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OpenTrials
Completed

NCT Number: NCT01069783

Study of A3309 in Patients With Dyslipidemia

The purpose of this trial is to determine the efficacy and safety of A3309 administered to patients with dyslipidemia (high cholesterol levels).

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

BCRC

Linköping, Sweden

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients meet protocol specified criteria for dyslipidemia and has successfully completed study requirements with no clinically relevant findings

Exclusion criteria

  • Medical history or medical condition that would not make the patient a good candidate for the study or would limit the patient´s capability to complete the study

Treatment and study plan

A3309

Drug

A3309 in two different dosage levels

Placebo

Drug

Placebo comparator once daily for the duration of the trial

Primary outcomes

  1. Change from baseline in low-density lipoprotein (LDL) cholesterol

    Time frame: eight weeks

Sponsors and collaborators

Lead sponsor

Albireo

Industry

Registry information

Official study title

A Phase IIa, Double-blind, Randomised, Placebo-controlled, Dose-finding Efficacy and Safety Study of A3309 in Patients With Dyslipidemia

Important dates

Study start
2010
Primary completion
2010
Study completion
2010
First posted
Feb 17, 2010
Registry last updated
Mar 7, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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