AzTrials
AzTrials

Hepatic ImpairmentPhase 1NCT06388616

Study to Investigate the Effect of Hepatic Impairment on the Pharmacokinetics, Safety, and Tolerability of Balcinrenone

A Phase 1 study testing Balcinrenone in people with Hepatic Impairment, run by AstraZeneca at 3 sites in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

This study will evaluate the pharmacokinetics (PK), safety, and tolerability of a single oral dose of balcinrenone in patients with mild and moderate hepatic impairment in comparison to a matched healthy control group. Read more about this study

Who is it for?
Ages 18 to 79 yearsHealthy volunteers can take part
Conditions the study is for
Hepatic Impairment
What is being tested?
Balcinrenone
Type of treatment
Pill or oral medicine
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
3 sitesUnited States
Study dates
2 May 2024to 5 Sep 2024
Phase
Phase 1
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 79 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Participant must be 18 to 79 years of age, inclusive, at the time of signing the informed consent.
  • For participant with hepatic impairment:
  • Participant must have a diagnosis of chronic (≥ 6 months) and stable hepatic impairment Child Pugh Class A or B (eg, no clinically significant change in signs, symptoms, or laboratory parameters of hepatic disease status within 30 days prior to study screening, as determined by the investigator at screening and Day -1).
  • Supporting documents confirming the participant's hepatic impairment must be available; participant self-report is not acceptable; the participant must be classified by the investigator as CP Class A or B at screening.
  • Participants must be stable on a concomitant medication and/or treatment regimen (defined as not starting a new treatment/medication[s] or a change in the dosage or frequency of the concomitant medication[s] within 2 weeks prior to screening). Minor changes in dosage can be accepted at the discretion of the investigator.
  • For participant with normal hepatic function:
Show all 20Show fewer
  • Participant must be medically healthy with no clinically significant medical history, physical examination, laboratory profiles, vital signs, or 12-lead ECGs, as deemed by the investigator at screening and Day -1.
  • Body weight ≥ 50 kg; BMI within the range of 18.0 to 42.0 kg/m2 (inclusive) as measured at screening.
  • Sex: male and female.
  • Females must not be lactating and must not have a positive pregnancy test at screening and at Day -1.
  • Women of childbearing potential (defined as female participants who are neither permanently sterilised [hysterectomy, bilateral oophorectomy, or bilateral salpingectomy] nor postmenopausal) must use a highly effective method of contraception (described below).
  • A highly effective method of contraception is defined as one that can achieve a failure rate of less than 1% per year when used consistently and correctly. Women of childbearing potential who are sexually active with a non-sterilised male partner must agree to use one highly effective method of birth control, as defined below, from enrolment throughout the study and until at least 4 weeks after study intervention.
  • Highly effective methods of contraception include: sexual abstinence (periodic abstinence [eg, calendar, ovulation, symptothermal, post-ovulation methods], declaration of abstinence for the duration of exposure to IMP, and withdrawal [coitus interruptus], spermicides only, and lactational amenorrhoea method are not acceptable methods of contraception), a vasectomised partner, bilateral tubal occlusion, combined (oestrogen- and progestogen-containing) hormonal contraception associated with inhibition of ovulation (oral, intravaginal, transdermal), progestogen-only hormonal contraception associated with inhibition of ovulation (oral, injectable, implantable), intrauterine device, intrauterine hormone-releasing system.
  • Women of nonchildbearing potential (defined as female participants who are permanently surgically sterilised [hysterectomy, bilateral oophorectomy, or bilateral salpingectomy] or postmenopausal).
  • Women will be considered postmenopausal if they have been amenorrhoeic for 12 months prior to the planned date of study intervention without an alternative medical cause. The following age-specific requirements apply:
  • Women < 55 years old would be considered postmenopausal if they have been amenorrhoeic for 12 months or more following cessation of exogenous hormonal treatment and FSH levels in the postmenopausal range.
  • Women ≥ 55 years old would be considered postmenopausal if they have been amenorrhoeic for 12 months or more following cessation of all exogenous hormonal treatment.
  • Postmenopausal status for participants with hepatic impairment based on FSH levels may be at the discretion of the investigator.
  • Capable of giving signed informed consent as described in Appendix A which includes compliance with the requirements and restrictions listed in the ICF and in this protocol.
  • Provision of signed and dated written ICF prior to any mandatory study-specific procedures, sampling, and analyses.

Who cannot join

  • Participant has eGFR < 60 mL/minute/1.73 m2 as calculated by CKD-EPI.
  • History of severe allergy/hypersensitivity or ongoing clinically important allergy/hypersensitivity, as judged by the investigator at screening or Day -1, or history of hypersensitivity to drugs with a similar chemical structure or class to balcinrenone.
  • History of long QT syndrome or any clinically significant abnormalities on 12-lead ECG at screening or Day -1, as judged by the investigator, including but not limited to any of the following:
  • Any significant arrhythmia.
  • Conduction abnormalities (eg, Wolff Parkinson White syndrome, second degree AV block; at the discretion of the investigator).
  • Prolonged QTcF > 450 ms for participants with normal hepatic function; > 480 ms for participants with mild or moderate hepatic impairment.
Show all 67Show fewer
  • Clinically significant PR (PQ) interval shortening (< 120 ms) or prolongation (> 240 ms); intermittent second or third degree AV block, or AV dissociation.
  • Complete bundle branch block and/or QRS duration > 120 ms.
  • Any of the following signs or confirmation of COVID-19 infection at screening or Day -1:
  • Participant has a positive SARS-CoV-2 test result within 2 weeks prior to screening, at screening, or on Day -1.
  • Clinical signs and symptoms consistent with COVID-19 (eg, fever, dry cough, dyspnoea, sore throat, fatigue) within 2 weeks prior to screening or Day -1.
  • Positive test for HIV at screening.
  • Positive results at screening for hepatitis B surface antigen, hepatitis B core antibody or hepatitis C virus. Participants with impaired hepatic function with positive total hepatitis B core antibody or positive hepatitis C result may be included if a follow-up hepatitis B virus DNA test or follow-up hepatitis C virus RNA test is negative.
  • History or presence of clinically significant thyroid disease, in the opinion of the investigator. Participants with clinically significant TSH levels outside normal limits at screening will not be enrolled. Participants on stable thyroid replacement therapy are not excluded.
  • History or presence of clinically significant or unstable medical or psychiatric condition or disease in the opinion of the investigator.
  • Participant is mentally or legally incapacitated or has significant emotional problems at the time of the screening visit or Day -1 or expected during the conduct of the study.
  • History of any major surgical procedure within 30 days prior to study intervention.
  • Any clinically or surgically significant condition that may affect balcinrenone absorption and/or excretion in the opinion of the investigator, including gastric restrictions and bariatric surgery (eg, gastric bypass). Uncomplicated appendectomy and hernia repair will be allowed. Uncomplicated cholecystectomy is allowed at the discretion of the investigator.
  • Judgment by the investigator that the participant should not participate in the study if they have any ongoing or recent (ie, during the screening period) minor medical complaints that may interfere with the interpretation of study data or if they are considered unlikely to comply with study procedures, restrictions, and requirements.
  • Use of any medication defined as prohibited medication (see Appendix E) within 2 weeks prior to study intervention or longer if the medication has a long half-life.
  • Unable to refrain from the following for 10 hours prior to and 10 hours after study intervention: Phosphate binders (eg, aluminium hydroxide and calcium carbonanate).
  • Acid reducing agents (eg, ranitidine/nizatidine or proton pump inhibitors). Cholestyramine/colestipol. MRA agents (eg, spironolactone, eplerenone, finerenone).
  • Has received another new chemical entity (defined as a compound which has not been approved for marketing) within 30 days of study intervention in this study or, if known, 5 half-lives from last dose in the previous study to study intervention in this study, whichever is longest.
  • Previous enrolment in the present study. Note: participants consented and screened, but not receiving study intervention in this study or a previous Phase I study, are not excluded.
  • Participant smokes more than 10 cigarettes (ie, 1/2 pack) per day or equivalent (eg, e-vapor cigarette, pipe, cigar, chewing tobacco, nicotine patch, nicotine gum) and is unable to comply with the nicotine restrictions (Section 5.3.2) during the study.
  • Positive screen for drugs of abuse (unless participant has hepatic impairment and positive screen is due to medication[s] prescribed by physician) and/or alcohol test at screening or Day -1.
  • Receipt of blood products within 2 months prior to Day -1, plasma or platelets donation within 1 month prior to Day -1, or any blood donation/blood loss > 500 mL within 3 months prior to Day -1.
  • Involvement of any AstraZeneca or clinical unit employee or their close relatives.
  • Vulnerable participants, eg, kept in detention, protected adults under guardianship, trusteeship, or committed to an institution by governmental or juridical order.
  • Judgment by the investigator that the participant should not participate in the study if the participant is unlikely to comply with study procedures, restrictions, and requirements.
  • Participants with hepatic impairment are excluded from the study if any of the following criteria apply:
  • Esophageal banding within 3 months prior to Day -1 or required treatment for gastrointestinal bleeding within 6 months prior to Day -1.
  • Ascites requiring paracentesis and albumin infusion at 4-week intervals or less.
  • History of paracentesis within 30 days prior to screening.
  • Fluctuating or rapidly deteriorating hepatic function, as indicated by strongly varying or worsening of clinical and/or laboratory signs of hepatic impairment within the screening period.
  • In the opinion of the investigator, any evidence of additional severe or uncontrolled systemic disease (eg, currently unstable or uncompensated renal, cardiovascular, or respiratory disease) or laboratory finding that makes it unsafe for the participant to participate in the study.
  • Presence of a hepatocellular carcinoma or acute liver disease caused by an infection or drug toxicity.
  • Hepatic impairment due to non-liver disease (eg, right HF).
  • Biliary obstruction or other causes of hepatic impairment not related to parenchymal disorder and/or disease of the liver.
  • Clinically relevant hepatic encephalopathy (Grade 2 or more) at screening or Day -1.
  • Has required new medication for hepatic encephalopathy within the 3 months prior to Day -1.
  • Platelet count < 35 × 109/L and/or neutrophil count < 1.2 × 109/L and/or haemoglobin < 85 g/L.
  • Current functioning organ transplant or anticipated to receive organ transplant within 2 months of screening or Day -1.
  • Participant has had a porto-systemic shunt (including transjugular intrahepatic portosystemic shunts).
  • History of drug abuse within 1 year prior to screening.
  • History of alcohol abuse within 3 months prior to screening and/or consumes > 21 units per week for males and > 14 units per week for females. One unit of alcohol equals 12 oz (360 mL) beer, 1½ oz (45 mL) liquor, or 5 oz (150 mL) wine.
  • Supine systolic BP > 160 or <90 mmHg, and diastolic BP > 95 or < 40 mmHg at screening or Day -1. One repeat is allowed.
  • Supine pulse rate < 50 bpm or > 99 bpm at screening or Day -1. One repeat is allowed.
  • Cardiac bradyarrhythmia or tachyarrhythmia requiring treatment (atrial fibrillation/flutter with optimal control of ventricular rate is not excluded) at screening or Day -1.
  • Blood dyscrasias with increased risk of bleeding including idiopathic thrombocytopenic purpura and thrombotic thrombocytopenic purpura or symptoms of increased risk of bleeding (frequent bleeding gums or nose bleeds) at screening or Day -1.
  • History of unstable diabetes mellitus as evidenced by hemoglobin A1c ≥ 9% at screening.
  • Participants with normal hepatic function are excluded from the study if any of the following criteria apply:
  • History of any clinically important disease or disorder, which, in the opinion of the investigator, may either put the participant at risk because of participation in the study, or influence the results or the participant's ability to participate in the study.
  • History or presence of gastrointestinal, hepatic, or renal disease or any other condition known to interfere with absorption, distribution, metabolism, or excretion of drugs.
  • Any clinically important illness, medical/surgical procedure, or trauma within 4 weeks of dose administration.
  • Any laboratory values with the following deviations at screening or Day -1
  • (1 confirmatory repeat is allowed):
  • ALT and/or AST > 1.2 × ULN.
  • White blood cell count and/or platelet count < lower limit of normal; haemoglobin < 11.0 g/dL for females or < 12.0 g/dL for males.
  • Activated partial thrombin time and prothrombin time (or INR) > 1.2 × ULN.
  • Bilirubin > 1.5 × ULN (or known Gilbert's syndrome).
  • Changes in any current medication (initiation, dose change, or cessation), that may impact the study readouts (as judged by the investigator) within 2 weeks prior to screening and until study intervention. This criterion does not apply to medication prescribed for occasional use.
  • History or presence of hepatic disease or evidence of other known forms of known chronic liver disease, eg, alcoholic liver disease, hepatitis B, hepatitis C, primary biliary cirrhosis, primary sclerotic cirrhosis, autoimmune hepatitis, Wilson disease, iron overload, alpha-1-antitrypsin deficiency, drug-induced liver injury, known or suspected hepatocellular carcinoma.
  • History of drug abuse within 2 years prior to screening.
  • History of alcohol abuse within 2 years prior to screening and/or consumes > 21 units per week for males and > 14 units per week for females. One unit of alcohol equals 12 oz (360 mL) beer, 1½ oz (45 mL) liquor, or 5 oz (150 mL) wine.
  • Supine systolic BP > 150 or < 90 mmHg, and diastolic BP > 95 or < 50 mmHg at screening or Day -1. One repeat is allowed.
  • Supine pulse rate < 45 bpm or > 100 bpm at screening or Day -1. One repeat is allowed.

Trial locations and contacts

3 sites in 1 country.

United States3 sites

  • Research Site

    Hialeah, Florida, 33014

  • Research Site

    Orlando, Florida, 32809

  • Research Site

    San Antonio, Texas, 78215

Other trials in United States

About this study

Official title: A Phase I, Single-Dose, Non-Randomised, Open-Label, Parallel-Group Study to Investigate the Effect of Hepatic Impairment on the Pharmacokinetics, Safety, and Tolerability of Balcinrenone

This study will evaluate the pharmacokinetics (PK), safety, and tolerability of a single oral dose of balcinrenone in patients with mild and moderate hepatic impairment in comparison to a matched healthy control group.

Read the detailed description

This is an open-label, non-randomised, multicentre, parallel-group, single-dose study to examine the PK, safety, and tolerability of balcinrenone 50 mg administered orally to male and female participants with mild or moderate hepatic impairment compared with control participants with normal hepatic function. Eight participants with mild impairment and 8 participants with moderate impairment per CP classification and 8 to 12 participants with normal hepatic function matched on a group level regarding age, BMI, and sex to the impaired groups are planned for study intervention. All participants will receive a single dose of balcinrenone 50 mg on Day 1 following an overnight fast. Study intervention will be administered orally with approximately 240 mL of water.

Child-Pugh scoring will be used to determine the level of hepatic impairment. Participants will be enrolled into the following groups based on their CP classification score as determined at screening:

  • Group 1: Participants with mild hepatic impairment (CP Class A, score of 5 or 6).
  • Group 2: Participants with moderate hepatic impairment (CP Class B, score of 7 to 9).
  • Group 3: Participants with normal hepatic function matched on a group level regarding age, BMI, and sex to the impaired groups.
Being tested
Balcinrenone
Keywords
Hepatic Impairment, Healthy participants, Balcinrenone, Pharmacokinetics, Safety

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • BalcinrenoneDrug

    Also called AZD9977

    50 mg, Immediate release capsule to be taken orally.

Study groups in NCT06388616
Study groupRoleWhat they receive
Group 1ExperimentalSubjects with Mild Impairment will receive a single oral dose of balcinrenone under fasted conditions.
Receives: Drug: Balcinrenone
Group 2ExperimentalSubjects with Moderate Impairment will receive a single oral dose of balcinrenone under fasted conditions.
Receives: Drug: Balcinrenone
Group 3ExperimentalHealthy participants will receive a single oral dose of balcinrenone under fasted conditions.
Receives: Drug: Balcinrenone

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Area under plasma concentration-time curve from time zero to the last measurable concentration (AUClast)

    To compare the PK of a single oral dose of balcinrenone in participants with mild and moderate hepatic impairment to those with normal hepatic function

    Measured: Day 1 to Day 5

  2. Area under plasma concentration-time curve from zero to infinity (AUCinf)

    To compare the PK of a single oral dose of balcinrenone in participants with mild and moderate hepatic impairment to those with normal hepatic function

    Measured: Day 1 to Day 5

  3. Maximum observed plasma concentration (Cmax)

    To compare the PK of a single oral dose of balcinrenone in participants with mild and moderate hepatic impairment to those with normal hepatic function

    Measured: Day 1 to Day 5

Secondary outcomes (3)

  1. AEs and SAEs up to the follow-up telephone call (Day 10 [± 3 days])

    To assess the safety and tolerability of a single oral dose of balcinrenone in participants with mild and moderate hepatic impairment and those with normal hepatic function

    Measured: Screening (day -28 to day -2) to day 10

  2. Number of participants with abnormal Vital signs, abnormal ECGs, and abnormal physical examination findings

    To assess the safety and tolerability of a single oral dose of balcinrenone in participants with mild and moderate hepatic impairment and those with normal hepatic function

    Measured: Screening (day -28 to day -2) to day 4

  3. Number of participants with abnormal laboratory tests results

    To assess the safety and tolerability of a single oral dose of balcinrenone in participants with mild and moderate hepatic impairment and those with normal hepatic function

    Measured: Screening (day -28 to day -2) to day 4

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted29 Apr 2024
  2. Study start2 May 2024
  3. Primary completion5 Sep 2024
  4. Study completion5 Sep 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 1
Primary purpose
Treatment
Allocation
Non-randomised
Intervention model
Parallel groups
Model description
Three cohorts (two hepatic impairment cohorts and controls with normal hepatic function) will be enrolled into this study. All subjects will receive the study intervention: * Cohort 1 will enroll 8 participants with mild hepatic impairment * Cohort 2 will enroll 8 participants with moderate hepatic impairment * Cohort 3 will enroll 8-12 healthy participants matched on a group level regarding age, BMI and sex
Masking
None (open label)
Enrolment
30 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06388616
Sponsor's protocol ID
D6402C00013
Status last verified
Nov 2024
First submitted
16 Apr 2024
Last updated
12 Nov 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
Yes: Qualified researchers can request access to anonymized individual patient-level data from AstraZeneca group of companies sponsored clinical trials via the request portal. All requests will be evaluated as per the AZ disclosure commitment: https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure. Yes, indicates that AZ are accepting requests for IPD, but this does not mean all requests will be shared.

Questions about this trial

What is this clinical trial studying?

A Phase 1 study testing Balcinrenone in people with Hepatic Impairment, run by AstraZeneca at 3 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 20 inclusion and 67 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 12 Nov 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 3 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Area under plasma concentration-time curve from time zero to the last measurable concentration (AUClast) (time frame: Day 1 to Day 5). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06388616.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 Nov 2024.

AzTrials uses cookies for analytics and advertising. You can accept or reject them; the site works either way. Privacy Policy.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in