A Phase Ib Study of AZD5462 on Top of Dapagliflozin in Participants With Heart Failure and Moderate Renal Impairment
- Sponsor
- AstraZeneca
- Study ID
- NCT06639087
- Phase
- PHASE1
- Status
- Terminated
Conditions
- Heart Failure
- Renal Impairment
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 85 Years
- Healthy Volunteers
- Not accepted
Interventions
- AZD5462 — DRUGParticipants will receive AZD5462 on top of dapagliflozin once daily.
- Dapagliflozin — DRUGParticipants will receive dapagliflozin once daily with AZD5462 or placebo.
- Placebo — OTHERParticipants will receive placebo on top of dapagliflozin once daily.
Study Details
A study to investigate the effects and safety of AZD5462 on top of dapagliflozin in participants with heart failure and moderate renal impairment.
Key Dates
- Start date
- Sep 27, 2024
- Status verified
- Sep 2025
- Primary completion
- May 29, 2025
- Completion
- May 29, 2025
Study Design
- Enrollment
- 8 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Active Comparator: AZD5462 + dapagliflozinParticipants will receive AZD5462 on top of dapagliflozin once daily.
- Placebo Comparator: Placebo + dapagliflozinParticipants will receive placebo on top of dapagliflozin once daily.
Primary Outcome Measure
Change in sodium excretion [ Time Frame: From Baseline to Day 1 ]
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