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Completed Phase 2 Interventional Results available

Treatment With CSL312 in Adults With Coronavirus Disease 2019 (COVID-19)

ClinicalTrials.gov ID: NCT04409509

Public ClinicalTrials.gov record NCT04409509. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 27, 2026, 10:55 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Multicenter, Double Blind, Randomized, Placebo-Controlled Study to Evaluate CSL312 in Coronavirus Disease 2019 (COVID 19)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a prospective, phase 2, multicenter, randomized, double blind, placebo controlled, parallel group study to assess the safety and efficacy of CSL312 administered intravenously, in combination with standard of care (SOC) treatment, in patients with Coronavirus disease 2019 (COVID 19)

Study identification

NCT ID
NCT04409509
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
CSL Behring
Industry
Enrollment
124 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 1, 2020 (Actual)
Primary completion
Jan 12, 2021 (Actual)
Completion
Jan 12, 2021 (Actual)
Last update posted
Jan 24, 2022

2020 – 2021

United States locations

U.S. sites
14
U.S. states
10
U.S. cities
14
Facility City State ZIP Site status
Nova Clinical Research, LLC Bradenton Florida 34209 —
Theia Clinical Research, LLC St. Petersburg Florida 33707 —
MercyOne North Iowa Medical Center Mason City Iowa 50401 —
Northeast Iowa Medical Education Foundation Waterloo Iowa 50702 —
Lahey Hospital and Medical Center Burlington Massachusetts 01805 —
University of Mississippi Medical Center Jackson Mississippi 39216 —
Holy Name Hospital Teaneck New Jersey 07666 —
Inspira Health Center Vineland Vineland New Jersey 08360 —
Sisters of Charity Hospital/ St. Joseph's Campus Buffalo New York 14225 —
Carolina Institute for Clinical Research Fayetteville North Carolina 28304 —
Monument Health Clinical Research Rapid City South Dakota 57701 —
PharmaTex Research Amarillo Texas 79109 —
UT Health Science Center, McGovern Medical School Houston Texas 77030 —
Inova Alexandria Hospital Alexandria Virginia 22304 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04409509, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 24, 2022 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04409509 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →