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A Phase 1b, Double-blind, Placebo-controlled, Randomised Trial Investigating the Effect of AZD3427 on Renal Perfusion in HFrEF Patients With Renal Impairment Using Positron Emission Tomography (PET)

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-513143-82-00
Acronym
D8330C00004
Enrollment
12
Registered
2024-08-28
Start date
2024-10-15
Completion date
2025-08-21
Last updated
2025-02-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart failure with reduced ejection fraction, Renal impairment

Brief summary

The volumetric fraction (%) of the renal cortex with increased perfusion from baseline to Day 8, compared to placebo, as measured by quantitative parametric mapping using PET.

Detailed description

Safety and tolerability will be evaluated in terms of AEs, vital signs, clinical laboratory assessments, and ECG.

Interventions

Sponsors

AstraZeneca AB
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
The volumetric fraction (%) of the renal cortex with increased perfusion from baseline to Day 8, compared to placebo, as measured by quantitative parametric mapping using PET.

Secondary

MeasureTime frame
Safety and tolerability will be evaluated in terms of AEs, vital signs, clinical laboratory assessments, and ECG.

Countries

Sweden

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026