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A Study to Evaluate AZD7760 Safety and Pharmacokinetics in Healthy Adults (Phase I) and Adults With End-stage Kidney Disease on Hemodialysis With a Central Venous Catheter (Phase IIa)

Phase 1
Recruiting
Conditions
Staphylococcus Aureus
Interventions
Other: Placebo
Registration Number
NCT06749457
Lead Sponsor
AstraZeneca
Brief Summary

The purpose of this study is to evaluate the safety and pharmacokinetics (PK) of AZD7760 when given as an intravenous infusion to healthy participants (Phase I) or participants with end-stage kidney disease receiving hemodialysis through a central venous catheter (Phase IIa).

Detailed Description

In the Phase I portion of the study, participants will be randomized into one of 3 cohorts to receive one of 3 dosages of AZD7760 or placebo as a single intravenous infusion.

Study details include:

* A 28-day Screening Period.

* A Dosing Period of 3 days in which a single intravenous infusion will be given on Day 1.

* A Follow-up Period of 12 months from the time of administration of the study intervention.

In the Phase IIa portion of the study, participants will be randomized into one of 3 study groups to receive either AZD7760 or placebo as 2 intravenous infusions given 3 months apart.

Study details include:

* A 28-day Screening Period.

* A Dosing Period in which 2 intravenous infusions will be given 3 months apart (Day 1 and Day 91).

* A Follow-up Period of 12 months after the last administration of the study intervention on Day 91.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
231
Inclusion Criteria

Phase I:

  • Participant must be 18 to 55 years of age (inclusive), at the time of signing the informed consent.
  • Body weight ≥ 45 kilograms (kg) and ≤ 110 kg and Body Mass Index (BMI) within the range ≥ 18.0 to ≤ 30.0 kilograms per square meter (kg/m2) (inclusive) at screening.
  • Healthy participants with no clinically significant concomitant diseases or medications (except for those specifically permitted by the protocol) according to medical history, physical examination, screening safety laboratory tests, and screening parameters, as perthe judgement of the investigator.

Phase IIa:

  • Participant must be ≥ 18 years of age at the time of signing the informed consent.

  • Participants who meet all of the following disease status requirements:

    1. Diagnosed with End-stage kidney disease (ESKD).
    2. Requiring hemodialysis through a tunneled central venous catheter as the primary vascular access for hemodialysis.
    3. Receiving hemodialysis for treatment of ESKD for at least 90 days before randomization.
    4. At least 3 previous dialysis sessions using current dialyzer.
    5. Receiving adequate hemodialysis based on a single-pool Kt/V measurement > 1.2 within the last 30 days.
    6. No new medications have been added to the participant's regimen in the last 2 weeks prior to dosing. 'New medication' is defined as any medication that has not been prescribed or used by the participant previously (including formulation changes). Medication previously prescribed or used by the participant with dose adjustments is allowed and not considered as new medication for the purpose of this study.
    7. Not taking long-term systemic antibiotics with activity against S aureus.
Exclusion Criteria

Phase I:

  • Known hypersensitivity to any component of the study intervention
  • Previous hypersensitivity, infusion-related reaction, or severe adverse reaction following administration of monoclonal antibodies (mAbs).
  • Clinically significant bleeding disorder (eg, factor deficiency, coagulopathy, or platelet disorder), or prior history of significant bleeding or bruising following intramuscular injections or venipuncture.
  • Aspartate Aminotransferase (AST) or alanine Aminotransferase (ALT) above 1.5 × upper limit of normal (ULN) at screening. Testing may be repeated once at the investigator's discretion.
  • Estimated glomerular filtration rate < 90 mL/min/1.73 m2 calculated using the Chronic Kidney Disease Epidemiology Collaboration equation at screening.
  • Hemoglobin or platelet count below the lower limit of normal at screening. Testing may be repeated once at the investigator's discretion.
  • White blood cell counts outside normal reference ranges unless judged by the investigator to be out of range given the known variation in white blood cell count reference interval by ethnicity. Testing may be repeated once at the investigator's discretion.
  • History of malignancy other than treated non-melanoma skin cancers or locally treated cervical cancer in the previous 5 years.
  • Any laboratory value in the screening panel that, in the opinion of the investigator, is clinically significant or might confound analysis of study results. Testing may be repeated once at the investigator's discretion.
  • Any clinically significant abnormalities on 12-lead electrocardiogram (ECG) at screening, as judged by the investigator.
  • Acute (time-limited) illness, including fever ≥ 38 °C (100.4 °F), one day prior to or on day of planned dosing; participants excluded for transient acute illness may be dosed if illness resolves within the 28-day Screening Period or may be rescreened once.
  • Known or suspected congenital or acquired immunodeficiency, or receipt of immunosuppressive therapy, including any course of glucocorticoid therapy exceeding 2 weeks of prednisone or equivalent at a dose of 20 mg daily or every other day within 6 months prior to screening.
  • Any condition that has the potential to increase clearance of the study intervention (eg, protein loss conditions such as severe enteropathies, or plasmapheresis).
  • Blood drawn in excess of a total of 450 milliliters (mL) (1 unit) for any reason within 2 months prior to screening.
  • Absence of suitable veins for blood sampling and administration of study intervention.
  • Any other condition that would compromise safety of the participants.
  • Any condition that, in the opinion of the investigator, might interfere with evaluation of the study intervention or interpretation of participant safety or study results.

Phase IIa:

  • Known hypersensitivity to any component of the study intervention.
  • History of allergic disease or reactions likely to be exacerbated by any component of the study intervention as listed in dose formulation section.
  • Previous hypersensitivity, infusion-related reaction, or severe adverse reaction following administration of mAbs.
  • Hemoglobin < 9 g/dL at screening considered by the investigator to be due to acute condition(s). Testing may be repeated once at the investigator's discretion.
  • Serum albumin of < 3 g/dL at screening considered by the investigator to be due to acute condition(s). Testing may be repeated once at the investigator's discretion.
  • Myocardial infarction, acute coronary syndrome, stroke, seizure, or a thrombotic/thromboembolic event (eg, deep vein thrombosis or pulmonary embolism, but excluding vascular access thrombosis) within 90 days prior to randomization.
  • Known S aureus infection within 90 days of study entry.
  • Known acute viral or bacterial infection or symptoms/signs consistent with such an infection within the 21 days prior to infusion or study intervention. Mild intercurrent viral illness with a temperature of 38.1 °C (100.6 °F) or less does not require exclusion, if in the judgement of the investigator this illness will not interfere with the evaluation of the mAb.
  • Participants with malignancy undergoing chemotherapy.
  • Scheduled date for living donor kidney transplant.
  • Plans to switch to peritoneal dialysis within the primary endpoint time period (181 days).
  • Participants with a scheduled calendar date for transition to arteriovenous graft or arteriovenous graft in place and maturing.
  • Participants with a scheduled calendar date for transition to arteriovenous fistula, or arteriovenous fistula in place and maturing, with anticipated use of fistula within 90 days.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Phase I: Cohort 1 (AZD7760 Dose A and Placebo)AZD7760Participants will receive a single dose of AZD7760 Dose A or matching placebo intravenously on Day 1.
Phase IIa: Study Group 1 (AZD7760 Dose D and Placebo)AZD7760Participants will receive Dose D AZD7760 on Day 1 and placebo on Day 91.
Phase IIa: Study Group 2 (AZD7760 Dose E)AZD7760Participants will receive Dose E AZD7760 on Day 1 and Day 91.
Phase I: Cohort 1 (AZD7760 Dose A and Placebo)PlaceboParticipants will receive a single dose of AZD7760 Dose A or matching placebo intravenously on Day 1.
Phase I: Cohort 2 (AZD7760 Dose B and Placebo)AZD7760Participants will receive a single dose of AZD7760 Dose B or matching placebo intravenously on Day 1.
Phase I: Cohort 2 (AZD7760 Dose B and Placebo)PlaceboParticipants will receive a single dose of AZD7760 Dose B or matching placebo intravenously on Day 1.
Phase I: Cohort 3 (AZD7760 Dose C and Placebo)AZD7760Participants will receive a single dose of AZD7760 Dose C or matching placebo intravenously on Day 1.
Phase I: Cohort 3 (AZD7760 Dose C and Placebo)PlaceboParticipants will receive a single dose of AZD7760 Dose C or matching placebo intravenously on Day 1.
Phase IIa: Study Group 1 (AZD7760 Dose D and Placebo)PlaceboParticipants will receive Dose D AZD7760 on Day 1 and placebo on Day 91.
Phase IIa: Study Group 3 (Placebo)PlaceboParticipants will receive placebo on Day 1 and on Day 91.
Primary Outcome Measures
NameTimeMethod
Phase I: Occurence of adverse events (AEs)Day 1 to Day 181

To evaluate the safety of AZD7760 administered as a single intravenous (IV) Dose A, B, or C.

Phase I: Occurence of medically-attended adverse events (MAAEs), serious adverse events (SAEs), and adverse events of special interest (AESIs)Day 1 to Day 361

To evaluate the safety of AZD7760 administered as a single IV Dose A, B, or C.

Phase IIa: Occurrence of AEs, MAAEs, SAEs, and AESIsDay 1 to Day 181

To evaluate the safety of AZD7760 compared with placebo as:

* A single IV dose (at Day 1) of Dose D followed by placebo (at Day 91)

* 2 IV doses (at Day 1 and Day 91) of Dose E

Secondary Outcome Measures
NameTimeMethod
Phase IIa: Occurrence of MAAEs, SAEs, and AESIsDay 1 to Day 451

To evaluate the safety to Day 451 of AZD7760 administered as:

* A single IV dose (at Day 1) of Dose D followed by placebo (at Day 91)

* 2 IV doses (at Day 1 and Day 91) of Dose E

Phase I: Area under the plasma concentration-curve from zero to the last quantifiable concentration (AUClast)Day 1 to Day 361

To characterize the PK of AZD7760 in serum.

Phase I: Maximum observed plasma (peak) drug concentration (Cmax)Day 1 to Day 361

To characterize the pharmacokinetics (PK) of AZD7760 in serum.

Phase I: Time to reach peak or maximum observed concentration following drug administration (tmax)Day 1 to Day 361

To characterize the PK of AZD7760 in serum.

Phase I: Half-life associated with terminal slope (λz) of a semi-logarithmic concentration-time curve (t1/2λz)Day 1 to Day 361

To characterize the PK of AZD7760 in serum.

Phase I: Area under plasma concentration-time curve from zero extrapolated to infinity (AUCinf)Day 1 to Day 361

To characterize the PK of AZD7760 in serum.

Phase I: Apparent volume of distribution at steady state (Vss)Day 1 to Day 361

To characterize the PK of AZD7760 in serum.

Phase I: Apparent volume of distribution at the terminal phase (Vz)Day 1 to Day 361

To characterize the PK of AZD7760 in serum.

Phase I: Incidence of ADADay 1 to Day 361

To evaluate ADA responses to AZD7760 in serum.

Phase IIa: CmaxDay 181 to Day 451

To characterize the serum PK profiles of AZD7760 administered as:

* A single IV dose (at Day 1) of Dose D followed by placebo (at Day 91)

* 2 IV doses (at Day 1 and Day 91) of Dose E

Phase IIa: tmaxDay 181 to Day 451

To characterize the serum PK profiles of AZD7760 administered as:

* A single IV dose (at Day 1) of Dose D followed by placebo (at Day 91)

* 2 IV doses (at Day 1 and Day 91) of Dose E

Phase IIa: t1/2λzDay 181 to Day 451

To characterize the serum PK profiles of AZD7760 administered as:

* A single IV dose (at Day 1) of Dose D followed by placebo (at Day 91)

* 2 IV doses (at Day 1 and Day 91) of Dose E

Phase IIa: AUClastDay 181 to Day 451

To characterize the serum PK profiles of AZD7760 administered as:

* A single IV dose (at Day 1) of Dose D followed by placebo (at Day 91)

* 2 IV doses (at Day 1 and Day 91) of Dose E

Phase IIa: AUCinfDay 181 to Day 451

To characterize the serum PK profiles of AZD7760 administered as:

* A single IV dose (at Day 1) of Dose D followed by placebo (at Day 91)

* 2 IV doses (at Day 1 and Day 91) of Dose E

Phase IIa: VssDay 181 to Day 451

To characterize the serum PK profiles of AZD7760 administered as:

* A single IV dose (at Day 1) of Dose D followed by placebo (at Day 91)

* 2 IV doses (at Day 1 and Day 91) of Dose E

Phase IIa: VzDay 181 to Day 451

To characterize the serum PK profiles of AZD7760 administered as:

* A single IV dose (at Day 1) of Dose D followed by placebo (at Day 91)

* 2 IV doses (at Day 1 and Day 91) of Dose E

Phase IIa: Incidence of anti-drug antibodies (ADAs) to AZD7760 in serumDay 181 to Day 451

To evaluate ADA responses to AZD7760 administered as:

* A single IV dose (at Day 1) of Dose D followed by placebo (at Day 91)

* 2 IV doses (at Day 1 and Day 91) of Dose E

Phase IIa: Occurrence of AEsDay 1 to Day 181

To evaluate the safety to Day 181 of AZD7760 administered as:

* A single IV dose (at Day 1) of Dose D followed by placebo (at Day 91)

* 2 IV doses (at Day 1 and Day 91) of Dose E

Trial Locations

Locations (1)

Research Site

🇺🇸

San Antonio, Texas, United States

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