFERON Gold test or clinical evidence of tuberculosis (TB) infection. - Where participation in the study would result in donation of blood or blood products in excess of 500 mL within a 56 day period. - 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.","interventions":[{"arm_group_label":"Treatment B","intervention_description":"It will be available as a white aquarius film coated tablet for oral administration. CAB Tablet is composed of GSK1265744B (micronized) lactose monohydrate, microcrystalline cellulose, hypromellose, sodium starch glycolate, magnesium stearate","intervention_name":"Cabotegravir","intervention_type":"Drug"},{"arm_group_label":"Treatment A","intervention_description":"It will be available as a white aquarius film coated tablet for oral administration. CAB Tablet is composed of GSK1265744B (micronized) lactose monohydrate, microcrystalline cellulose, hypromellose, sodium starch glycolate, magnesium stearate","intervention_name":"Cabotegravir","intervention_type":"Drug"},{"arm_group_label":"Treatment B","intervention_description":"It will be available as an opaque red-brown hard gelatin capsules containing 150 mg of rifabutin for oral administration. These capsules are composed of rifabutin, microcrystalline cellulose, sodium lauryl sulphate, magnesium stearate, and silica gel","intervention_name":"Rifabutin","intervention_type":"Drug"}],"interventional_subtype":"Treatment","is_fda_regulated":false,"is_high_value":false,"is_ind_study":false,"keywords":["Tuberculosis","Human Immunodeficiency Virus","Rifabutin","Drug-drug interaction","Cabotegravir"],"last_follow_up_date":"09/06/2017 00:00:00","links":[],"locations":[{"City":"Cambridge","Latitude":"52.205337","CountryDisplay":"United Kingdom","Longitude":"0.121817","Name":"GSK Investigational Site","StateDisplay":null,"PostalCode":null,"StatusDisplay":"Completed","StatusDisplayInternal":"LOCSTATUS_COMPLETED","StatusMapped":"Study Complete"}],"masking":"","maximum_age_raw":"65 years","maximum_age":"65","minimum_age":"18","minimum_age_raw":"18 years","modified_date":"10/01/2018 22:40:31","number_of_arms":"2","observational_design":{"biospecimen_description":"","biospecimen_retention":"","number_of_groups":"","observational_study_design":"","patient_registry":"","target_duration_quantity":"","target_duration_units":"","timing":""},"official_title":"Phase I, single-center, open label, fixed-sequence cross-over study to evaluate the effect of rifabutin on the pharmacokinetics of oral cabotegravir in healthy subjects","org_study_id":"205712","overall_contact":{"email":"GSKClinicalSupportHD@gsk.com","last_name":"Call Center","phone":"877-379-3718"},"overall_status":"Completed - Interventional","oversight_info":{"exported_from_us":"","fda_regulated_device":"No","fda_regulated_drug":"No","ped_postmarket_surv":"","has_dmc":false,"post_prior_to_approval":"","regulatory_authorities":[""]},"phase":"1","primary_compl_date":"09/06/2017 00:00:00","primary_outcomes":[{"outcome_description":"Blood sample will be collected at indicated time points and concentration of CAB will be determined in plasma","outcome_measure":"Area under the concentration-time curve over one dosing interval AUC(0-tau) of CAB in Treatment Period 1 and 2","outcome_time_frame":"Period 1: Pre-dose on Day 13; and at pre-dose, 1, 2, 3, 4, 8, 12, and 24 hours (h) post –dose on Day 14. Period 2: Pre-dose on Day 26, 27 and day 28 and 1, 2, 3, 4, 8, 12, 24 h post-dose on Day 28.","outcome_safety_issue":null},{"outcome_description":"Blood sample will be collected at indicated time points and concentration of CAB will be determined in plasma","outcome_measure":"Maximum Observed Plasma Concentration (Cmax) of CAB in Treatment Period 1 and 2","outcome_time_frame":"Period 1: Pre-dose on Day 13; and at pre-dose, 1, 2, 3, 4, 8, 12, and 24 hours (h) post –dose on Day 14. Period 2: Pre-dose on Day 26, 27 and day 28 and 1, 2, 3, 4, 8, 12, 24 h post-dose on Day 28.","outcome_safety_issue":null}],"product_name":"","product_name_OneLinkTx":"","secondary_ids":[],"secondary_outcomes":[{"outcome_description":"Blood sample will be collected at indicated time points and concentration of CAB will be determined in plasma","outcome_measure":"Concentration of CAB at the end of the dosing interval (Ctau) in Treatment Period 1 and 2","outcome_time_frame":"Period 1: Pre-dose on Day 13; and at pre-dose, 1, 2, 3, 4, 8, 12, and 24 hours (h) post –dose on Day 14. Period 2: Pre-dose on Day 26, 27 and day 28 and 1, 2, 3, 4, 8, 12, 24 h post-dose on Day 28.","outcome_safety_issue":null},{"outcome_description":"Blood sample will be collected at indicated time points and concentration of CAB will be determined in plasma","outcome_measure":"Time to maximum observed plasma concentration (Tmax) of CAB in Treatment Period 1 and 2","outcome_time_frame":"Period 1: Pre-dose on Day 13; and at pre-dose, 1, 2, 3, 4, 8, 12, and 24 hours (h) post –dose on Day 14. Period 2: Pre-dose on Day 26, 27 and day 28 and 1, 2, 3, 4, 8, 12, 24 h post-dose on Day 28.","outcome_safety_issue":null},{"outcome_description":"Blood sample will be collected at indicated time points and concentration of CAB will be determined in plasma","outcome_measure":"Terminal phase half-life (t1/2) of CAB in Treatment Period 1 and 2","outcome_time_frame":"Period 1: Pre-dose on Day 13; and at pre-dose, 1, 2, 3, 4, 8, 12, and 24 hours (h) post –dose on Day 14. Period 2: Pre-dose on Day 26, 27 and day 28 and 1, 2, 3, 4, 8, 12, 24 h post-dose on Day 28.","outcome_safety_issue":null},{"outcome_description":"Blood sample will be collected at indicated time points and concentration of CAB will be determined in plasma","outcome_measure":"Apparent clearance of CAB following oral dosing (CL/F) in Treatment Period 1 and 2","outcome_time_frame":"Period 1: Pre-dose on Day 13; and at pre-dose, 1, 2, 3, 4, 8, 12, and 24 hours (h) post –dose on Day 14. Period 2: Pre-dose on Day 26, 27 and day 28 and 1, 2, 3, 4, 8, 12, 24 h post-dose on Day 28.","outcome_safety_issue":null},{"outcome_description":"An AE is any untoward medical occurrence in a clinical investigation subject, temporally associated with the use of a medicinal product, whether or not considered related to the medicinal product. Any untoward event resulting in death, life threatening, requires hospitalization or prolongation of existing hospitalization, results in disability/incapacity, congenital anomaly/birth defect or any other situation according to medical or scientific judgement will be categorized as SAE.","outcome_measure":"Number of subjects with adverse event (AE) and serious adverse event (SAE) in Treatment Period 1 and 2","outcome_time_frame":"Up to 10 weeks","outcome_safety_issue":null},{"outcome_description":"Concurrent medication will be assessed","outcome_measure":"Concurrent medication assessment","outcome_time_frame":"Up to 10 weeks","outcome_safety_issue":null},{"outcome_description":"Blood samples will be collected to analyze blood urea nitrogen (BUN), creatinine, glucose, total carbon dioxide, creatine phosphokinase (CPK), sodium, potassium, calcium, gamma-glutamyltransferase (GGT), aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (ALP), chloride, total and direct bilirubin, total protein and albumin","outcome_measure":"Number of subjects having abnormal clinical chemistry parameters as a measure of safety in Treatment Period 1 and 2","outcome_time_frame":"Up to 10 weeks","outcome_safety_issue":null},{"outcome_description":"Blood samples will be collected to analyze platelet counts, red blood cells (RBC) count, white blood cells (WBC) count (absolute), red cell distribution width (RDW), haemoglobin, hematocrit, RBC indices (mean corpuscular volume [MCV] and mean corpuscular haemoglobin [MCH]) and differential WBC count (neutrophils, lymphocytes, monocytes, eosinophils, and basophils).","outcome_measure":"Number of subjects having abnormal haematology parameters as a measure of safety in Treatment Period 1 and 2","outcome_time_frame":"Up to 10 weeks","outcome_safety_issue":null},{"outcome_description":"Urine samples will be collected to analyze specific gravity, determining pH, glucose, protein, blood and ketones by dipstick method, and microscopic examination (if blood or protein is abnormal).","outcome_measure":"Number of subjects having abnormal urinalysis as a measure of safety in Treatment Period 1 and 2","outcome_time_frame":"Up to 10 weeks","outcome_safety_issue":null},{"outcome_description":"12-lead ECGs will be obtained in a semi-supine position after 10 minutes of rest.","outcome_measure":"Electrocardiogram (ECG) assessment as a measure of safety in Treatment Period 1 and 2","outcome_time_frame":"Up to 10 weeks","outcome_safety_issue":null},{"outcome_description":"Systolic and diastolic blood pressure will be measured in semi-supine position after 10 minutes of rest","outcome_measure":"Systolic and diastolic blood pressure (BP) assessment as a safety measure in Treatment Period 1 and 2","outcome_time_frame":"Up to 10 weeks","outcome_safety_issue":null},{"outcome_description":"Heart rate will be measured in semi-supine position after 10 minutes of rest","outcome_measure":"Heart Rate (HR) assessment as a safety measure in Treatment Period 1 and 2","outcome_time_frame":"Up to 10 weeks","outcome_safety_issue":null},{"outcome_description":"Body temperature will be measured in semi-supine position after 10 minutes rest","outcome_measure":"Body temperature assessment as a safety measure in Treatment Period 1 and 2","outcome_time_frame":"Up to 10 weeks","outcome_safety_issue":null}],"sponsors":{"investigator_affiliation":"","investigator_username":"","lead_sponsor":"ViiV Healthcare","collaborators":["GlaxoSmithKline"]},"start_date":"06/06/2017 00:00:00","study_type":"Interventional","therapeutic_area":"Infectious Diseases","citations":[],"is_section_801":null}},"pageContext":{"studyId":"205712"}},"staticQueryHashes":["162689979","3332233851","3729204765","3769354840","399703114"]}