check_circleStudy Completed

Congestive heart failure, Renal impairment

Bayer Identifier:

19482

ClinicalTrials.gov Identifier:

NCT05599997

EudraCT Number:

2019-000876-41

EU CT Number:

Not Available
A study to learn how the study treatment BAY1753011 moves into, through and out of the body, how it works, how safe it is, and how it affects the body when given once as tablet in male and female participants with reduced kidney function compared to matched participants with normal kidney function

Trial purpose

Researchers are looking for a better way to treat people with heart failure.
Heart failure is a condition which occurs when the heart does not pump blood as well as it should leading to shortness of breath, tiredness, and ankle swelling.

The study treatment BAY1753011 is under development to treat heart failure. It is thought to reduce the action of a hormone called vasopressin that is naturally produced in the body. People with heart failure often have elevated levels of vasopressin. This is known to result in worsening of the heart failure condition.
People with heart failure often also have reduced kidney functions. As kidneys play a role in removal of drugs from the body, reduced kidney function may result in higher blood levels of BAY1753011.

The main purpose of this study was to learn how BAY1753011 moved into, through and out of the body in participants with different degrees of reduced kidney function compared to matched participants (age, gender, and weight) with normal kidney function.
To answer this, the researchers compared:
• the (average) total level of BAY1753011 in the blood (also called AUC)
• the (average) highest level of BAY1753011 in the blood (also called Cmax)
between the different groups with reduced kidney function (mild/moderate/severe) and the control group (normal kidney function).

In addition, the researchers wanted to know how safe BAY1753011 was and the degree to which overt medical problems caused by it could be tolerated (also called tolerability) by the different groups of participants.
These medical problems are also known as “adverse events”. Doctors keep track of all medical problems that happen in studies, even if they do not think they might be related to the study treatments.

All participants took a single dose of BAY1753011 in tablet form by mouth.
Each participant was in the study for approximately 3 to 4 weeks, including an in-house phase of 5 days and 4 nights with one treatment day.
During the study, the doctors and their study team:
• did physical examinations
• checked vital signs such as blood pressure, heart rate, body temperature and number of breaths within a minute (respiratory rate)
• examined heart health using electrocardiogram (ECG)
• took blood and urine samples
• counted the number of toilet visits during the night

Key Participants Requirements

Sex

All

Age

18 - N/A
  • - Male or female White participants (women without childbearing potential)
    - Aged from ≥18 years
    - body mass index above or equal 18.5 kg/m2 and below or equal 36 kg/m2 at the first screening visit
    - Participants with renal impairment: with an eGFR <90 mL/min/1.73 m^2 determined from serum creatinine 21-3 days prior to dosing using the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation
    - Age-, weight- and gender- matched control group
  • - An anatomical abnormality of the gut that could affect the retention times of the drug in the stomach/gut adversely
    - Conditions or concomitant treatment that might adversely affect the gastric pH level
    - Pancreatic dysfunction/insufficiency
    - Febrile illness within 4 week prior to admission to study center
    - Known hypersensitivity to the study drugs
    - Known severe allergies, non-allergic drug reactions, or multiple drug allergies
    - Participants with a medical disorder, condition or history of such that would impair the participant's ability to participate or complete this study in the opinion of the investigator or the Sponsor
    - Concomitant treatment from 2 weeks before study drug administration until end of follow-up with drugs that may impact the PK of BAY 1753011:Strong and moderate inducers or inhibitors of CYP3A4Moderate and strong inhibitors of P-gp transport Probenecid and valproic acid
    - 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
    - Although no clinical study data are available for BAY 1753011, drugs for the treatment of hyperphosphatemia such as sevelamer or lanthanum should not be given from 24 h before until 24 h after dosing, as they are known to bind many anionic drugs
    - Acute renal failure
    - Active nephritis
    - Severe infection or any clinically significant illness within 4 weeks prior to dosing
    - Impairment of any other major organ system other than the kidney
    - Clinically relevant findings in the ECG such as a second- or third-degree atrioventricular (AV) block, prolongation of the QTc-interval over 480 msec
    - Systolic blood pressure below 100 or above 160 mmHg
    - Diastolic blood pressure below 50 or above 100 mmHg
    - Heart rate below 50 or above 100 beats/ min

Trial summary

Enrollment Goal
32
Trial Dates
November 2019 - May 2021
Phase
Phase 1
Could I Receive a placebo
No
Products
BAY1753011
Accepts Healthy Volunteer
Yes

Where to participate

StatusInstitutionLocation
Completed
CRS Clinical-Research-Services Kiel GmbHKiel, 24105, Germany
Completed
APEX GmbHMünchen, 81241, Germany

Primary Outcome

  • Area under the concentration versus time curve from zero to infinity divided by dose of total BAY1753011 in plasma after single dose administration (AUC/D)
    Dose-normalized AUC (AUC/D) of BAY1753011 was investigated as the dose for the severe renal impairment group was reduced to 15 mg.
    date_rangeTime Frame:
    From pre-dose until 144 hours post dose
  • Maximum observed drug concentration divided by dose of total BAY1753011 in plasma after single dose administration (Cmax/D)
    Dose-normalized Cmax (Cmax/D) of BAY1753011 was investigated as the dose for the severe renal impairment group was reduced to 15 mg.
    date_rangeTime Frame:
    From pre-dose until 144 hours post dose
  • Area under the concentration versus time curve from zero to infinity divided by dose of unbound BAY1753011 in plasma after single dose administration (AUCu/D)
    Dose-normalized AUCu (AUCu/D) of BAY1753011 was investigated as the dose for the severe renal impairment group was reduced to 15 mg.
    date_rangeTime Frame:
    From pre-dose until 144 hours post dose
  • Maximum observed drug concentration divided by dose of unbound BAY1753011 in plasma after single dose administration (Cmax,u/D)
    Dose-normalized Cmax,u (Cmax,u/D) of BAY1753011 was investigated as the dose for the severe renal impairment group was reduced to 15 mg.
    date_rangeTime Frame:
    From pre-dose until 144 hours post dose

Secondary Outcome

  • Number of participants with treatment-emergent adverse events
    date_rangeTime Frame:
    After first application of study medication up to 10 days after the study medication

Trial design

Investigation of pharmacokinetics, pharmacodynamics, safety and tolerability of a single oral dose of 30 mg BAY 1753011 given as IR tablet in male and female participants in a multicenter, non-randomized, non-controlled, non-blinded study with group stratification in participants with renal impairment and control group matched for age-, gender-, and weight
Trial Type
Interventional
Intervention Type
Drug
Trial Purpose
Basic Science
Allocation
Non-randomized
Blinding
N/A
Assignment
Parallel Assignment
Trial Arms
4

Additional Information

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