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Completed Phase 2 Interventional Results available

A Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamic Effects of MEDI5884 in Adults With Stable Coronary Heart Disease

ClinicalTrials.gov ID: NCT03351738

Public ClinicalTrials.gov record NCT03351738. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 30, 2026, 2:27 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2a Randomized, Double-blind, Placebo-controlled, Parallel-designed Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamic Effects of MEDI5884 in Subjects With Stable Coronary Heart Disease

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

A Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamic Effects of MEDI5884 in Adults With Stable Coronary Heart Disease.

Study identification

NCT ID
NCT03351738
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
MedImmune LLC
Industry
Enrollment
133 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
45 Years to 80 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 13, 2017 (Actual)
Primary completion
Nov 9, 2018 (Actual)
Completion
Nov 9, 2018 (Actual)
Last update posted
Mar 23, 2020

2017 – 2018

United States locations

U.S. sites
23
U.S. states
14
U.S. cities
23
Facility City State ZIP Site status
Research Site Anniston Alabama 36207 —
Research Site Huntsville Alabama 35801 —
Research Site El Cajon California 92020 —
Research Site Lincoln California 95648 —
Research Site Northridge California 91325 —
Research Site Waterbury Connecticut 06708 —
Research Site Fleming Island Florida 32003 —
Research Site Jacksonville Florida 32216 —
Research Site Pembroke Pines Florida 33024 —
Research Site Port Orange Florida 32127 —
Research Site Savannah Georgia 31406 —
Research Site Evanston Illinois 60201 —
Research Site Indianapolis Indiana 46260 —
Research Site Louisville Kentucky 40213 —
Research Site Fargo North Dakota 58103 —
Research Site Cincinnati Ohio 45219 —
Research Site Marion Ohio 43302 —
Research Site Stow Ohio 44224 —
Research Site Oklahoma City Oklahoma 73134 —
Research Site Rapid City South Dakota 57701 —
Research Site Kingsport Tennessee 37660 —
Research Site McAllen Texas 78503 —
Research Site San Antonio Texas 78228 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03351738, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 23, 2020 · Synced Oct 30, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03351738 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →