Study identifier:D9090C00009
ClinicalTrials.gov identifier:NCT06989983
EudraCT identifier:N/A
CTIS identifier:N/A
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
heart failure
Phase 1
Yes
AZD5462 film-coated tablet, [14C]AZD5462 Solution for Infusion, [14C]AZD5462 Oral Solution
Male
8
Interventional
30 Years - 65 Years
Allocation: N/A
Endpoint Classification: -
Intervention Model: Single Group Assignment
Masking: -
Primary Purpose: Treatment
Verified 01 Jun 2025 by AstraZeneca
AstraZeneca
Quotient Sciences Limited
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: AZD5462 In Period 1, participants will receive one oral dose of [14C]AZD5462. In Period 2, participants will receive one oral dose of AZD5462 and one intravenous dose of [14C]AZD5462. | - |