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A Phase IIb, Multicenter, Randomized, Parallel-group, Double- blind, Placebo-controlled, Dose-ranging Study to Evaluate the Efficacy, Safety, and Tolerability of AZD0780 in Participants with Dyslipidemia

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2023-506197-12-00
Acronym
PURSUIT
Enrollment
209
Registered
2024-01-16
Start date
2024-02-07
Completion date
2024-09-25
Last updated
2024-04-12

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

Conditions

Dyslipidemia Dyslipidemias are alterations to the plasma lipid profile associated often with clinical condition. A common form of dyslipidemia is Hypercholesterolemia due to high level of LDL-cholesterol, such as Ischemic Heart Disease and Ischemic Stroke. CVD is a leading cause of global mortality and a contributor to disability., which is a major risk factor for Cardiovascular Disease (CVD)

Brief summary

Percent change from baseline of Low-Density Lipoprotein cholesterol (LDL-C) at Week 12

Detailed description

Percent change from baseline of Low-Density Lipoprotein cholesterol (LDL-C) at Week 12, AZD0780 plasma concentrations summarized by sampling timepoint, Percent change from baseline at Week 12 in, total cholesterol, high-density lipoprotein cholesterol (HDL-C), triglycerides, non-high-density lipoprotein cholesterol (Non-HDL-C), very low-density lipoprotein cholesterol (VLDL-C), apolipoprotein A-1 (ApoA1), apolipoprotein B-100 (ApoB), lipoprotein (a) (Lp(a)), remnant cholesterol, and high-sensitivity C-reactive protein (hsCRP)., Percent change from baseline at Week 12 in, total cholesterol, high-density lipoprotein cholesterol (HDL-C), triglycerides, non-high-density lipoprotein cholesterol (Non-HDL-C), very low-density lipoprotein cholesterol (VLDL-C), apolipoprotein A-1 (ApoA1), apolipoprotein B-100 (ApoB), lipoprotein (a) (Lp(a)), remnant cholesterol, and high-sensitivity C-reactive protein (hsCRP)., Safety and tolerability will be assessed in terms of adverse events, vital signs, electrocardiogram (ECG), and clinical laboratory evaluations

Interventions

Sponsors

Astrazeneca AB
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Percent change from baseline of Low-Density Lipoprotein cholesterol (LDL-C) at Week 12

Secondary

MeasureTime frame
Percent change from baseline of Low-Density Lipoprotein cholesterol (LDL-C) at Week 12, AZD0780 plasma concentrations summarized by sampling timepoint, Percent change from baseline at Week 12 in, total cholesterol, high-density lipoprotein cholesterol (HDL-C), triglycerides, non-high-density lipoprotein cholesterol (Non-HDL-C), very low-density lipoprotein cholesterol (VLDL-C), apolipoprotein A-1 (ApoA1), apolipoprotein B-100 (ApoB), lipoprotein (a) (Lp(a)), remnant cholesterol, and high-sensitivity C-reactive protein (hsCRP)., Percent change from baseline at Week 12 in, total cholesterol, high-density lipoprotein cholesterol (HDL-C), triglycerides, non-high-density lipoprotein cholesterol (Non-HDL-C), very low-density lipoprotein cholesterol (VLDL-C), apolipoprotein A-1 (ApoA1), apolipoprotein B-100 (ApoB), lipoprotein (a) (Lp(a)), remnant cholesterol, and high-sensitivity C-reactive protein (hsCRP)., Safety and tolerability will be assessed in terms of adverse events, vital signs, el

Countries

Czechia, Denmark, Hungary, Slovakia, Spain

Outcome results

None listed

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