drugset / Trial / NCT04482621

Decitabine for Coronavirus (COVID-19) Pneumonia- Acute Respiratory Distress Syndrome (ARDS) Treatment: DART Trial

NCT04482621

Phase 2 Suspended 33 enrolled Johns Hopkins University
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a a randomized double blind placebo controlled Phase 2 trial with a 12 patient lead-in to evaluate safety, prior to full enrollment to an additional 28 patients (for a total of 40 patients) to assess efficacy of decitabine in the treatment of critically ill patients with COVID-ARDS. The patients will be randomized in a 1:1 ratio to receive standard of care plus Decitabine or standard of care plus saline based placebo. The primary objective is to determine safety and efficacy of decitabine for COVID-19 ARDS based on clinical improvement on a 6-point clinical scale.

Timeline

Start
2020-09-14
Primary completion
2026-07
Completion
2026-12

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Decitabine Small molecule 10 mg/m2 Intravenous

Indications