A Study Designed to Assess the Mass Balance Recovery, Absorption, Metabolism, Excretion of [14C]AZD5462 and the Absolute Bioavailability of AZD5462

Study identifier:D9090C00009

ClinicalTrials.gov identifier:NCT06989983

EudraCT identifier:N/A

CTIS identifier:N/A

Study Complete

Official Title

An Open-Label, Two-Period Study Designed to Assess the Mass Balance Recovery, Absorption, Metabolism, Excretion of [14C]AZD5462 and the Absolute Bioavailability of AZD5462 in Healthy Male Participants

Medical condition

heart failure

Phase

Phase 1

Healthy volunteers

Yes

Study drug

AZD5462 film-coated tablet, [14C]AZD5462 Solution for Infusion, [14C]AZD5462 Oral Solution

Sex

Male

Actual Enrollment

8

Study type

Interventional

Age

30 Years - 65 Years

Date

Study Start Date: 20 May 2025
Primary Completion Date: 25 Jun 2025
Study Completion Date: 25 Jun 2025

Study design

Allocation: N/A
Endpoint Classification: -
Intervention Model: Single Group Assignment
Masking: -
Primary Purpose: Treatment

Verification:

Verified 01 Jun 2025 by AstraZeneca

Sponsors

AstraZeneca

Collaborators

Quotient Sciences Limited

Inclusion and exclusion criteria