Trial Condition(s):
Heart failure (HF)
A trial to study BAY1753011 in patients with Congestive Heart Failure (AVANTI)
Bayer Identifier:
17909
ClinicalTrials.gov Identifier:
EudraCT Number:
Not Available
EU CT Number:
Not Available
Propósito del ensayo
To assess the efficacy of 30 mg of BAY1753011, with or without furosemide, versus furosemide alone in patients with heart failure and objective evidence of congestion.
Criterios de inclusión
: - History of CHF on individually optimized treatment with HF medications unless contraindicated or not tolerated, for at least 12 weeks prior to index hospitalization and in accordance with international guidelines. - Subjects admitted to the hospital with a primary diagnosis of decompensated HF including symptoms and signs of fluid overload requiring IV diuretic therapy in the Emergency room (ER) or any time between day 1-3 of hospital admission (index hospitalization). - Subjects on an average/usual total daily dose of loop diuretic ≥ 40 mg of furosemide or equivalent, within 4 weeks prior to index hospitalization. - At least one of the following 5 parameters any day between 3-7 of index hospitalization (screening period) -- Natriuretic peptides Brain natriuretic peptide/N-terminal prohormone of brain natriuretic peptide (BNP/NT-proBNP): --- Drop in BNP or NT-proBNP ≤ 30% from admission values (if measured during index hospitalization) or --- BNP ≥ 500 pg/ml or NT-proBNP ≥ 1800 pg/ml at screening (day 3 to 7 of index hospitalization) -- Body weight (BW) loss <0.4 kg per 40 mg furosemide at day 4 of index hospitalization -- Composite congestion score (CCS) ≥ 3 -- Hypervolemic hyponatremia defined as serum sodium < 136 mmol/l -- In hospital worsening renal function defined as increased serum creatinine ≥ 0.3 mg/dl compared to index hospitalization admission values AND at least one the following --- Jugular venous pressure (JVP) ≥ 10 cm on physical examination --- Inferior vena cava (IVC) diameter > 21 mm --- IVC collapse with sniff < 50% --- At least 2+ peripheral edema or pulmonary edema or pleural effusion on chest X-ray or clinical exam
Criterios de exclusión
- Active or history of acute inflammatory heart disease, within 3 months prior to screening, e.g., acute myocarditis - Acute coronary syndrome, including unstable angina, Non-ST segment elevation myocardial infarction (NSTEMI) or ST segment elevation myocardial infarction (STEMI), or major Cardiovascular (CV) surgery including coronary artery bypass graft (CABG), percutaneous coronary intervention (PCI) within 3 months prior to screening - Any primary cause of HF scheduled for surgery or interventional therapy (e.g., TAVI), e.g., valve disease such as severe aortic stenosis or mitral valve regurgitation - Requirement of mechanical support (intra-aortic balloon pump, endotracheal intubation, mechanical ventilation, or any ventricular assist device) or ultrafiltration/hemodialysis - Estimated glomerular filtration rate of < 30 ml/min/1.73 m*2 determined by the Modified Diet and Renal Disease equation at screening; reassessments allowed as clinically needed - Serum potassium ≥ 5.5 mmol/L or ≤ 3.3 mmol/L at screening; reassessments allowed as clinically needed - Serum sodium ≥ 146 mmol/L or ≤ 130 mmol/L at screening; reassessments allowed as clinically needed - Concomitant treatment with potassium-sparing diuretic (with the exception of mineralocorticoid- receptor antagonist (MRA) that cannot be stopped prior to randomization and for the duration of the treatment period.
Resumen del ensayo
Enrollment Goal
Trial Dates
Phase
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Accepts Healthy Volunteers
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| Ubicaciones | Estado | |
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Diseño del ensayo
A Multicenter, Randomized, Parallel Group, Double Blind, Active and Placebo Controlled Study of BAY1753011, a Dual V1a/V2 Vasopressin Receptor Antagonist, in Patients with Congestive Heart Failure: AVANTI Study
Trial Type:
Interventional
Intervention Type:
Drug
Trial Purpose:
Treatment
Allocation:
Randomized
Blinding:
N/A
Assignment:
Parallel Assignment
Trial Arms:
6
Primary Outcome
- PART A: Change in body weightTimeframe: Compare Day 30 (End of part A) with Day 1 (Start of part A)
- PART A: Change in serum creatinineTimeframe: Compare Day 30 (End of part A) with Day 1 (Start of part A)
- PART B: Change in body weightTimeframe: Compare Day 60 (End of part B) with Day 30 (Start of part B)
- PART B: Change in BUN/creatinine ratioBUN:Blood urea nitrogenTimeframe: Compare Day 60 (End of part B) with Day 30 (Start of part B)
Secondary Outcome
- Incidence of Treatment-emergent adverse event (including Serious adverse event)Timeframe: Up to 60 days
- Change in augmentation indexTimeframe: Up to 60 days
Información adicional
Not Available
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