A Study of ASP0367 in People With Kidneys That do Not Work Well and in Healthy People

  • STATUS
    Recruiting
  • days left to enroll
    61
  • participants needed
    36
  • sponsor
    Astellas Pharma Global Development, Inc.
Updated on 7 October 2022
Investigator
Medical Affairs Europe
Primary Contact
Nucleus Network (3.7 mi away) Contact
+3 other location
Accepts healthy volunteers

Summary

This study is for adults whose kidneys do not work well (renal impairment) and adults whose kidneys work normally. This study will provide more information on a potential new treatment, called ASP0367. The main aim of the study is to learn how ASP0367 is processed by the body in these different groups of people.

This study will be in 2 parts. Part 2 will only happen if the results between the 2 groups are different in Part 1. In each part, people in the study will stay in a research unit for 6 days and 5 nights. Later, they will return to the research unit for 1 check-up.

In Part 1, people whose kidneys work normally and people whose kidneys work very poorly (severe renal impairment) can take part.

If Part 2 happens, people whose kidneys work normally and people whose kidneys do not work well (mild or moderate renal impairment) can take part.

In both parts of the study, people who can take part will be admitted to the research unit. The next day they will take tablets of ASP0367 just once. People will give blood and urine samples at various times during their stay. They will have their vital signs (heart rate and blood pressure) checked regularly. People will also have ECGs to check their heart rhythm. They will be asked if they have any medical problems. After 6 days, provided all the checks have been done and there are no medical problems, people in the study will leave the research unit.

People will return to the research unit for 1 check-up. This will be between 9 and 11 days after their last blood sample was taken during their previous stay in the unit. The check-up will include a physical exam, a check of people's vital signs (heart rate and blood pressure), and blood tests. Also, people will have an ECG and be asked if they have had any medical problems.

Details
Condition Renal Impairment, Healthy Volunteers
Treatment ASP0367
Clinical Study IdentifierNCT05117294
SponsorAstellas Pharma Global Development, Inc.
Last Modified on7 October 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

Participant has a body mass index range of 18.5 to 40.0 kg/m^2, inclusive and weighs at least 50 kg at screening
Female participant is not pregnant and at least 1 of the following conditions apply
Not a woman of child-bearing potential (WOCBP)
WOCBP who agrees to follow the contraceptive guidance from the time of informed consent through at least 28 days after Investigational Product (IP) administration
Female participant must agree not to breastfeed starting at screening and throughout
the study period and for 28 days after IP administration
Female participant must not donate ova starting at first dose of IP and throughout the study period and for 28 days after IP administration
Male participant with female partner(s) of childbearing potential (including breastfeeding partner) must agree to use contraception throughout the treatment period and for 28 days after IP administration
Male participant must not donate sperm during the treatment period and for 28 days after IP administration
Male participant with pregnant partner(s) must agree to remain abstinent or use a condom for the duration of the pregnancy throughout the study period and for 28 days after IP administration
Participant agrees not to participate in another interventional study while participating in the present study
Participant has normal renal function as defined by estimated glomerular filtration rate (eGFR) using Modification of Diet in Renal Disease formula ≥ 90 mL/min per 1.73 m^2 or participant has varying degrees of chronic kidney disease as defined by the National Kidney Foundation and by eGFR
to < 90 mL/min per 1.73 m^2 for participants with mild renal impairment
to < 60 mL/min per 1.73 m^2 for participants with moderate renal impairment
< 30 mL/min per 1.73 m^2 and not on hemodialysis, with approximately 50 percent of participants to have eGFR ≤ 20 mL/min per 1.73 m^2 for participants with severe renal impairment
Participant has adequate venous access

Exclusion Criteria

Participant has received any investigational therapy within 28 days or 5 half-lives, whichever is longer, prior to day -1
Participant has any condition, which makes the participant unsuitable for study participation
Female participant who has been pregnant within 6 months prior to screening or breastfeeding within 3 months prior to screening
Participant has a known or suspected hypersensitivity to ASP0367 or any components of the formulation used
Participant has had previous exposure with ASP0367
Participant has used moderate or strong inducers of Cytochrome P450 (CYP) 3A within the 3 months prior to day -1
Participant has used a strong CYP3A inhibitor within 5 half lives, prior to day -1
Participant has used proton pump inhibitor within the 2 weeks prior to IP administration
Participant has used histamine 2 blockers within 24 hours prior to IP administration
Participant has any clinically significant history of allergic conditions (including drug allergies, asthma, eczema or anaphylactic reactions, but excluding untreated, asymptomatic, seasonal allergies) prior to IP administration
Participant has/had febrile illness or symptomatic, viral, bacterial (including upper respiratory infection) or fungal (noncutaneous) infection within 1 week prior to day -1
Participant has any of the liver function tests (alkaline phosphatase, alanine aminotransferase, aspartate aminotransferase and total bilirubin ≥ 1.5 × upper limit of normal (ULN) on day -1. In such a case, the assessment may be repeated once
Participant has had significant blood loss, donated ≥ 1 unit (450 mL) of whole blood or donated plasma within 7 days prior to day -1 and/or received a transfusion of any blood or blood products within 60 days
Participant is an employee of Astellas, the study related contract research organization (CRO) or the clinical unit
Participant has a positive result for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) polymerase chain reaction (PCR) test at screening
Participant has consumed grapefruit, Seville oranges, grapefruit containing products or Seville orange containing products within 72 hours prior to day -1
Participant has a history of smoking > 10 cigarettes (or equivalent amount of tobacco) per day within 3 months prior to day -1
Participant has used any drugs of abuse (amphetamines, barbiturates, benzodiazepines, cannabinoids, cocaine and/or opiates) within 3 months prior to day -1 or the participant tests positive for drugs of abuse (amphetamines, barbiturates, benzodiazepines, cannabinoids, cocaine and/or opiates) at screening or on day -1, unless the positive result is due to an approved prescription medication (for participants with renal impairment only)
For US sites: Participant has a history of consuming > 14 units for male participants or > 7 units for female participants of alcoholic beverages per week within 6 months prior to screening or has a history of alcoholism or drug/chemical/substance abuse within 2 years prior to screening (note: 1 unit = 12 ounces of beer, 4 ounces of wine, 1 ounce of spirits/hard liquor) or the participant tests positive for alcohol at screening or on day -1
For EU sites: Participant has a history of consuming > 21 units for male participants or > 14 units for female participants of alcohol per week within 3 months prior to day -1 (note: 1 unit = 10 g pure alcohol, 250 mL of beer [5 percent], 35 mL of spirits [35 percent] or 100 mL of wine [12 percent]) or the participant tests positive for alcohol at screening or on day -1
Participant has received a coronavirus disease 2019 (COVID-19) vaccine within the 2 weeks prior to IP administration or will have a COVID-19 vaccine dose before the end-of-study visit (ESV)
Participant has a positive serology test for hepatitis A virus antibodies (immunoglobulin M), hepatitis B surface antigen, hepatitis C virus antibodies or antibodies to human immunodeficiency virus type 1 and/or type 2 at screening
Participant with renal impairment will be excluded from participation in the study if any
of the following apply
Participant has a history of any clinically significant illness (other than renal
disease and conditions related to the renal disease, such as stable diabetes and
stable hypertension), medical condition or laboratory abnormality within 3 months
prior to screening
Participant has a mean pulse < 40 or > 90 bpm; mean systolic blood pressure (SBP) < 90
or > 160 mmHg; mean diastolic blood pressure (DBP) < 50 or > 100 mmHg (measurements
taken in triplicate after participant has been resting in a supine position for at
least 5 minutes; pulse will be measured automatically) on day -1. If the mean blood
pressure exceeds the limits above, 1 additional triplicate may be taken
Participant has a mean QT interval using Fridericia's correction (QTcF) of > 450 msec
(for male participants) and > 480 msec (for female participants) on day -1. If the
mean QTcF exceeds the limits above, 1 additional triplicate may be taken
Participant who has had a change in dose regimen of medically required medication(s)
in the 2 weeks prior to screening (permitted concomitant medications) and/or
participant for whom dose changes are likely to occur during the study (minor dose
changes are allowed in agreement with the sponsor) and/or participant has used
nonpermitted concomitant medication(s) in the 3 weeks prior to admission to the
clinical unit
Participant who has a renal disease secondary to malignancy
Participant who has a fluctuating or rapidly deteriorating renal function within 4
weeks prior to IP administration, as indicated by strongly varying or worsening of
clinical and/or laboratory signs of renal impairment within the screening period
Participant has a hemoglobin result of < 9 g/dL
Participant has a functioning kidney transplant
Participant has cardiac troponin I (cTnI) for a given manufacturer's assay being used
that is above the historical upper range for participants with chronic kidney injury
in the presence of cardiac symptoms or acute ECG changes suggestive of myocardial
Healthy participants with normal renal function will be excluded from participation in the
infarction or an increase in cTnI by >20% from baseline value at the 2-hour time point
at screening
study if any of the following apply
Participant has any history or evidence of any clinically significant cardiovascular
gastrointestinal, endocrinologic, hematologic, hepatic, immunologic, metabolic
urologic, pulmonary, neurologic, dermatologic, psychiatric, renal and/or other major
disease or malignancy
Participant has any clinically significant abnormality following the physical
examination, electrocardiogram (ECG) and protocol defined clinical laboratory tests at
screening or on day -1
Participant has a mean pulse < 45 or > 90 bpm; mean systolic blood pressure > 140
mmHg; mean diastolic blood pressure > 90 mmHg (measurements taken in triplicate after
participant has been resting in the supine position for at least 5 minutes; pulse will
be measured automatically) on day -1. If the mean blood pressure exceeds the limits
above, 1 additional triplicate may be taken
Participant has a mean QTcF of > 430 msec (for male participants) and > 450 msec (for
female participants) on day -1. If the mean QTcF exceeds the limits above, 1
additional triplicate ECG may be taken
Participant has used any prescribed or nonprescribed drugs (including vitamins and
natural and herbal remedies, e.g., St. John's Wort) in the 2 weeks prior to IP
administration, except for occasional use of acetaminophen (up to 2 g/day), topical
dermatological products (including corticosteroid products), hormonal contraceptives
and hormone replacement therapy
Participant has creatinine level outside normal limits on day -1. In such a case, the
assessment may be repeated once
Participant has cardiac troponin (cTnI) > Upper limit of normal (ULN) (or cardiac
troponin T [cTnT] > ULN if cTnI is not available) at screening
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