A Study to Assess the Safety, Tolerability, and Pharmacokinetics of a Single Ascending Dose of AZD0292 in Healthy Japanese Participants

AstraZeneca

Status and phase: Enrolling; Phase 1

Conditions: Healthy Participants

Treatments: Drug: Placebo; Drug: AZD0292

Study type: Interventional

Funder types: Industry

Identifiers

NCT07222254

D7700C00004

Details and patient eligibility

About

The purpose of the study is to evaluate the safety, tolerability and pharmacokinetics (PK) of single ascending doses of AZD0292 administered via intravenous (IV) infusion in healthy Japanese participants.

Full description

This is a Phase I, randomized, double-blind, placebo-controlled, single ascending dose study in healthy Japanese participants to investigate 2 dose levels of AZD0292. Participants will be randomized to receive either AZD0292 or placebo, proceeding with sentinel cohorts.

The study will comprise:

• A Screening Period of maximum 28 days.
• A Treatment Period during which participants will be resident at the site from the day before study intervention administration (Day -1) until at least 24 h post-EOI with study intervention; and discharged on Day 2.
• A Follow-up Period from Day 3 to Day 16.
• An extended Follow-up Period from Day 17 to Day 161.

Enrollment: 18 estimated patients

Sex: All

Ages: 18 to 60 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Healthy Japanese participants with suitable veins for cannulation or repeated venipuncture.
• Women of childbearing potential (WOCBP) must have a negative pregnancy test and must not be lactating.
• Participants must agree to use an approved method of highly effective contraception as defined in the protocol.
• Have a body mass index (BMI) between 18 and 32 kg/m2 inclusive and weigh at least 45 kg at screening.

Exclusion criteria

• History of any clinically important disease or disorder which 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.
• History of malignancy, other than treated non-melanoma skin cancers or locally-treated cervical cancer, in the previous 5 years.
• Any clinically important illness, chronic infections or individuals who are at increased risk of infection.
• History of acquired or inherited immunodeficiency disorders.
• History of severe coronavirus disease 2019 (COVID-19) infection requiring hospitalization within the last 12 months or clinical history compatible with ongoing long COVID-19.
• Current smokers or those who have smoked or used nicotine products within the previous 6 months prior to screening.
• History of alcohol or drug abuse within the past 2 years.
• History of severe allergy/hypersensitivity or ongoing clinically important allergy/hypersensitivity, as judged by the PI or history of hypersensitivity to drugs with a similar chemical structure or class to AZD0292 and excipients contained in AZD0292.
• Known hypersensitivity to antihistamines.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Sequential Assignment

Masking: Quadruple Blind

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18 participants in 2 patient groups

AZD0292 Dose Level 1

Experimental group

Description:

Participants will receive AZD0292 (dose level 1) or matching placebo on Day 1.

Treatment:

Drug: AZD0292

Drug: Placebo

AZD0292 Dose Level 2

Experimental group

Description:

Participants will receive AZD0292 (dose level 2) or matching placebo on Day 1.

Treatment:

Drug: AZD0292

Drug: Placebo