Study identifier:CIN-107-117
ClinicalTrials.gov identifier:NCT05961384
EudraCT identifier:N/A
CTIS identifier:N/A
A Phase 1, Open-Label Study Of The Absorption, Metabolism, And Excretion Of [14C]-baxdrostat Following A Single Oral Dose In Healthy Male Subjects
hypertension
Phase 1
Yes
baxdrostat
Male
8
Interventional
18 Years - 55 Years
Allocation: N/A
Endpoint Classification: -
Intervention Model: Single Group Assignment
Masking: -
Primary Purpose: Treatment
Verified 01 Aug 2023 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: 10 mg [14C]-bexdrostat single oral dose of 10 mg baxdrostat containing 100 μCi of [14C] baxdrostat | - |