E.1 Medical condition or disease under investigation |
E.1.1 | Medical condition(s) being investigated |
Chronic Thromboembolic Pulmonary Hypertension, inoperable or persistent/recurrent |
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E.1.1.1 | Medical condition in easily understood language |
Chronic Thromboembolic Pulmonary Hypertension (CTEPH) is a disease associated with abnormally high pressure in the blood vessels of the lungs, caused by the formation of blood clots. |
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E.1.1.2 | Therapeutic area | Diseases [C] - Respiratory Tract Diseases [C08] |
MedDRA Classification |
E.1.2 Medical condition or disease under investigation |
E.1.2 | Version | 20.0 |
E.1.2 | Level | LLT |
E.1.2 | Classification code | 10068739 |
E.1.2 | Term | Chronic thromboembolic pulmonary hypertension |
E.1.2 | System Organ Class | 100000004855 |
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E.1.3 | Condition being studied is a rare disease | Yes |
E.2 Objective of the trial |
E.2.1 | Main objective of the trial |
The primary objective of the study is to evaluate the effect of selexipag on pulmonary vascular resistance (PVR) versus placebo in subjects with inoperable CTEPH and persistent/recurrent CTEPH after surgical treatment (pulmonary endarterectomy [PEA] and/or balloon pulmonary angioplasty [BPA]) at Week 20.
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E.2.2 | Secondary objectives of the trial |
The secondary objectives of the study are to evaluate the effects of selexipag versus placebo on: • Exercise capacity • Rate of death or hospitalizations related to Pulmonary Hypertension (PH) worsening. • Time to clinical worsening • WHO functional class (FC) • Patient-reported outcomes (PROs) • Dyspnea • N-terminal pro b-type natriuretic peptide (NT-proBNP). |
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E.2.3 | Trial contains a sub-study | No |
E.3 | Principal inclusion criteria |
1. Signed and dated ICF. 2. Male and female subjects ≥18 and ≤ 85 years old. 3. Subjects with CTEPH, as confirmed by the corresponding adjudication committee (AC; country-specific adjudication committee [CSAC] or central adjudication committee [CAC]), defined as one of the following options: a) Inoperable CTEPH with: – Diagnosis of CTEPH based on at least two of the following assessments performed in the 14-month period prior to randomization (Visit 2): ventilation/perfusion (V/Q) scan; pulmonary angiography (PA); computed tomography pulmonary angiogram (CTPA) and/or magnetic resonance angiography (MRA). – RHC1 performed at least 90 days after start of full anticoagulation showing: PVR at rest ≥ 300 dyn.sec/cm5; Mean pulmonary artery pressure (mPAP) ≥ 25 mmHg; Pulmonary arterial wedge pressure (PAWP) ≤ 15 mmHg or, if not available or unreliable, a left ventricular end diastolic pressure (LVEDP) ≤ 15 mmHg. b) Persistent/recurrent CTEPH after BPA, with: – Diagnosis of CTEPH based on at least one of the following assessments performed in the 14-month period prior to randomization (Visit 2): V/Q scan, PA, CTPA or MRA. – RHC1 performed at least 90 days after surgery and at least 90 days after start of full anticoagulation showing: PVR at rest ≥ 300 dyn.sec/cm5; mPAP ≥ 25 mmHg; PAWP ≤ 15 mmHg, or, if not available or unreliable, an LVEDP ≤ 15 mmHg. c) Persistent/recurrent PH after PEA (including PEA followed by BPA) with: – RHC1 performed at least 90 days after surgery and at least 90 days after start of full anticoagulation showing: PVR at rest ≥ 300 dyn.sec/cm5; mPAP ≥ 25 mmHg; PAWP ≤ 15 mmHg, or, if not available or unreliable, an LVEDP ≤ 15 mmHg. 4. Symptomatic PH in WHO FC I–IV. 5. Subject able to perform the 6MWT with a minimum distance of 100 m and a maximum distance of 450 m at screening visit (Visit 1).
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E.4 | Principal exclusion criteria |
General exclusion criteria: 1. Planned or current treatment with another investigational treatment up to 3 months prior to randomization. 2. Any known factor or disease that might interfere with treatment compliance, study conduct, or interpretation of the results, such as drug or alcohol dependence or psychiatric disease. 3. Known concomitant life-threatening disease with a life expectancy < 12 months.
Exclusion criteria related to the disease: 4. Planned BPA within 26 weeks after randomization. 5. Change in dose or initiation of new PH-specific therapy within 90 days prior to randomization. 6. Treatment with prostacyclin (epoprostenol), prostacyclin analogs (i.e., treprostinil, iloprost, beraprost) or prostacyclin receptor agonists (i.e., selexipag) within 90 days prior to randomization. 7. Change in dose or initiation of new diuretics and/or calcium channel blockers within 1 week prior to baseline RHC.
Exclusion criteria related to comorbidities: 8. Any co-morbid condition that may influence the ability to perform a reliable and reproducible 6MWT, including use of walking aids (cane, walker, etc). 9. Other as per selexipag Summary of Product Characteristics (SmPC).
Exclusion criteria related to selexipag use: 10. As per selexipag Summary of Product Characteristics (SmPC). |
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E.5 End points |
E.5.1 | Primary end point(s) |
The primary efficacy endpoint of this study is the pulmonary vascular resistance (PVR) at Week 20, assessed at rest, within 2–5 hours post-dose, expressed as percent of baseline PVR. |
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E.5.1.1 | Timepoint(s) of evaluation of this end point |
Assessed at rest in screening period (Day -60 to Day -14; baseline) and assessed at rest within 2–5 hours post-dose at Week 20 during treatment period. |
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E.5.2 | Secondary end point(s) |
1. Change from baseline in 6-minute walk distance (6MWD) to Week 26 (key secondary endpoint). 2. Rate of all-cause death or hospitalizations related to PH worsening up to Week 52. 3. Time to clinical worsening up to Week 52, defined as at least one of the following components: – All-cause death – Non-planned PH-related hospitalization – PH-related deterioration (identified by: Increase in WHO FC; Deterioration by at least 15% in exercise capacity, as measured by the 6MWD; Signs or symptoms of right heart failure, defined as a reported AE with one of the preferred terms "CTEPH”, “pulmonary hypertension”, “right ventricular failure”, “right ventricular dysfunction” and/or “acute right ventricular failure”). 4. Proportion of subjects with improvement in WHO FC from baseline to Week 26. 5. Change from baseline to Week 26 in PAH-SYMPACT™ scores. 6. Change from baseline to Week 26 in Borg dyspnea index (BDI) scores. 7. Change from baseline to Week 26 in NT-proBNP. |
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E.5.2.1 | Timepoint(s) of evaluation of this end point |
1. and 4.-7.: at Day 1, Week12, Week20, Week26 during treatment period. 2. and 3.: at Day 1, Week12, Week20, Week26, Week39 and Week52 during treatment period.
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E.6 and E.7 Scope of the trial |
E.6 | Scope of the trial |
E.6.1 | Diagnosis | No |
E.6.2 | Prophylaxis | No |
E.6.3 | Therapy | No |
E.6.4 | Safety | Yes |
E.6.5 | Efficacy | Yes |
E.6.6 | Pharmacokinetic | No |
E.6.7 | Pharmacodynamic | No |
E.6.8 | Bioequivalence | No |
E.6.9 | Dose response | No |
E.6.10 | Pharmacogenetic | No |
E.6.11 | Pharmacogenomic | No |
E.6.12 | Pharmacoeconomic | No |
E.6.13 | Others | No |
E.7 | Trial type and phase |
E.7.1 | Human pharmacology (Phase I) | No |
E.7.1.1 | First administration to humans | No |
E.7.1.2 | Bioequivalence study | No |
E.7.1.3 | Other | No |
E.7.1.3.1 | Other trial type description | |
E.7.2 | Therapeutic exploratory (Phase II) | No |
E.7.3 | Therapeutic confirmatory (Phase III) | Yes |
E.7.4 | Therapeutic use (Phase IV) | No |
E.8 Design of the trial |
E.8.1 | Controlled | Yes |
E.8.1.1 | Randomised | Yes |
E.8.1.2 | Open | No |
E.8.1.3 | Single blind | No |
E.8.1.4 | Double blind | Yes |
E.8.1.5 | Parallel group | Yes |
E.8.1.6 | Cross over | No |
E.8.1.7 | Other | Yes |
E.8.1.7.1 | Other trial design description |
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E.8.2 | Comparator of controlled trial |
E.8.2.1 | Other medicinal product(s) | No |
E.8.2.2 | Placebo | Yes |
E.8.2.3 | Other | No |
E.8.2.4 | Number of treatment arms in the trial | 2 |
E.8.3 |
The trial involves single site in the Member State concerned
| No |
E.8.4 | The trial involves multiple sites in the Member State concerned | Yes |
E.8.4.1 | Number of sites anticipated in Member State concerned | 4 |
E.8.5 | The trial involves multiple Member States | Yes |
E.8.5.1 | Number of sites anticipated in the EEA | 57 |
E.8.6 Trial involving sites outside the EEA |
E.8.6.1 | Trial being conducted both within and outside the EEA | Yes |
E.8.6.2 | Trial being conducted completely outside of the EEA | No |
E.8.6.3 | If E.8.6.1 or E.8.6.2 are Yes, specify the regions in which trial sites are planned |
Australia |
Austria |
Belgium |
Brazil |
Bulgaria |
Canada |
China |
Czech Republic |
Denmark |
Estonia |
Finland |
Germany |
Greece |
Hong Kong |
Hungary |
Israel |
Italy |
Korea, Republic of |
Latvia |
Lithuania |
Mexico |
Netherlands |
Poland |
Portugal |
Russian Federation |
Singapore |
Slovakia |
South Africa |
Spain |
Sweden |
Switzerland |
Taiwan |
Thailand |
Turkey |
Ukraine |
United Kingdom |
United States |
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E.8.7 | Trial has a data monitoring committee | Yes |
E.8.8 |
Definition of the end of the trial and justification where it is not the last
visit of the last subject undergoing the trial
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E.8.9 Initial estimate of the duration of the trial |
E.8.9.1 | In the Member State concerned years | 3 |
E.8.9.1 | In the Member State concerned months | 3 |
E.8.9.1 | In the Member State concerned days | |
E.8.9.2 | In all countries concerned by the trial years | 3 |
E.8.9.2 | In all countries concerned by the trial months | 3 |