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NCT03370887 · ClinicalTrials.gov registry record · Phase 2

AZD8601 Study in CABG Patients

A Phase 2 study of Heart Failure, sponsored by AstraZeneca.

Completed
Registry status
Phase 2
Development phase
11
Enrollment target
10
Study locations

NCT03370887 is a Phase 2 study of Heart Failure that has completed, run by AstraZeneca. The registered enrollment target is 11 participants, below the 2,049-participant average among 397 other Heart Failure trials with a reported enrollment target (99% lower). The trial reports 10 study locations across 2 states.

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The verdict

NCT03370887, a Phase 2 study of Heart Failure, has completed, sponsored by AstraZeneca.

COMPLETED
Registry status
Phase 2
Development phase
11 participants
Enrollment target
10
Study locations

Study Summary

This is a randomized, double-blind, placebo-controlled, sequential design, multicentre study in patients with moderately impaired systolic function undergoing CABG surgery. Twenty four (24) patients scheduled for elective bypass surgery will be randomized (up to approximately 33 patients if replacements are needed). The objective is to investigate safety and tolerability of AZD8601 following epicardial injection in patients undergoing Coronary Artery Bypass Grafting (CABG) surgery with moderately impaired systolic function. At Visit 3 patients will receive either AZD8601 or placebo as epicardial injections and will then be followed up at 14 days (telephone visit) and 1, 3 and 6 months (on-site) post-surgery.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG AZD8601

Study Locations (10)

Other

  • Research Site - Kuopio
  • Research Site - Tampere
  • Research Site - Turku
  • Research Site - München
  • Research Site - München
  • Research Site - Amsterdam
  • Research Site - Groningen
  • Research Site - Gothenburg
  • Research Site - Uppsala

Connecticut

  • Research Site - New Haven

Trial Details

FieldValue
Enrollment Target 11 participants
Start Date 2018-02-05
Est. Completion 2021-06-30
Phase Phase 2

Sponsor

AstraZeneca

1,285 total trials

What the Registry Record Tells You About NCT03370887

The ClinicalTrials.gov registry entry for NCT03370887 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 11 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 2,049-participant average among 397 other Heart Failure trials with a reported enrollment target (99% lower). The listed sponsor is AstraZeneca, which has 1,285 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Heart Failure appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT03370887 reports 10 study locations spanning 2 distinct geographic areas - top geographies include Other, Connecticut.

Frequently Asked Questions

What is clinical trial NCT03370887 about?

NCT03370887 is a clinical study titled "AZD8601 Study in CABG Patients". This is a randomized, double-blind, placebo-controlled, sequential design, multicentre study in patients with moderately impaired systolic function undergoing CABG surgery. Twenty four (24) patients scheduled for elective bypass surgery will be randomized (up to approximately 33 patients if replacem...

What is the current status of trial NCT03370887?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 11 participants. The study started on 2018-02-05. Estimated completion is 2021-06-30.

What conditions does trial NCT03370887 study?

This clinical trial studies the following conditions: Heart Failure.

What interventions are being tested in trial NCT03370887?

The interventions under investigation include: Placebo (DRUG), AZD8601 (DRUG).

Who is sponsoring clinical trial NCT03370887?

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

Where is trial NCT03370887 being conducted?

This trial has 10 study locations across Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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