Viewing Study NCT06357520



Ignite Creation Date: 2024-05-06 @ 8:22 PM
Last Modification Date: 2024-10-26 @ 3:26 PM
Study NCT ID: NCT06357520
Status: COMPLETED
Last Update Posted: 2024-07-03
First Post: 2024-04-05

Brief Title: A Study to Investigate the Pharmacokinetics of Baxdrostat When Given Alone and in Combination With Itraconazole in Healthy Participants
Sponsor: AstraZeneca
Organization: AstraZeneca

Study Overview

Official Title: An Open-label Fixed Sequence Study in Healthy Participants to Assess the Pharmacokinetics of Baxdrostat When Administered Alone and in Combination With Itraconazole
Status: COMPLETED
Status Verified Date: 2024-06
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The main purpose of this study is to assess the effect of itraconazole on the pharmacokinetic PK of baxdrostat
Detailed Description: This study will be an open-label 3-period fixed sequence study conducted at a single Clinical Unit

The study will comprise of

A Screening Period of maximum 28 days
Period 1 Period 1 will start from Day -1 to Day 6 followed by pharmacokinetic PK sampling of baxdrostat Baxdrostat administration on Day 1 to Day 6
Period 2 Period 2 will start from Day 6 after the last PK sample in period 1 to Day 8 Itraconazole administration on Days 6 to 8 twice a day BID on Day 6 and once daily QD on Days 7 and 8
Period 3 Period 3 will start from Day 9 to Day 17 Baxdrostat administration on Day 9 and itraconazole administration on Days 9 to 16 QD
A Final Follow-up Visit at 7 to 14 days after the last baxdrostat PK sample in Period 3

All participants will receive 2 single doses of baxdrostat and 12 doses of itraconazole under fed conditions

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None