SOLIRIS® (Eculizumab) Treatment of Participants With COVID-19

NCT04355494 · Status: NO_LONGER_AVAILABLE · Type: EXPANDED_ACCESS

Last updated 2021-03-09

No results posted yet for this study

Summary

This protocol provides access to eculizumab treatment for participants with severe COVID-19.

Conditions

  • COVID-19
  • Pneumonia, Viral
  • Acute Lung Injury/Acute Respiratory Distress Syndrome (ARDS)

Interventions

BIOLOGICAL

eculizumab

Eculizumab at doses of 900-1200 mg will be administered intravenously (up to 7 doses)

Sponsors & Collaborators

  • Alexion Pharmaceuticals, Inc.

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Countries

  • United States
  • France

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04355494 on ClinicalTrials.gov