| Primary | Mean Change From Baseline in Six Minutes Walk Distance (6MWD) at Week 12 | Mean change from baseline was calculated as the Week 12 value minus the baseline value. 6MWD was measured by a 6 minute walk test. This test measures the distance that a subject can walk in a period of 6 minutes. | Full Analysis Set (FAS): all participants registered, with the exception of those who had not received any dose of the investigational product and those who had no efficacy assessment after administration of the investigational product. Imputation technique was last observation carried forward. | Posted | | Mean | Standard Deviation | Meters | | Baseline and Week 12 | | | | ID | Title | Description |
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| OG000 | GSK1325760A | GSK1325760A 5 mg once a day by Week 12. After Week 12, GSK1325760A 10 mg once a day (the dosage could be increased or decreased appropriately according to a participant's condition) |
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| | Group IDs | Group Description | Statistical Method | Statistical Comment | P-Value | P-Value Comment | Parameter Type | Parameter Value | Dispersion Type | Dispersion Value | Confidence Interval Sides | Confidence Interval % | CI Lower Limit | CI Upper Limit | CI Lower Limit Comment | CI Upper Limit Comment | Estimate Comment | Tested Non-Inferiority | Non-Inferiority Type | Non-Inferiority Comment | Other Analysis Description |
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| | | | | | Mean change | 33.49 | | | | 95 | 15.231 | 51.744 | | | | No | Superiority or Other | | |
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| Secondary | Mean Change From Baseline in Six Minutes Walk Distance (6MWD) at Week 24/Withdrawal | Change from baseline was calculated as the Week 24/Withdrawal value minus the basline value. 6MWD was measured by a 6 minute walk test. This test measures the distance that a subject can walk in a period of 6 minutes. Imputation technique was last observation carried forward. | | Posted | | Median | Standard Deviation | Meters | | Baseline and Week 24/Withdrawal | | | | ID | Title | Description |
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| OG000 | GSK1325760A | GSK1325760A 5 mg once a day by Week 12. After Week 12, GSK1325760A 10 mg once a day (the dosage could be increased or decreased appropriately according to a participant's condition) |
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| Secondary | Mean Change From Baseline in the Borg Dyspnea Index (BDI) at Weeks 12 and 24 | The BDI was calculated by using a 10-point scale (0 = None, 10 = Maximum). Change from baseline was calculated as the Week 12 and 24 values minus the baseline values. The BDI indicates the degree of breathlessness after completion of the 6 minute walk test. The BDI scale was assessed by each participant. Imputation technique was last observation carried forward. | | Posted | | Mean | Standard Deviation | Points on a scale | | Baseline and Weeks 12 and 24 | | | | ID | Title | Description |
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| OG000 | GSK1325760A | GSK1325760A 5 mg once a day by Week 12. After Week 12, GSK1325760A 10 mg once a day (the dosage could be increased or decreased appropriately according to a participant's condition) |
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| Secondary | Number of Participants With a Change From Baseline in Their World Health Organization (WHO) Functional Classification (FC) at Weeks 12 and 24 | There are four grades for WHO FC (class I = none, Class IV = most severe). The WHO FC indicates the severity of Pulmonary Arterial Hypertension and is an adaptation of the New York Heart Association classification. It was assessed by the investigator. Imputation technique was last observation carried forward. | | Posted | | Number | | Participants | | Weeks 12 and 24 | | | | ID | Title | Description |
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| OG000 | GSK1325760A | GSK1325760A 5 mg once a day by Week 12. After Week 12, GSK1325760A 10 mg once a day (the dosage could be increased or decreased appropriately according to a participant's condition) |
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| Secondary | Number of Participants With the Indicated Event, as an Assessment of Time to Clinical Worsening of Pulmonary Arterial Hypertension (PAH) at Week 24, Assessed as the First Occurrence of a Particular Event | Time to clinical worsening is defined as the time from baseline to the first occurrence of death, lung transplantation, hospitalization for PAH treatment, atrial septostomy, or study discontinuation due to change to other PAH treatment. Time to clinical worsening is measured as the number of participants who experienced these events during 24 weeks. | Full Analysis Set: : all participants registered, with the exception of those who had not received any dose of the investigational product and those who had no efficacy assessment after administration of the investigational product | Posted | | Number | | Participants | | Week 24 | | | | ID | Title | Description |
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| OG000 | GSK1325760A | GSK1325760A 5 mg once a day by Week 12. After Week 12, GSK1325760A 10 mg once a day (the dosage could be increased or decreased appropriately according to a participant's condition) |
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| Secondary | Mean Change From Baseline in Mean Pulmonary Atery Pressure (mPAP) and Mean Right Atrial Pressure (mRAP) at Weeks 12 and 24 | mPAP and mRAP are measures of cardiopulmonary hemodynamics. Change from baseline was calculated as the Week 12 and 24 values minus the baseline value. Observed data analysis (no imputation techniques). | Full Analysis Set: Analysis was conducted using observed data only. Some participants were withdrawn before Week 24, or some participants could not be measured at Week 24 in this study. | Posted | | Mean | Standard Deviation | mmHg | | Baseline and Weeks 12 and 24 | | | | ID | Title | Description |
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| OG000 | GSK1325760A | GSK1325760A 5 mg once a day by Week 12. After Week 12, GSK1325760A 10 mg once a day (the dosage could be increased or decreased appropriately according to a participant's condition) |
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| Secondary | Mean Change From Baseline in Cardiac Index (CI) at Weeks 12 and 24 | CI is a measure of cardiopulmonary hemodynamics. Change from baseline was calculated as the Week 12 and 24 values minus the baseline value. Observed data analysis (no imputation techniques). | Full Analysis Set: Analysis was conducted using observed data only. Some participants were withdrawn before Week 24, or some participants could not be measured at Week 24 in this study. | Posted | | Mean | Standard Deviation | L/min/m2 | | Baseline and Weeks 12 and 24 | | | | ID | Title | Description |
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| OG000 | GSK1325760A | GSK1325760A 5 mg once a day by Week 12. After Week 12, GSK1325760A 10 mg once a day (the dosage could be increased or decreased appropriately according to a participant's condition) |
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| Secondary | Mean Change From Baseline in Cardiac Output (CO) at Weeks 12 and 24 | CO is a measure of cardiopulmonary hemodynamics. Change from baseline was calculated as the Week 12 and 24 values minus the baseline value. Observed data analysis (no imputation techniques). | Full Analysis Set: Analysis was conducted using observed data only. Some participants were withdrawn before Week 24, or some participants could not be measured at Week 24 in this study. | Posted | | Mean | Standard Deviation | L/min | | Baseline and Weeks 12 and 24 | | | | ID | Title | Description |
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| OG000 | GSK1325760A | GSK1325760A 5 mg once a day by Week 12. After Week 12, GSK1325760A 10 mg once a day (the dosage could be increased or decreased appropriately according to a participant's condition) |
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| Secondary | Mean Change From Baseline in Pulmonary Vascular Resistance (PVR) at Weeks 12 and 24 | PVR is a measure of cardiopulmonary hemodynamics. Change from baseline was calculated as the Week 12 and 24 values minus the baseline value. Observed data analysis (no imputation techniques). | Full Analysis Set: Analysis was conducted using observed data only. Some participants were withdrawn before Week 24, or some participants could not be measured at Week 24 in this study. | Posted | | Mean | Standard Deviation | mmHg/L/min | | Baseline and Weeks 12 and 24 | | | | ID | Title | Description |
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| OG000 | GSK1325760A | GSK1325760A 5 mg once a day by Week 12. After Week 12, GSK1325760A 10 mg once a day (the dosage could be increased or decreased appropriately according to a participant's condition) |
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| Secondary | Mean Change From Baseline in B-type Natriuretic Peptide (BNP) Values at Weeks 12 and 24 | Change from baseline was calculated as the Week 12 and 24 values minus the baseline value. BNP is a surrogate maker of heart failure and was measured by a central laboratory. Observed data analysis (no imputation techniques). | Full Analysis Set: Analysis was conducted using observed data only. Some participants were withdrawn before Week 24, or some participants could not be measured at Week 24 in this study. | Posted | | Mean | Standard Deviation | Nanograms/Liter (ng/L) | | Baseline and Weeks 12 and 24 | | | | ID | Title | Description |
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| OG000 | GSK1325760A | GSK1325760A 5 mg once a day by Week 12. After Week 12, GSK1325760A 10 mg once a day (the dosage could be increased or decreased appropriately according to a participant's condition) |
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