🔎 Trials Near Me

Home › Post-COVID Conditions (Long COVID) › NCT04652115

Defibrotide for the Treatment of Severe COVID-19

RecruitingPhase 2Healthy volunteers welcome

A Single-Arm Safety and Feasibility Study of Defibrotide for the Treatment of Severe COVID-19

Who can join

Ages 18 to 100 · All sexes · Healthy volunteers welcome

Full eligibility criteria
Inclusion Criteria:

1. Age ≥18 years.
2. Active COVID-19 infection confirmed by positive SARS-CoV-2 PCR.
3. Radiographic evidence of bilateral pulmonary infiltrates.
4. A life expectancy of at least 24 hours.
5. Score of 4-7 on the WHO ordinal scale.
6. Prophylactic dose anticoagulation is allowed for enrollment into cohort 1. Therapeutic dose anticoagulation for active thrombosis, ECMO, and/or continuous renal replacement therapy (CRRT) is allowed for enrollment into cohort 2 if there is no evidence of bleeding after at least 24 hours of anticoagulation.
7. Patient or surrogate able to provide informed consent

Exclusion Criteria:

1. Clinically significant acute bleeding.
2. Concomitant use of thrombolytic therapy (e.g. t-PA).
3. Hemodynamic instability, defined as a requirement for \>1 vasopressor agent for enrollment into cohort 1, and a requirement for \>2 vasopressor agents for enrollment into cohort 2
4. Known allergy or hypersensitivity to DF.
5. Pregnant or lactating.

About the study

The goal of this study is to evaluate the safety and feasibility of defibrotide in COVID-19 pneumonia.

What is being tested

Sponsor: Brigham and Women's Hospital · Participants: 42 · Started: Jan 1, 2021

Contact the study team

Official record on ClinicalTrials.gov — NCT04652115

Locations in the U.S.

MassachusettsBrigham and Women's Hospital, Boston

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.