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Avdoralimab an Anti-C5aR Antibody, in Patients With COVID-19 Severe Pneumonia ( FORCE )

Phase 2
Completed
Conditions
COVID
Interventions
Other: Placebo
Biological: avdoralimab
Registration Number
NCT04371367
Lead Sponsor
Assistance Publique Hopitaux De Marseille
Brief Summary

The primary objective of this trial is to improve the proportion of COVID-19 patients with severe pneumonia who no longer need to be hospitalized, and to reduce the need for and duration of mechanical ventilation in patients with COVID-19 pneumonia complicated by acute respiratory distress syndrome (ARDS).

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
208
Inclusion Criteria
  • COVID-19 severe pneumonia patients need for oxygen therapy ≥ 5 l/min or high-flow oxygen therapy
  • COVID-19 related Acute Respiratory Distress Syndrome (ARDS) requiring mechanical ventilation
Exclusion Criteria
  • Pregnant woman
  • Uncontrolled sepsis of bacterial or fungal origin

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
PlaceboPlacebointravenous administration of Placebo
avdoralimabavdoralimabBiological/Vaccine: avdoralimab intravenous administration of avdoralimab Other Names: • IPH5401
Primary Outcome Measures
NameTimeMethod
Number of ventilator-free days at Day 28 (VFD28)day 28

Number of days without mechanical ventilation at Day 28 for COVID-19 related Acute Respiratory Distress Syndrome (ARDS) Patients hospitalized in ICU

Clinical improvement using WHO ordinal scaleday 28

improvement of WHO ordinal scale

Secondary Outcome Measures
NameTimeMethod
Number of participants with treatment-related adverse eventsday 28

Trial Locations

Locations (1)

Assistance Publique Hôpitaux de Marseille

🇫🇷

Marseille, France

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