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NCT04155645 · ClinicalTrials.gov registry record · Phase 1

To Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of AZD8233 After Multiple Dose Administration in Subjects With Dyslipidemia

A Phase 1 study, sponsored by AstraZeneca.

Completed
Registry status
Phase 1
Development phase
34
Enrollment target

NCT04155645: Completed Phase 1 study, sponsored by AstraZeneca.

NCT04155645 is a Phase 1 study that has completed, run by AstraZeneca. The registered enrollment target is 34 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (43% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04155645, a Phase 1 study, has completed, sponsored by AstraZeneca.

COMPLETED
Registry status
Phase 1
Development phase
34 participants
Enrollment target

Study Summary

This is a Phase I study to assess the safety, tolerability and pharmacokinetics (PK), and pharmacodynamics (PD) of AZD8233, following subcutaneous (SC) administration of multiple ascending doses (MAD) of AZD8233 in subjects with confirmed dyslipidemia with or without type 2 diabetes.

Primary Outcome

To assess AEs as a variable of safety and tolerability of AZD8233 following SC administration of multiple ascending doses. Serious AEs will be recorded from the time of informed consent.

Interventions

  • DRUG Placebo
  • DRUG AZD8233 subcutaneous injection

Trial Details

FieldValue
Enrollment Target 34 participants
Start Date 2019-11-21
Est. Completion 2021-06-07
Phase Phase 1
AstraZeneca

1,285 total trials

What the finished NCT04155645 record still lists

NCT04155645 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 34 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (43% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT04155645 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04155645 about?

NCT04155645 is a clinical study titled "To Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of AZD8233 After Multiple Dose Administration in Subjects With Dyslipidemia". This is a Phase I study to assess the safety, tolerability and pharmacokinetics (PK), and pharmacodynamics (PD) of AZD8233, following subcutaneous (SC) administration of multiple ascending doses (MAD) of AZD8233 in subjects with confirmed dyslipidemia with or without type 2 diabetes.

What is the current status of trial NCT04155645?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 34 participants. The study started on 2019-11-21. Estimated completion is 2021-06-07.

What interventions are being tested in trial NCT04155645?

The interventions under investigation include: Placebo (DRUG), AZD8233 subcutaneous injection (DRUG).

Who is sponsoring clinical trial NCT04155645?

This trial is sponsored by AstraZeneca, which has 1,285 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04155645's enrollment target sits among peer trials

34 1273rd of 2000 higher than 721 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT04155645, the US trial registry maintained by the National Library of Medicine. NCT04155645 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.