Pharmacokinetics of Cotadutide in Participants With Hepatic Impairment

A Phase I, Parallel-group, Multi-center, Open-label, Investigation of the Pharmacokinetics, Safety and Tolerability of a Single Subcutaneous Injection of Cotadutide in Participants With Mild, Moderate or Severe Hepatic Impairment Compared to Participants With Normal Hepatic Function

This study will assess the pharmacokinetics (PK), safety, and tolerability of a single subcutaneous injection of cotadutide in participants with mild, moderate or severe hepatic impairment compared to participants with normal hepatic function.

Study Overview

• Status: Terminated
• Conditions: Hepatic Impairment
• Intervention / Treatment: Combination product: Cotadutide

Detailed Description

This study will consist of four cohorts (Cohort 1, Cohort 2, Cohort 3, and Cohort 4).

Participants will be assigned to each of the cohorts as per Child-Pugh classification:

• Cohort 1: Mild hepatic impairment (Child-Pugh A), cotadutide 50 μg
• Cohort 2: Moderate hepatic impairment (Child-Pugh B), cotadutide 50 μg
• Cohort 3: Severe hepatic impairment (Child-Pugh C), cotadutide 50 μg
• Cohort 4: Normal hepatic function, cotadutide 50 μg

• Study Type: Interventional
• Enrollment (Actual): 24
• Phase: Phase 1

Contacts and Locations

Study Locations

• United States
  • Florida
    • Hialeah, Florida, United States, 33014
      • Research Site
  • Texas
    • San Antonio, Texas, United States, 78229
      • Research Site
    • San Antonio, Texas, United States, 78215
      • Research Site

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 85 years (Adult, Older Adult)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Participant must be ≥ 18 to ≤ 85 years of age at the time of signing the Informed Consent Form (ICF).
• Body mass index ≥ 18 kg/m2 to < 40 kg/m2.
• Female participants of childbearing potential must use at least one highly effective form of birth control.
• Capable of giving signed informed consent.

Participants with hepatic impairment only

- Diagnosis of chronic (≥ 6 months) and stable hepatic impairment (eg, no clinically significant change in signs, symptoms, or laboratory parameters of hepatic disease status within 30 days prior to study Screening).

Exclusion Criteria:

All participants

• History of severe allergy/hypersensitivity or ongoing clinically important allergy/hypersensitivity, or history of hypersensitivity to drugs with a similar chemical structure or class to cotadutide.

• Any clinically important abnormalities in rhythm, conduction or morphology of the 12-lead resting electrocardiogram (ECG) and any clinically important abnormalities in the 12-lead ECG as considered by the Investigator that may interfere with the interpretation of QT interval corrected for heart rate using Fridericia's formula (QTcF), including abnormal ST-T-wave morphology, or left ventricular hypertrophy

  1. Prolonged QTcF > 470 ms or family history of long QT syndrome.
  2. PR (PQ) interval shortening < 120 ms.
  3. PR (PQ) interval prolongation (> 220 ms) intermittent or permanent second or third degree atrioventricular (AV) block, or AV dissociation.
  4. Persistent or intermittent complete bundle branch block, or intraventricular conduction delay with QRS > 119 ms.
• Any evidence of additional severe or uncontrolled systemic disease or laboratory finding that makes it unsafe for the participant to participate in the study.
• Impaired renal function, defined as estimated glomerular filtration rate (eGFR) < 30 mL/minute/1.73 m2 at Screening.
• Any positive result on Screening for serum hepatitis B surface antigen, anti-Core HBV antibody, hepatitis C antibody, or human immunodeficiency virus (HIV).
• Any sign and confirmation of coronavirus disease 2019 (COVID19) infection:
• Participants with concurrent or previous use of a glucagon-like peptide-1 (GLP1) receptor agonist.
• Use of prohibited prescribed or nonprescribed medication during the 2 weeks prior to the first administration of Investigational Medicinal Product (IMP) or longer if the medication has a long half-life.
• History of neoplastic disease within 5 years prior to Screening, except for adequately treated basal cell, squamous cell skin cancer, or in situ cervical cancer.
• Presence of hepatocellular carcinoma or acute liver disease caused by an infection or drug toxicity.

Participants with hepatic impairment only

• Severe portal hypertension or surgical porto-systemic shunts.
• Biliary obstruction or other causes of hepatic impairment not related to parenchymal disorder and/or disease of the liver.
• Clinically relevant hepatic encephalopathy.
• Severe ascites defined as ascites requiring paracentesis and albumin at 4-week intervals or less.
• Fluctuating or rapidly deteriorating hepatic function, as indicated by strongly varying or worsening of clinical and/or laboratory signs of hepatic impairment within the 28-day Screening period.
• Post liver transplantation.
• Platelet count < 50 × 109/L and/or neutrophil count < 1.2 × 109/L and/or hemoglobin < 8.5 g/dL or INR >2.3.

Participants with normal hepatic function only

• History or presence of hepatic disease or evidence of other known forms of known chronic liver disease.
• History or presence of gastrointestinal, hepatic, or renal disease, or any other condition known to interfere with absorption, distribution, metabolism, or excretion of drugs.
• Urinary albumin-to-creatinine ratio > 3 mg/μmol.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Non-Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

4

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Cohort 1; Participants in each cohort will receive Dose A cotadutide subcutaneously.	Combination product: Cotadutide; Participants will receive cotadutide subcutaneously.
Experimental: Cohort 2; Participants in each cohort will receive Dose A cotadutide subcutaneously.	Combination product: Cotadutide; Participants will receive cotadutide subcutaneously.
Experimental: Cohort 3; Participants in each cohort will receive Dose A cotadutide subcutaneously.	Combination product: Cotadutide; Participants will receive cotadutide subcutaneously.
Experimental: Cohort 4; Participants in each cohort will receive Dose A cotadutide subcutaneously.	Combination product: Cotadutide; Participants will receive cotadutide subcutaneously.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Maximum observed plasma (peak) drug concentration [Cmax]	The Cmax of a single dose of cotadutide in participants with mild, moderate, or severe hepatic impairment compared to those with normal hepatic function will be assessed.	Day 1 to Day 3
Area under plasma concentration time curve from zero to infinity (AUCinf)	The AUCinf of a single dose of cotadutide in participants with mild, moderate, or severe hepatic impairment compared to those with normal hepatic function will be assessed.	Day 1 to Day 3
Area under the plasma concentration-curve from time zero to last quantifiable concentration (AUClast)	The AUClast of a single dose of cotadutide in participants with mild, moderate, or severe hepatic impairment compared to those with normal hepatic function will be assessed.	Day 1 to Day 3
Time to reach peak or maximum observed concentration or response following drug administration (tmax)	The tmax of a single dose of cotadutide in participants with mild, moderate, or severe hepatic impairment compared to those with normal hepatic function will be assessed.	Day 1 to Day 3
Terminal half-life (t½λz)	The t½λz of a single dose of cotadutide in participants with mild, moderate, or severe hepatic impairment compared to those with normal hepatic function will be assessed.	Day 1 to Day 3
Apparent total body clearance (CL/F)	The CL/F of a single dose of cotadutide in participants with mild, moderate, or severe hepatic impairment compared to those with normal hepatic function will be assessed.	Day 1 to Day 3
Apparent volume of distribution based on the terminal phase (Vz/F)	The Vz/F of a single dose of cotadutide in participants with mild, moderate, or severe hepatic impairment compared to those with normal hepatic function will be assessed.	Day 1 to Day 3

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Number of participants with Adverse Events (AEs)	The safety, and tolerability of a single dose of cotadutide in participants with hepatic impairment will be assessed.	From time of first dose to the final follow-up visit (Day 29)
Incidence of ADAs (anti-drug antibodies)	The safety, and tolerability of a single dose of cotadutide in participants with hepatic impairment will be assessed.	From time of first dose to the final follow-up visit (Day 29)

Collaborators and Investigators

• Sponsor: AstraZeneca
• Collaborators: Parexel

Study record dates

Study Major Dates

• Study Start (Actual): September 6, 2022
• Primary Completion (Actual): February 27, 2023
• Study Completion (Actual): February 27, 2023

Study Registration Dates

• First Submitted: August 24, 2022
• First Submitted That Met QC Criteria: August 24, 2022
• First Posted (Actual): August 26, 2022

Study Record Updates

• Last Update Posted (Actual): March 21, 2023
• Last Update Submitted That Met QC Criteria: March 17, 2023
• Last Verified: March 1, 2023

More Information

Terms related to this study

• Keywords: Hepatic impairment; Cotadutide
• Additional Relevant MeSH Terms: Digestive System Diseases; Liver Diseases
• Other Study ID Numbers: D5671C00008

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: YES

IPD Plan Description

Qualified researchers can request access to anonymized individual patient-level data from AstraZeneca group of companies sponsored clinical trials via the request portal. All request 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.

• IPD Sharing Time Frame: AstraZeneca will meet or exceed data availability as per the commitments made to the EFPIA Pharma Data Sharing Principles. For details of our timelines, please rerefer to our disclosure commitment at https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure.
• IPD Sharing Access Criteria: When a request has been approved AstraZeneca will provide access to the de-identified individual patient-level data in an approved sponsored tool. Signed Data Sharing Agreement (non-negotiable contract for data accessors) must be in place before accessing requested information. Additionally, all users will need to accept the terms and conditions of the SAS MSE to gain access. For additional details, please review the Disclosure Statements at https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure.

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: Yes
• Studies a U.S. FDA-regulated device product: No