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This study met a protocol defined futility criterion and will be terminated following completion of the Follow Up Visit on the last subject randomised.
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This is an adaptive, dose ranging, Phase II study to investigate the relationship between repeat doses of GSK2586184 and the pharmacodynamic effect and clinical efficacy in patients with active systemic lupus erythematosus (SLE). This study will also investigate the safety and tolerability of repeat doses of GSK2586184. During the study, up to 3 Interim Analyses will be conducted. These are to monitor the pharmacodynamic effect and safety following 2 weeks of therapy (Interim Analysis 1); and the clinical efficacy and safety of GSK2586184 following 12 weeks of therapy (Interim Analyses 2 and 3). Subjects who meet the entry criteria (approximately 150 to 250) will be randomized in a 1:1:1:1:1 ratio to receive GSK2586184 at doses of 50 milligram (mg) twice daily (b.i.d), 100 mg b.i.d, 200 mg b.i.d, 400 mg b.i.d or Placebo b.i.d. GSK2586184 tablets available in 50 and 200 mg dose strength will be administered orally up to 12 weeks.
Subjects who complete the study will participate in the study for approximately 21 weeks.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| GSK2586184 50 mg Arm | Experimental | Subjects in the GSK2586184 50 mg Arm will receive twice daily dose of GSK2586184 50 mg 1 x 50 mg tablet + 1x placebo tablet) orally up to 12 weeks. Study medication should be taken with food, immediately following a meal |
|
| GSK2586184 100 mg Arm | Experimental | Subjects in the GSK2586184 100 mg Arm will receive twice daily dose of GSK2586184 100 mg (2 x 50 mg tablets) orally up to 12 weeks. Study medication should be taken with food, immediately following a meal. |
|
| GSK2586184 200 mg Arm | Experimental | Subjects in the GSK2586184 200 mg Arm will receive twice daily dose of GSK2586184 200 mg (1 x 200 mg tablet + 1x placebo tablet) orally up to 12 weeks. Study medication should be taken with food, immediately following a meal. |
|
| GSK2586184 400 mg Arm | Experimental | Subjects in the GSK2586184 400 mg Arm will receive twice daily dose of GSK2586184 400 mg (2 x 200 mg tablets) orally up to 12 weeks. Study medication should be taken with food, immediately following a meal. |
|
| Placebo | Placebo Comparator |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| GSK2586184 50 mg | Drug | GSK2586184 tablet will be administered orally as twice daily dose of 50 mg (1 x 50 mg tablet) up to 12 weeks. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Percentage Inhibition from Baseline of interferon (IFN) Transcriptional Biomarkers at Week 2 | Mean reduction (40%) from Baseline of the IFN transcriptional signature biomarker was monitored at Week 2. Percentage (Per) inhibition (=[(Day x-Baseline)/Baseline]*-100), was the Per reduction from Baseline (Day1) and evaluated in any pre-designated panels of genes i.e. Addenbrookes 1, Addenbrookes 2, JAK439, PD, Panel Stripping, Flare and Transcription. Analysis was performed using a repeated measures model with covariates of treatment, baseline, Day, Day by baseline and Day by treatment interactions. Only those Par available at the specified time points were analysed (n=X,X,X,X,X). Different Par may have been analysed at different time points, so the overall number of Par analysed reflects everyone in the Intent To Treat (ITT) Population i.e. Par randomised to treatment, received >=1 dose of study medication and had >=1 valid post dose assessment | Baseline(Day1) and Week 2 |
| Change from Baseline of SELENA SLEDAI score at indicated time points up to Week 16 | The Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) is a validated index for assessing SLE disease activity. It is a weighted index in which signs and symptoms, laboratory tests, and physician's assessment for each of 9 organ systems are given a weighted score and summed, if present at the time of the visit or in the preceding 10 days. Modified version of SLEDAI is Safety of Estrogen in Lupus National Assessment (SELENA) SLEDAI where the maximum theoretical score for the SELENA SLEDAI was 105 with 0 indicating inactive disease. Baseline value is defined as Day 1 (pre-dose) SELENA SLEDAI score. | Baseline(Day1), Weeks 2, 4, 6, 8, 10, 12 and 16 |
| Change from Baseline in systolic blood pressure and diastolic blood pressure at the indicated time points up to Week 16 | Change from Baseline in systolic blood pressure (BP) and diastolic BP is summarized for each post-Baseline assessment up to Week 16. Change from Baseline was calculated as the individual post-Baseline value minus the Baseline value. Baseline value is defined as the last Pre-treatment value observed. | Baseline(Day1), Weeks 2, 4, 6, 8, 10, 12 and 16 |
| Measure | Description | Time Frame |
|---|---|---|
| SRI Response Rate at Week 4, 8, 12 and 16 | The relationship between dose of GSK2586184 and clinical response was assessed by the SLE Responder Index (SRI). The percentage of participants achieving a response on the composite endpoint are summarized. Response is defined as:>= 4 point reduction from the Baseline in the SELENA SLEDAI score and no worsening (increase of <0.30 points from the Baseline) in Physicians Global Assessment (PGA),and no new British Isles Lupus Assessment Group (BILAG) A organ domain score or 2 new BILAG B organ domain scores compared with the Baseline. Baseline value is defined as the last Pre-treatment value observed. |
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Inclusion Criteria:
A female Subject is eligible to participate if she is not pregnant or nursing; is of non-childbearing potential. Females of child-bearing potential must agree to use one highly effective contraception method in addition to barrier protection OR two forms of highly effective contraception.
Exclusion Criteria:
Proteinuria > 0.5g/24 hour OR equivalent spot urine protein to creatinine ratio of 0.5mg/mg; Serum creatinine > 1.5 X upper limit of normal (ULN); active nephritis requiring acute therapy not permitted by protocol; required peritoneal dialysis or hemodialysis or high dose corticosteroid (> 100 mg/day prednisone or equivalent) within 90 days prior to first dose; active renal disease shown on renal biopsy in the three months prior to screening.
The subject has participated in a clinical trial and has received an investigational product within 30 days, 5 half-lives or twice the duration of the biological effect of the investigational product (whichever is longer) prior to the first dosing day in the current study; OR exposure to more than four new chemical entities within 12 months prior to the first dosing day.
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| Name | Affiliation | Role |
|---|---|---|
| GSK Clinical Trials | GlaxoSmithKline | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| GSK Investigational Site | Ciudad de Buenos Aires | Buenos Aires | C1431FWO | Argentina | ||
| GSK Investigational Site |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 27055521 | Derived | Kahl L, Patel J, Layton M, Binks M, Hicks K, Leon G, Hachulla E, Machado D, Staumont-Salle D, Dickson M, Condreay L, Schifano L, Zamuner S, van Vollenhoven RF; JAK115919 Study Team. Safety, tolerability, efficacy and pharmacodynamics of the selective JAK1 inhibitor GSK2586184 in patients with systemic lupus erythematosus. Lupus. 2016 Nov;25(13):1420-1430. doi: 10.1177/0961203316640910. Epub 2016 Jul 11. |
| Label | URL |
|---|---|
| Researchers can use this site to request access to anonymised patient level data and/or supporting documents from clinical studies to conduct further research. | View source |
| ID | Type | URL | Comment |
|---|---|---|---|
| 115919 | Individual Participant Data Set | View IPD |
Patient-level data for this study will be made available through www.clinicalstudydatarequest.com following the timelines and process described on this site.
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| Type | Date | Date Unknown |
|---|---|---|
| Release | Jul 19, 2017 | |
| Reset | Feb 16, 2018 |
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Subjects in the placebo arm will receive twice daily dose of 2 matching placebo tablets orally up to 12 weeks; taken with food, immediately following a meal. |
|
| GSK2586184 100 mg | Drug | GSK2586184 tablet will be administered orally as twice daily dose of (2 X 50 mg tablet) up to 12 weeks. |
|
| GSK2586184 200 mg | Drug | GSK2586184 tablet will be administered orally as twice daily dose of 200 mg (1 x 200 mg) up to 12 weeks. |
|
| GSK2586184 400 mg | Drug | GSK2586184 tablet will be administered orally as twice daily dose of (2 X 200 mg) up to 12 weeks. |
|
| Placebo | Drug | Matching placebo tablet will be administered orally twice daily up to 12 weeks. |
|
| Change from Baseline in heart rate at the indicated time points up to Week 16 | Change from Baseline in sitting and supine heart rate is summarized for each post-Baseline assessment up to Week 16. Change from Baseline was calculated as the individual post-Baseline value minus the Baseline value. Baseline value is defined as the last pre-treatment value observed. | Baseline (Day 1), Weeks 2, 4, 6, 8, 10, 12 and 16 |
| Change from Baseline in temperature at the indicated time points up to Week 16 | Change from Baseline in temperature is summarized for each post-Baseline assessment up to Week 16. Change from Baseline was calculated as the individual post-Baseline value minus the Baseline value. Baseline value is defined as the last Pre-treatment value observed. | Baseline (Day 1), Weeks 2, 4, 6, 8, 10, 12 and 16 |
| Change from Baseline in albumin, globulin and protein at the indicated time points up to Week 16 | Change from Baseline in the albumin, globulin and protein values are summarized for each post-Baseline assessment until Week 16. Change from Baseline was calculated as the individual post-Baseline value minus the Baseline value. Baseline value is defined as the last Pre-treatment value observed. | Baseline (Day 1), Weeks 2, 3, 4, 5, 6, 8, 10, 12 and 16 |
| Change from baseline in alkaline phosphatase, alanine amino transferase, aspartate amino transferase, creatine kinase, gamma glutamyl transferase and lactate dehydrogenase at the indicated time points up to Week 16 | Change from Baseline in the alkaline phosphatase (ALP), alanine amino transferase (ALT), aspartate amino transferase (AST), creatine kinase (CK), gamma glutamyl transferase (GGT) and lactate dehydrogenase (LDH) values are summarized for each post-Baseline assessment until Week 16. Change from Baseline was calculated as the individual post-Baseline value minus the Baseline value. Baseline value is defined as the last Pre-treatment value observed. | Baseline(Day 1), Weeks 2, 3, 4, 5, 6, 8, 10, 12 and 16 |
| Change from Baseline in anion gap, calcium, cholesterol, chloride, carbon dioxide, glucose, HDL cholesterol, potassium, LDL cholesterol, magnesium, phosphate, soidium, triglycerides, urea, VLDL cholesterol at the indicated time points up to Week 16 | Change from Baseline in the anion gap, calcium, ionised calcium, cholesterol, chloride, carbon dioxide, glucose, high density lipoprotein (HDL) cholesterol (fasted and not fasted), potassium, low density lipoprotein (LDL) cholesterol (fasted and not fasted), magnesium, phosphate, sodium, triglycerides (fasted and not fasted), urea and very low density lipoprotein (VLDL) cholesterol values are summarized for each post-Baseline assessment until Week 16. Change from Baseline was calculated as the individual post-Baseline value minus the Baseline value. Baseline value is defined as the last Pre-treatment value observed. | Baseline (Day 1), Weeks 2, 3, 4, 5, 6, 8, 10, 12 and 16 |
| Change from Baseline in bilirubin, creatinine, iron binding capacity, iron and urate at the indicated time points up to Week 16 | Change from Baseline in the bilirubin, direct and indirect bilirubin, creatinine, total iron binding capacity (TIBC), unsaturated iron binding capacity (UIBC), iron and uric acid values are summarized for each post-Baseline assessment until Week 16. Change from Baseline was calculated as the individual post-Baseline value minus the Baseline value. Baseline value is defined as the last Pre-treatment value observed. | Baseline(Day 1), Weeks 2, 3, 4, 5, 6, 8, 10, 12 and 16 |
| Change from Baseline in albumin/globulin, BUN/creatinine and transferrin saturation at the indicated time points up to Week 16 | Change from baseline in the albumin/globulin, blood urea nitrogen (BUN)/creatinine and transferrin saturation values are summarized for each post-Baseline assessment until Week 16. Change from Baseline was calculated as the individual post-Baseline value minus the Baseline value. Baseline value is defined as the last Pre-treatment value observed. | Baseline(Day 1), Weeks 2, 3, 4, 5, 6, 8, 10, 12 and 16 |
| Change from Baseline in creatinine clearance at the indicated time points up to Week 16 | Change from Baseline in the Creatinine Clearance values are summarized for each post-Baseline assessment until Week 16. Change from Baseline was calculated as the individual post-Baseline value minus the Baseline value. Baseline value is defined as the last Pre-treatment value observed. | Baseline (Day 1), Weeks 2, 3, 4, 5, 6, 8, 10, 12 and 16 |
| Change from Baseline in basophils, eosinophils, lymphocytes, monocytes, neutrophils, neutrophils segmented (SG), platelets and leukocytes at the indicated time points up to Week 16 | Change from Baseline in the basophils, eosinophils, lymphocytes, monocytes, neutrophils, neutrophils segmented (SG), platelets and leukocytes values are summarized for each post-Baseline assessment until Week 16. Change from Baseline was calculated as the individual post-Baseline value minus the Baseline value. Baseline value is defined as the last Pre-treatment value observed. | Baseline(Day 1), Weeks 1, 2, 3, 4, 5, 6, 8, 10, 12 and 16 |
| Change from Baseline in basophils/leukocytes, eosinophils/leukocytes, lymphocytes/leukocytes, monocytes/leukocytes, neutrophils/leukocytes, neutrophils SG/leukocytes and erythrocyte distribution width (EDW) at the indicated time points up to Week 16 | Change from Baseline in the basophils/leukocytes, eosinophils/leukocytes, lymphocytes/leukocytes, monocytes/leukocytes, neutrophils/leukocytes, neutrophils segmented (SG)/leukocytes and erythrocyte distribution width (EDW) values are summarized for each post-Baseline assessment until Week 16. Change from Baseline was calculated as the individual post-Baseline value minus the Baseline value. Baseline value is defined as the last Pre-treatment value observed. | Baseline(Day 1), Weeks 1, 2, 3, 4, 5, 6, 8, 10, 12 and 16 |
| Change from Baseline in erythrocytes and reticulocytes at the indicated time points up to Week 16 | Change from Baseline in the erythrocyte and reticulocyte values are summarized for each post-Baseline assessment until Week 16. Change from Baseline was calculated as the individual post-Baseline value minus the Baseline value. Baseline value is defined as the last Pre-treatment value observed. | Baseline (Day 1), Weeks 1, 2, 3, 4, 5, 6, 8, 10, 12 and 16 |
| Change from Baseline in hemoglobin and erythrocyte mean corpuscular hemoglobin concentration (EMCHC) at the indicated time points up to Week 16 | Change from Baseline in the hemoglobin and erythrocyte mean corpuscular hemoglobin concentration (EMCHC) values are summarized for each post-Baseline assessment until Week 16. Change from Baseline was calculated as the individual post-Baseline value minus the Baseline value. Baseline value is defined as the last Pre-treatment value observed. | Baseline(Day 1), Weeks 1, 2, 3, 4, 5, 6, 8, 10, 12 and 16 |
| Change from Baseline in erythrocyte mean corpuscular hemoglobin (EMCH) at the indicated time points up to Week 16 | Change from Baseline in the hemoglobin and erythrocyte mean corpuscular hemoglobin (EMCH) values are summarized for each post-Baseline assessment until Week 16. Change from Baseline was calculated as the individual post-Baseline value minus the Baseline value. Baseline value is defined as the last Pre-treatment value observed. | Baseline(Day 1), Weeks 1, 2, 3, 4, 5, 6, 8, 10, 12 and 16 |
| Change from Baseline in erythrocyte mean corpuscular volume (EMCV) and mean platelet volume (MPV) at the indicated time points up to Week 16 | Change from Baseline in the erythrocyte mean corpuscular volume (EMCV) and mean platelet volume (MPV) values are summarized for each post-Baseline assessment until Week 16. Change from Baseline was calculated as the individual post-Baseline value minus the Baseline value. Baseline value is defined as the last Pre-treatment value observed. | Baseline(Day 1), Weeks 1, 2, 3, 4, 5, 6, 8, 10, 12 and 16 |
| Change from Baseline in hematocrit and reticulocytes/erythrocytes at the indicated time points up to Week 16 | Change from Baseline in the hematocrit and reticulocytes/erythrocytes values are summarized for each post-Baseline assessment until Week 16. Change from Baseline was calculated as the individual post-Baseline value minus the Baseline value. Baseline value is defined as the last Pre-treatment value observed. | Baseline(Day 1), Weeks 1, 2, 3, 4, 5, 6, 8, 10, 12 and 16 |
| Number of participants with urinalysis data at the indicated time points up to Week 16 | Number of participants with negative and positives (trace, +, ++ and +++) data for urine glucose (UGLU), urine ketones (UKET) and urine occult blood (UOB) are summarized for each post-Baseline assessment until Week 16. Urinalysis was performed by dipstick method. Baseline value is defined as the last Pre-treatment value observed. | Baseline(Day 1), Weeks 1, 2, 3, 4, 5, 6, 8, 10, 12 and 16 |
| Change from Baseline in urine protein at the indicated time points up to Week 16 | Change from Baseline in the urine protein values are summarized for each post-Baseline assessment until Week 16. Change from Baseline was calculated as the individual post-Baseline value minus the Baseline value. Baseline value is defined as the last Pre-treatment value observed. | Baseline(Day 1), Weeks 2, 3, 4, 5, 6, 8, 10, 12 and 16 |
| Change from Baseline in urine protein/creatinine at the indicated time points up to Week 16 | Change from Baseline in the urine protein/creatinine values are summarized for each post-Baseline assessment until Week 16. Change from Baseline was calculated as the individual post-Baseline value minus the Baseline value. Baseline value is defined as the last Pre-treatment value observed. | Baseline(Day 1), Weeks 2, 3, 4, 5, 6, 8, 10, 12 and 16 |
| Number of participants with any adverse events (AEs) and any serious adverse events (SAEs) up to Week 16 | An AE is defined as any untoward medical occurrence in a participant temporally associated with the use of a medicinal product, whether or not considered related to the medicinal product. An AE can therefore be any unfavorable and unintended sign(including an abnormal laboratory finding), symptom, or disease(new or exacerbated) temporally associated with the use of a medicinal product. An SAE is defined as 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, a congenital anomaly/birth defect, important medical events that jeopardize the participants or may require medical or surgical intervention to prevent one of the other outcomes listed in the above definition. | Up to Week 16 |
| Number of participants with severity Grade 1, 2, 3, 4 and 5 adverse events (AEs) | The Common Terminology Criteria for Adverse Events (CTCAE, Version 4) has categorised AEs in five grades. Grade refers to the severity of the AE. Grade 1: Mild; asymptomatic or mild symptoms; clinical or diagnostic observations only; intervention not indicated. Grade 2: Moderate; minimal, local or non-invasive intervention indicated; limiting age-appropriate instrumental activities of daily living. Grade 3: Severe or medically significant but not immediately life-threatening; hospitalization or prolongation of hospitalization indicated; disabling; limiting self care activities of daily living. Grade 4: Life-threatening consequences; urgent intervention indicated. Grade 5: Death related to AE. | Up to 16 Weeks |
| Week 4, 8, 12 and 16 |
| Change from baseline in SLEDAI-2K score and the S2K RI-50 score over time (up to Week 12) | The relationship between dose of GSK2586184 and clinical response was assessed by Systemic Lupus Erythematosus Disease Activity Index 2000 (SLEDAI-2K) and SLEDAI-2K Responder Index 50 (S2K RI-50) scores. SLEDAI-2K is a revised version of the SLEDAI in which the persistent active disease in the items rash, alopecia, mucosal ulcers and proteinuria would be scored as opposed to new occurrences as are measured in the SLEDAI. S2K RI-50 detects a minimum 50% improvement in disease manifestations among lupus participants. It covers 9 organ systems, utilising the same 24 descriptors and reflects disease activity over the previous 30 days. Change from Baseline was calculated as the individual post-Baseline value minus the Baseline value. Baseline value is defined as the last Pre-treatment value observed. Due to early termination of the study, data for this endpoint was not summarized. | Baseline(Day 1) to Week 12 |
| Mean GSK2586184 plasma concentrations on Weeks 2, 4, 6, 8, 10 and 12 | Plasma pharmacokinetic (PK) pre-dose (PRD) samples were collected for all participants at Weeks 2, 4, 8, 10 and 12 prior to the morning dose. At Week 2, additional blood sample were collected at 1hour (hr) and 4 hr post-dose (POD) and at Week 6, additional blood sample were collected, from 6 hr to 10 hr POD. PK Population comprised of all participants randomised to treatment, who have taken at least one dose. Only participants for whom plasma PK samples were obtained were assessed (represented by n=X,X,X,X in category titles). Different participants may have been analysed at different time points, so the overall number of participants analysed reflects everyone in the Pharmacokinetic(PK) Population. | Weeks 2, 4, 6, 8, 10 and 12 |
| Area under the concentration-time curve over the dosing interval (AUC[0-tau]) up to Week 12 | Plasma PK PRD samples were collected for all participants at Weeks 2, 4, 8, 10 and 12 prior to the morning dose. At Week 2, additional blood sample were collected at 1hr and 4 hr POD and at Week 6, additional blood sample were collected, from 6 hr to 10 hr POD. AUC(0-tau).is calculated from a population pharmacokinetic model using Non Linear Mixed Effect Model (NONMEM) after log-transformation of PK data. Only participants for whom plasma PK samples were obtained and assessed. | Weeks 2, 4, 6, 8, 10 and 12 |
| Apparent clearance (CL/F) up to Week 12 | Plasma PK PRD samples were collected for all participants at Weeks 2, 4, 8, 10 and 12 prior to the morning dose. At Week 2, additional blood sample were collected at 1hr and 4 hr POD and at Week 6, additional blood sample were collected, from 6 hr to 10 hr POD. CL/F is calculated, as dose divided by AUC(0-tau), from a population pharmacokinetic model using Non Linear Mixed Effect Model (NONMEM) after log-transformation of PK data. Only participants for whom plasma PK samples were obtained and assessed. | Weeks 2, 4, 6, 8, 10 and 12 |
| Volume of distribution (Vss) up to Week 12 | Plasma PK PRD samples were collected for all participants at Weeks 2, 4, 8, 10 and 12 prior to the morning dose. At Week 2, additional blood sample were collected at 1hr and 4 hr POD and at Week 6, additional blood sample were collected, from 6 hr to 10 hr POD. Apparent volume of distribution is calculated as dose divided by (AUC[0-tau] lambda z) where lambda z is the terminal phase rate constant. Vss is calculated from a population pharmacokinetic model using Non Linear Mixed Effect Model (NONMEM) after log-transformation of PK data. Only participants for whom plasma PK samples were obtained and assessed | Weeks 2, 4, 6, 8, 10 and 12 |
| Mean change from Baseline in the SF-36 Domain Scores up to Week 16 | The Short Form (36) Health Survey (SF-36v2 ) is a participant-reported survey of participant health and measures general health-related quality of life. There are 36 items grouped into nine health domains: Physical Functioning, Role Physical, Bodily Pain, General Health, Vitality, Social Functioning, Role Emotional, Mental Health, Reported health transition (RHT). SF-36v2 gives a score for each of these domains based on the questions as assessed by participants. The lower the score the more disability and the higher the score the less disability. Change from Baseline was calculated as the individual post-Baseline value minus the Baseline value. Baseline value is defined as the last Pre-treatment value observed. | Baseline(Day 1), Weeks 12 and 16 |
| Mean change from Baseline in the Brief Fatigue Inventory (BFI) Domain Score up to Week 16 | The BFI was developed to quickly measure severity of fatigue in participants as well as its impact on their ability to function over the previous 24 hrs. It consists of nine items that look at fatigue in the past that are rated on a 0 -10 numeric rating scale where 0 is no fatigue or does not interfere and 10 is bad fatigue or completely interferes with activity. Change from Baseline was calculated as the individual post-Baseline value minus the Baseline value. Baseline value is defined as the last Pre-treatment value observed. | Baseline (Day 1), Weeks 2, 4, 6, 8, 10, 12 and 16 |
| Mean change from Baseline in the Brief Pain Inventory (BPI) Domain Score up to Week 16 | The BPI is a questionnaire used to assess the severity of pain and the impact of pain on daily functioning in the following areas: general activity, mood, walking ability, normal work, including outside the home and housework, relations with other people, enjoyment of life and sleep. Two sub scores are derived from questionnaire: the worst pain score and the interference score. To derive a valid worst pain score, a minimum of 3 (out of 6) non missing values were required versus 4 (out of 7) for the interference score. Change from Baseline was calculated as the individual post-Baseline value minus the Baseline value. Baseline value is defined as the last Pre-treatment value observed. | Baseline(Day 1), Weeks 2, 4, 6, 8, 10, 12 and 16 |
| Rosario |
| Santa Fe Province |
| 2000 |
| Argentina |
| GSK Investigational Site | San Juan | J5402DIL | Argentina |
| GSK Investigational Site | Santiago | Región Metro de Santiago | Chile |
| GSK Investigational Site | Olomouc | 775 20 | Czechia |
| GSK Investigational Site | Prague | 12850 | Czechia |
| GSK Investigational Site | Tallinn | 11312 | Estonia |
| GSK Investigational Site | Tallinn | 13419 | Estonia |
| GSK Investigational Site | Brest | 29609 | France |
| GSK Investigational Site | Lille | 59037 | France |
| GSK Investigational Site | Limoges | 87042 | France |
| GSK Investigational Site | Paris | 75651 | France |
| GSK Investigational Site | Pessac | 33604 | France |
| GSK Investigational Site | Cologne | North Rhine-Westphalia | 50937 | Germany |
| GSK Investigational Site | Herne | North Rhine-Westphalia | 44652 | Germany |
| GSK Investigational Site | Mainz | Rhineland-Palatinate | 55131 | Germany |
| GSK Investigational Site | Kiel | Schleswig-Holstein | 24105 | Germany |
| GSK Investigational Site | Jena | Thuringia | 07747 | Germany |
| GSK Investigational Site | Athens | 115 21 | Greece |
| GSK Investigational Site | Heraklion-Crete | 71110 | Greece |
| GSK Investigational Site | Larissa | 41110 | Greece |
| GSK Investigational Site | Thessaloniki | 546 42 | Greece |
| GSK Investigational Site | Hong Kong | Hong Kong |
| GSK Investigational Site | Shatin | Hong Kong |
| GSK Investigational Site | Tuenmen | Hong Kong |
| GSK Investigational Site | Budapest | 1023 | Hungary |
| GSK Investigational Site | Budapest | 1097 | Hungary |
| GSK Investigational Site | Debrecen | 4032 | Hungary |
| GSK Investigational Site | Zalaegerszeg | 8900 | Hungary |
| GSK Investigational Site | La Victoria | Lima region | Lima 13 | Peru |
| GSK Investigational Site | San Borja | Lima region | Peru |
| GSK Investigational Site | Surco | Lima region | Peru |
| GSK Investigational Site | Lima | Lima 27 | Peru |
| GSK Investigational Site | Bialystok | 15-297 | Poland |
| GSK Investigational Site | Gdynia | 81-384 | Poland |
| GSK Investigational Site | Lublin | 20-954 | Poland |
| GSK Investigational Site | Poznan | 60-856 | Poland |
| GSK Investigational Site | Poznan | 61-397 | Poland |
| GSK Investigational Site | Bucharest | 020125 | Romania |
| GSK Investigational Site | Bucharest | 11172 | Romania |
| GSK Investigational Site | Cluj-Napoca | 400006 | Romania |
| GSK Investigational Site | Cape Town | 7925 | South Africa |
| GSK Investigational Site | Parow | 7505 | South Africa |
| GSK Investigational Site | Pinelands, Cape Town | 7405 | South Africa |
| GSK Investigational Site | Stellenbosch | 7600 | South Africa |
| GSK Investigational Site | Seoul | 120-752 | South Korea |
| GSK Investigational Site | Seoul | 137-701 | South Korea |
| GSK Investigational Site | Seoul | 143-729 | South Korea |
| GSK Investigational Site | Madrid | 28046 | Spain |
| GSK Investigational Site | Santiago de Compostela | 15706 | Spain |
| GSK Investigational Site | Seville | 41013 | Spain |
| GSK Investigational Site | Gothenburg | SE-413 45 | Sweden |
| GSK Investigational Site | Linköping | SE-581 85 | Sweden |
For additional information about this study please refer to the GSK Clinical Study Register |
| 115919 | Informed Consent Form | View IPD | For additional information about this study please refer to the GSK Clinical Study Register |
| 115919 | Study Protocol | View IPD | For additional information about this study please refer to the GSK Clinical Study Register |
| 115919 | Dataset Specification | View IPD | For additional information about this study please refer to the GSK Clinical Study Register |
| 115919 | Annotated Case Report Form | View IPD | For additional information about this study please refer to the GSK Clinical Study Register |
| 115919 | Clinical Study Report | View IPD | For additional information about this study please refer to the GSK Clinical Study Register |
| 115919 | Statistical Analysis Plan | View IPD | For additional information about this study please refer to the GSK Clinical Study Register |
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| Release Date | Unrelease Date | Unrelease Date Unknown | Reset Date | MCP Release Number |
|---|---|---|---|---|
| Jul 19, 2017 | Feb 16, 2018 |
| ID | Term |
|---|---|
| D008180 | Lupus Erythematosus, Systemic |
| ID | Term |
|---|---|
| D003240 | Connective Tissue Diseases |
| D017437 | Skin and Connective Tissue Diseases |
| D001327 | Autoimmune Diseases |
| D007154 | Immune System Diseases |
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| ID | Term |
|---|---|
| C000604226 | GSK2586184 |
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