Anti-CD14 Treatment With IC14 in Hospitalized ARDS Patients

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorImplicit Bioscience

About this trial

Hospitalized patients with ARDS will be randomized to intravenous treatment with a monoclonal antibody against CD14, called IC14, or placebo. They will be followed for 28 days.

The primary outcome is the day 4 oxygenation index assessed as a continuous measure.

Eligibility criteria

Qualifiers

Adult patients (18+) on mechanical ventilations with acute respiratory distress syndrome (ARDS) by Berlin Criteria (≤48 hours)

P:F ratio < 300

Positive end-expiratory pressure (PEEP) ≥5 cm H2O

Bilateral opacities on chest x-ray or chest computerized tomography (CT)-- not fully explained by effusions, lobar/lung collapse, or nodules

Disqualifiers

Significant pre-existing organ dysfunction prior to hospitalization

Lung: Currently receiving home oxygen therapy as documented in medical record

Heart: Pre-existing congestive heart failure defined as an ejection fraction <20% as documented in the medical record

Renal: End-stage renal disease requiring renal replacement therapy or estimated glomerular filtration rate (eGFR) <30 mL/min.

Trial design

Treatments tested in this trial

  • Atibuclimab
  • Placebo

Treatment groups

56 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Implicit Bioscience

Lead sponsor

University of Washington

Collaborator