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NCT02419937 · ClinicalTrials.gov registry record · NA

Short-Term Application of Tocilizumab Following Myocardial Infarction

A NA study, sponsored by Keesler Air Force Base Medical Center.

Completed
Registry status
NA
Development phase
28
Enrollment target

NCT02419937: Completed NA study, sponsored by Keesler Air Force Base Medical Center.

NCT02419937 is a NA study that has completed, run by Keesler Air Force Base Medical Center. The registered enrollment target is 28 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02419937, a NA study, has completed, sponsored by Keesler Air Force Base Medical Center.

COMPLETED
Registry status
NA
Development phase
28 participants
Enrollment target

Study Summary

Introduction: Interleukin 6 (IL-6) is a cytokine that has a pro-inflammatory effect on the immune system. In acute MI IL-6 levels rapidly increase in response to ischemia and inflammation. Tocilizumab is a humanized monoclonal antibody against the interleukin-6 receptor (IL-6R). The use of tocilizumab within the first 24 hours of admission for acute MI could reduce 30 day mortality. Methods: This randomized, placebo controlled trial will assign subjects within 24 hours of admission to treatment with either 162 mg of tocilizumab subcutaneously once or placebo in addition to usual pharmacologic and interventional standard of care for acute MI (ST segment elevation MI or non-ST segment elevation MI). Outcomes: The primary outcome is difference in 30 day (plus/minus 5 days) occurrence of major adverse cardiac events (as defined later in this protocol) between placebo and Tocilizumab treated groups. Secondary outcomes to be assessed include length of hospitalization, readmission rates by day 30, CRP levels at 0 hours, 24 hours, 48 hours, and 30 days following treatment, and safety of Tocilizumab with focus on rates of known side effects.

Primary Outcome

30 day rate of major adverse cardiac events (MACE) following administration of Tocilizumab subcutaneously single dose within 24 hours of NSTEMI or STEMI as compared to administration of placebo

Interventions

  • DRUG Placebo
  • DRUG Tocilizumab

Trial Details

FieldValue
Enrollment Target 28 participants
Start Date 2015-05
Est. Completion 2017-08
Phase NA

What the finished NCT02419937 record still lists

NCT02419937 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 28 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

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

NCT02419937 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02419937 about?

NCT02419937 is a clinical study titled "Short-Term Application of Tocilizumab Following Myocardial Infarction". Introduction: Interleukin 6 (IL-6) is a cytokine that has a pro-inflammatory effect on the immune system. In acute MI IL-6 levels rapidly increase in response to ischemia and inflammation. Tocilizumab is a humanized monoclonal antibody against the interleukin-6 receptor (IL-6R). The use of tocilizum...

What is the current status of trial NCT02419937?

This trial is currently completed. It is a NA study. The enrollment target is 28 participants. The study started on 2015-05. Estimated completion is 2017-08.

What interventions are being tested in trial NCT02419937?

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

Who is sponsoring clinical trial NCT02419937?

This trial is sponsored by Keesler Air Force Base Medical Center, which has 5 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02419937's enrollment target sits among peer trials

28 1704th of 2000 higher than 293 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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 NCT02419937, the US trial registry maintained by the National Library of Medicine. NCT02419937 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.