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Study on the Safety of BAY1817080, How it is Tolerated and the Way the Body Absorbs, Distributes and Gets Rid of the Study Drug in Participants With Impaired Liver Function or Normal Liver Function

Phase 1
Completed
Conditions
Overactive Bladder
Diabetic Neuropathic Pain
Refractory or Unexplained Chronic Cough
Endometriosis Related Pain
Interventions
Registration Number
NCT04454424
Lead Sponsor
Bayer
Brief Summary

BAY1817080 is currently under clinical development to treat pain related to unexplained chronic cough or chronic cough not affected by a treatment (refractory and/or unexplained chronic cough, RUCC), or a condition where the bladder is unable to hold urine normally (overactive bladder, OAB) or a condition in which tissue similar to the tissue that normally lines the inside of the womb grows outside the womb (endometriosis).

In this study researchers want to learn more about the safety of BAY1817080, how it is tolerated and the way the body absorbs, distributes and gets rid of the study dug given as tablet in participants with mild, moderate or severe hepatic impairment and participants with normal liver function matched for age-, gender-, weight and race.

The study will enroll 36 male and female participants in the age between 18 and 79 years. Participants with mild or moderate hepatic impairment and the matching participants will take multiple oral doses of study drug depending on the study plan. Participants with severe hepatic impairment and the matching participants will take a single oral dose of study drug during the study. Data from this study will provide researcher important information for further development of the study drug in particular on dose recommendation for patients with hepatic impairment.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
37
Inclusion Criteria
  • Participant must be 18 to 79 years of age inclusive, at the time of signing the informed consent.

  • Participants with a medical history of chronic (For Hepatically Impaired Participants only):

    • documented liver cirrhosis confirmed by histopathology, laparoscopy, fibroscan, CT, MRI or ultrasound, AND
    • hepatic impairment (Child-Pugh A or B or C), AND
    • stable liver disease, i.e. same Child-Pugh class for at least 2 months prior to screening.
  • Body mass index (BMI) within the range 18 to 38 kg/m^2 (both inclusive).

  • Male or female.

  • Women of childbearing potential (WOCBP) must agree to use contraception for the duration of the study. This applies for the time period between signing of the Informed Consent Form until at least 30 days after the last dose of the study drug.

  • Capable of giving signed informed consent as described in study protocol which includes compliance with the requirements and restrictions listed in the informed consent form (ICF) and in this protocol.

Exclusion Criteria
  • Any relevant disease (other than those related to hepatic impairment for the hepatic impaired participants) within 4 weeks prior to study drug administration including infections and acute gastro-intestinal diseases (vomiting, diarrhea, constipation) requiring medical treatment.
  • Renal failure with an estimated glomerular filtration rate (eGFR) ≤ 35 mL/min, according to Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation.
  • Use of strong CYP3A4 and P-glycoprotein inhibitors from 2 weeks before study treatment until last day of blood sampling for pharmacokinetics after study drug administration.
  • Use of CYP3A4 and P-glycoprotein inducers from 2 weeks before study treatment until last day of blood sampling for pharmacokinetics after study drug administration.
  • Use of drugs which may affect absorption (e.g. loperamide, metoclopramide), and systemic administration of any broad-spectrum antibiotic within 1 week before first study drug administration, unless the drug is part of the mandatory dosing regimen for treatment of hepatic impairment or related conditions.
  • Indication or evidence for long QT syndrome; Participants in control arm only: QT interval corrected using Fridericia's method (QTcF) > 450 msec.
  • Ascites qualitatively estimated as severe ascites by physical examination, with need of paracentesis; or a recent history of paracentesis.
  • Alkaline phosphatase (AP) ≥4 times the upper limit of normal (ULN).
  • Aspartate aminotransferase (AST) or alanine aminotransferase (ALT) in conjunction with gamma-glutamyl transpeptidase (GGT) ≥4 times the ULN (an isolated elevation of GGT above 4 times ULN will not exclude the participant).
  • International Normalized Ratio (INR) > 2.7.
  • Inability to provide informed consent: Participants with psychiatric disorders, including hepatic encephalopathy >grade 2, e.g. number connection test >80 seconds.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Arm A: Child-Pugh ABAY1817080Participants with mildly impaired hepatic function (Child-Pugh A)
Arm E: Normal hepatic (Matched to C)BAY1817080Participants with normal hepatic function matched to Arm C
Arm C: Child-Pugh CBAY1817080Participants with severely impaired hepatic function (Child-Pugh C)
Arm D: Normal hepatic (Matched A and B)BAY1817080Participants with normal hepatic function matched to Arm A and B
Arm B: Child-Pugh BBAY1817080Participants with moderately impaired hepatic function (Child-Pugh B)
Arm D: Normal hepatic (Matched A and B)MidazolamParticipants with normal hepatic function matched to Arm A and B
Arm A: Child-Pugh AMidazolamParticipants with mildly impaired hepatic function (Child-Pugh A)
Arm B: Child-Pugh BMidazolamParticipants with moderately impaired hepatic function (Child-Pugh B)
Arm C: Child-Pugh CMidazolamParticipants with severely impaired hepatic function (Child-Pugh C)
Arm E: Normal hepatic (Matched to C)MidazolamParticipants with normal hepatic function matched to Arm C
Primary Outcome Measures
NameTimeMethod
AUCu after single dose of BAY1817080On day 1

AUCu: Area under the Curve unbound

Cmax,u after single dose of BAY1817080On day 1

Cmax,u: maximum observed drug concentration in measured matrix after single dose administration (unbound)

Secondary Outcome Measures
NameTimeMethod
Cmax,md,u after multiple dose of BAY1817080From day 6 to day 13

Cmax,md,u: Maximum observed drug concentration at steady state for multiple dose (unbound)

Number of subjects with treatment-emergent adverse eventsfrom dosing up to 14 days after end of treatment with study medication
AUC (0-12)md,u after multiple dose of BAY1817080From day 6 to day 13

AUC (0-12)md,u: Area Under the Curve from 0-12 hours at steady state for the multiple dose (unbound)

Trial Locations

Locations (2)

Orlando Clinical Research Center

🇺🇸

Orlando, Florida, United States

Clinical Pharmacology of Miami, LLC

🇺🇸

Miami, Florida, United States

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