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

Completed · Phase 2 · Has a placebo group

Conditions studied: Coronavirus Disease 2019 (COVID-19)

In brief

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)

Key facts

Study ID

NCT04409509

Run by

CSL Behring

People needed

124

Starts

2020-07-01

Expected to finish

2021-01-12

Last updated by the study team

2022-01-24

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age ≥ 18 years
• Positive for severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection as determined using a molecular diagnostic test (reverse transcription polymerase chain reaction [RT-PCR] or equivalent) approved by regulatory authorities (including Food and Drug Administration or Brazilian Health Regulatory Agency) or allowed under an emergency use authorization within 14 days before Screening. If a false negative result is suspected, the SARS-CoV-2 test may be repeated within the Screening Period.
• Chest CT scan or X ray results confirming interstitial pneumonia
• Severe COVID 19 disease as evidenced by ≥ 1 of the following criteria at Screening including within 24 hours before Screening:
• Respiratory frequency > 30 breaths per minute
• SpO2 ≤ 93% on room air
• Ratio of partial pressure of arterial oxygen to fraction of inspired oxygen (PaO2/FiO2) < 300
• Ratio of Arterial oxygen saturation to fraction of inspired oxygen (SaO2/FiO2 ratio) < 218 (if PaO2/FiO2 ratio is not available)
• Radiographic lung infiltrates > 50%

You may not qualify if…

• Currently enrolled, planning to enroll, or participated, within the last 30 days, in a clinical study requiring administration of an IP, including expanded access or compassionate use with the only exception being administration of convalescent plasma. Administration of IP is permitted only if an emergency use authorization has been granted (eg, remdesivir). Additionally, off label use of approved drugs (eg, anti IL 6/anti IL 6R) is also permitted.
• Pregnant or breastfeeding (female subjects)
• Intubated and require mechanical ventilation (including ECMO) at the time of randomization
• In the opinion of the investigator, the subject is expected to be intubated in the first 24 hours after IMP administration
• Has a Do-Not-Intubate (DNI) or Do-Not-Resuscitate (DNR) order
• In the opinion of the investigator, not expected to survive for > 48 hours after admission
• Presence of any of the following comorbid conditions prior to randomization and prior to SARS CoV 2 infection:
• Severe heart failure (New York Heart Association Class IV)
• End stage renal disease (Stage ≥ 4) or need for renal replacement therapy
• Biopsy confirmed cirrhosis, portal hypertension, or hepatic encephalopathy
• Malignancy (Stage IV)
• Chronic lung disease requiring the use of oxygen at home
• Active tuberculosis disease
• Active bleeding or a current clinically significant coagulopathy (eg, international normalized ratio [INR] > 1.5) or clinically significant risk for bleeding (eg, recent intracranial hemorrhage or bleeding peptic ulcer within the last 4 weeks)
• History of venous thrombosis, myocardial infarction or cerebrovascular event within 3 months, or a prothrombotic disorder (eg, antithrombin III, protein C or protein S deficiency)
• Known or suspected Grade 3 or 4 infusion-related reaction or hypersensitivity (per Common Terminology Criteria for Adverse Events [CTCAE]) to monoclonal antibody therapy, or hypersensitivity to the IMP or any excipients of the IMP
• Currently receiving a therapy not permitted during the study.
• Female subject of childbearing potential or fertile male subject either not using or not willing to use an acceptable method of contraception to avoid pregnancy during the study and for 90 days after receipt of the last dose of IMP
• Any clinical or laboratory abnormality or other underlying conditions (eg, psychological disorders, substance abuse) that would render the subject unsuitable for participation in the study, in the opinion of the investigator

Where it is running

• Nova Clinical Research, LLC — Bradenton, Florida, United States
• Theia Clinical Research, LLC — St. Petersburg, Florida, United States
• MercyOne North Iowa Medical Center — Mason City, Iowa, United States
• Northeast Iowa Medical Education Foundation — Waterloo, Iowa, United States
• Lahey Hospital and Medical Center — Burlington, Massachusetts, United States
• University of Mississippi Medical Center — Jackson, Mississippi, United States
• Holy Name Hospital — Teaneck, New Jersey, United States
• Inspira Health Center Vineland — Vineland, New Jersey, United States
• Sisters of Charity Hospital/ St. Joseph's Campus — Buffalo, New York, United States
• Carolina Institute for Clinical Research — Fayetteville, North Carolina, United States
• Monument Health Clinical Research — Rapid City, South Dakota, United States
• PharmaTex Research — Amarillo, Texas, United States
• UT Health Science Center, McGovern Medical School — Houston, Texas, United States
• Inova Alexandria Hospital — Alexandria, Virginia, United States

Full record on ClinicalTrials.gov

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