Study to evaluate the efficacy and safety of different doses of Bay 63-2521 in patients with Chronic Thromboembolic Pulmonary Hypertension (CTEPH).

• Register: EUCTR
• Last refreshed on: 25 November 2019
• Main ID: EUCTR2007-000072-16-GB
• Date of registration: 17/10/2008
• Prospective Registration: Yes
• Primary sponsor: Bayer HealthCare AG, D-51368 Leverkusen
• Public title: Study to evaluate the efficacy and safety of different doses of Bay 63-2521 in patients with Chronic Thromboembolic Pulmonary Hypertension (CTEPH).
• Scientific title: Randomized, double-blind, placebo-controlled, multi-centre, multi-national study to evaluate the efficacy and safety of oral BAY 63-2521 (1 mg, 1.5 mg, 2 mg, or 2.5 mg tid) in patients with Chronic Thromboembolic Pulmonary Hypertension (CTEPH). - CHEST-1 Study
• Date of first enrolment: 09/03/2009
• Target sample size: 270
• Recruitment status: Not Recruiting
• URL: https://www.clinicaltrialsregister.eu/ctr-search/search?query=eudract_number:2007-000072-16
• Study type: Interventional clinical trial of medicinal product
• Study design: Controlled: yes; Randomised: yes; Open: no; Single blind: no; Double blind: yes; Parallel group: yes; Cross over: no; Other: no; If controlled, specify comparator, Other Medicinial Product: no; Placebo: yes; Other: no; Number of treatment arms in the trial: 2
• Phase: Human pharmacology (Phase I): no Therapeutic exploratory (Phase II): no Therapeutic confirmatory - (Phase III): yes Therapeutic use (Phase IV): no

Countries of recruitment

Argentina, Australia, Austria, Belgium, Brazil, Canada, China, Czech Republic, Denmark, France, Germany, Ireland, Israel, Italy, Japan, Korea, Republic of, Netherlands, Poland, Portugal, Russian Federation, Slovakia, Spain, Switzerland, Taiwan, Turkey, United Kingdom, United States

Contacts

• Name: CTP Team/REF. 'EU-CTR'/S102-R
• Affiliation: Bayerhealthcare AG

• Name: CTP Team/REF. 'EU-CTR'/S102-R
• Affiliation: Bayerhealthcare AG

Key inclusion & exclusion criteria

Inclusion criteria:
• 18 to 80 years of age at Visit 1 (please consider age related restrictions with respect to the baseline PCWP see section 4.2.3. Cardiovascular Exclusion Criteria).
The lower age limit may be higher if legally requested in the participating countries.
• Male and female patients with CTEPH and an eligibility and baseline 6MWD Test between 150 m and 450 m either defined as :
o Inoperable, with pulmonary vascular resistance >300 dyn*sec*cm-5 measured at least 90 days after start of full anticoagulation and mean pulmonary artery pressure >25 mmHg
The inoperability of CTEPH patients, considered as ineligible for Pulmonary Endarterectomy (PEA), needs to be confirmed (for details please refer to section 10.14 Operability Assessment).
or
o with persisting or recurrent PH after Pulmonary Endarterectomy (Patients must have a PVR >300 dyn*sec*cm-5 measured at least 180 days after surgery)
For patients with persisting or recurrent PH after PEA no study related operability assessment must be performed. Patients that have been assessed as being operable during screening and underwent PEA, may be included again into the study when subsequently recurrent or persisting PH is diagnosed (Note: patients with evidence for recurrent thromboembolism are excluded from the trial / see Section 4.2.3 "Cardiovascular Exclusions").
Note: With respect to the verification of the inclusion criteria, PAPmean and PVR are considered as calculated parameters. For the respective calculations refer to sections 4.6.4 and 10.5.
• Unspecific treatments which may also be used for the treatment of pulmonary hypertension such as oral anticoagulants, diuretics, digitalis, calcium channel blockers or oxygen supplementation are permitted. However, treatment with anticoagulants must have been started at least 90 days before Visit 1 and treatment with diuretics needs to be stable for at least 30 days before Visit 1.
• Patients with supplemental long-term oxygen therapy can be included, if the amount of supplemental oxygen and the delivery method was stable for at least 90 days before Visit 1.
• Right-heart catheterization results for the definite diagnosis of PH must not be older than 8 weeks at Visit 1 (will be considered as baseline values), must have been measured after at least 90 days of full anticoagulation, and must have been measured in collaboration with the participating centre under standardized conditions (refer to the study specific Right Heart Catheterization Manual). If the respective measurements have not been performed in context with the patient’s regular diagnostic work up, they have to be performed as a part of the study during the Pre-Treatment Phase (after the patient signed the informed consent) or at Visit 1 before randomization.
• Women without childbearing potential defined as postmenopausal women (= permanent absence of monthly periods for more than 2 years), women with bilateral tubal ligation, women with bilateral ovarectomy, and women with hysterectomy can be included in the study. Women with childbearing potential can only be included in the study if a serological pregnancy test is negative and a combination of safe contraception methods is used throughout the study.
• Patients who are able to understand and follow instructions a
Exclusion criteria:
• Patients unable to perform a valid 6MWD Test (e.g. patients with a severe peripheral artery occlusive disease).
Note: Patients who require walking aids may be included if in the opinion of the investigator the walking distance is not impaired.
• Patients with a relative difference (i.e. absolute difference / mean) of more than 15% between the eligibility- and the baseline 6MWD test (for further details see section 4.6.3).

Medication/Treatment Exclusions:
Patients who are screened for possible participation in the study must not been withdrawn from treatments which are medically required. If such treatments are not in-line with the entry criteria of this study, the patient must not be enrolled.
The following specific medications are not allowed:
Pre-Treatment with the following specific medications is not allowed(a):
• Pre-treatment with NO donors (e.g. Nitrates) within the last 90 days before Visit 1
• Pre-treatment with PAH specific medications:
o Endothelin Receptor Antagonists
o Prostacycline Analogues
o Specific (e.g. Sildenafil or Tadalafil) or unspecific Phosphodiesterase Inhibitors (e.g. Dipyridamole, Theophylline).

Pulmonary Disease Exclusions:
• All types of pulmonary hypertension except subtypes 4.1 and 4.2 of the Venice Clinical Classification of Pulmonary Hypertension
• Moderate to severe obstructive lung disease (Forced Expiratory Volume in one second < 60% predicted)
The predicted Forced Expiratory Volume in one second (FEV1) is a calculated value. For the calculation refer to section 10.4
• Severe restrictive lung disease (Total Lung Capacity <70% predicted).
The predicted Total Lung Capacity (TCL) is a calculated value. For the calculation refer to section 10.4
• Severe congenital abnormalities of the lungs, thorax, and diaphragm.

Exclusions related to abnormalities in blood gases (capillary or arterial at rest):
• SaO2 < 88% at Visit 0 despite supplemental oxygen therapy.
• PaO2 < 55 mmHg at Visit 0 despite supplemental oxygen therapy.
• PaCO2 > 45 mmHg at Visit 0.

Cardiovascular Exclusions:
• History of uncontrolled arterial hypertension within the last 90 days before Visit 1 and/or
• Systolic blood pressure > 180 mmHg and/or diastolic blood pressure > 110 mmHg at Visit 0 and/or Visit 1 before randomisation.
• History of uncontrolled arterial hypotension within the last 90 days before Visit 1 and/or
• Systolic blood pressure <95 mmHg at Visit 0 and/or Visit 1 before randomisation.
• Resting heart rate in the awake patient <50 BPM or >105 BPM at Visit 0 and/or Visit 1 before randomisation.
• Atrial fibrillation / atrial flutter within the last 90 days before Visit 1.
• Left heart failure with an ejection fraction less than 40% within the last 90 days before Visit 1.
• Pulmonary venous hypertension indicated by baseline pulmonary capillary wedge pressure >15 mmHg (if age is between 18 and 75 years at Visit 1) or > 12 mmHg (if age is > 75 years at Visit 1).
• Hypertrophic obstructive cardiomyopa

Age minimum:
Age maximum:
Gender:
Female: yes
Male: yes

Health Condition(s) or Problem(s) studied

Chronic Thromboembolic Pulmonary Hypertension
MedDRA version: 14.0 Level: PT Classification code 10037400 Term: Pulmonary hypertension System Organ Class: 10038738 - Respiratory, thoracic and mediastinal disorders

Therapeutic area: Diseases [C] - Cardiovascular Diseases [C14]

Intervention(s)

Product Name: BAY 63-2521 tablets 0.5 mg
Product Code: BAY 63-2521
Pharmaceutical Form: Film-coated tablet
INN or Proposed INN: riociguat
CAS Number: 625115-55-1
Current Sponsor code: BAY 63-2521
Other descriptive name: Methyl 4,6-diamino-2-[1-(2-fluorobenzyl)-1H-pyrazolo [3,4-b]pyridine-3-yl]-5-pyrimidinyl(methyl)carb
Concentration unit: mg milligram(s)
Concentration type: equal
Concentration number: 0.5-
Pharmaceutical form of the placebo: Film-coated tablet
Route of administration of the placebo: Oral use

Product Name: BAY 63-2521 tablets 1 mg
Product Code: BAY 63-2521
Pharmaceutical Form: Film-coated tablet
INN or Proposed INN: riociguat
CAS Number: 625115-55-1
Current Sponsor code: BAY 63-2521
Other descriptive name: Methyl 4,6-diamino-2-[1-(2-fluorobenzyl)-1H-pyrazolo [3,4-b]pyridine-3-yl]-5-pyrimidinyl(methyl)carb
Concentration unit: mg milligram(s)
Concentration type: equal
Concentration number: 1-
Pharmaceutical form of the placebo: Film-coated tablet
Route of administration of the placebo: Oral use

Product Name: BAY 63-2521 tablets 1.5 mg
Product Code: BAY 63-2521
Pharmaceutical Form: Film-coated tablet
INN or Proposed INN: riociguat
CAS Number: 625115-55-1
Current Sponsor code: BAY 63-2521
Other descriptive name: Methyl 4,6-diamino-2-[1-(2-fluorobenzyl)-1H-pyrazolo [3,4-b]pyridine-3-yl]-5-pyrimidinyl(methyl)carb
Concentration unit: mg milligram(s)
Concentration type: equal
Concentration number: 1.5-
Pha

Primary Outcome(s)

Timepoint(s) of evaluation of this end point: 6MWD: Baseline (pre-treatment), Day 14, Day 28, Day 42, day 56, Day 84, Day 112

Main Objective: To assess the efficacy and safety of oral BAY 63-2521 in patients with inoperable Chronic Thromboembolic Pulmonary Hypertension (CTEPH) or recurrent or persisting pulmonary hypertension after surgical treatment. The optimized dose reached after individual dose titration (starting with 1 mg tid and if tolerated up-titrated after two weeks up to 1.5 mg or 2 mg or 2.5 mg tid) will be compared with placebo.

Secondary Objective: Secondary efficacy endpoints are:
- Change from Baseline in Pulmonary Vascular Resistance (PVR) after 16
weeks
- Change from baseline in NT-pro BNP after 16 weeks
- Change from baseline in WHO functional class after 16 weeks
-Time To Clinical Worsening
- Change from baseline in Borg CR 10 Scale or Modified Borg Dyspnoea (if patients were enrolled before amendment 3 approval in their countries) measured at the end of the 6MWD Test after 16 weeks
-Change from baseline in EQ-5D questionnaire after 16 weeks
- Change from baseline in LPH questionnaire after 16 weeks

Primary end point(s): The primary endpoint is change from baseline in 6 Minute Walking Distance (6MWD) after 16 weeks.

Secondary Outcome(s)

Timepoint(s) of evaluation of this end point: Baseline (pre-treatment), Day 14, Day 28, Day 42, day 56, Day 84, Day 112 for all. 30 days post treatment stop EQ-5D and LPH questionnaires.

Secondary end point(s): Change from baseline in PVR, NT-pro BNP, WHO functional class, EQ-5D questionnaire, and LPH questionnaire after 16 weeks, time to clinical worsening, change from baseline in Borg CR 10 scale or modified Borg Dyspnoea measured at the end of the 6MWD after 16 weeks

Secondary ID(s)

BAY 63-2521/11348

2007-000072-16-DE

Source(s) of Monetary Support

Bayer Pharma AG

Ethics review

Status: Approved
Approval date:
Contact:

Results

• Results available: Yes
• Date Posted: 05/11/2014
• Date Completed: 27/06/2012
• URL: https://www.clinicaltrialsregister.eu/ctr-search/trial/2007-000072-16/results