CSL324 in COVID-19

NCT ID: NCT04519424

Last Updated: 2020-10-14

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: PHASE2
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-09-30
• Study Completion Date: 2021-05-31

Brief Summary

This is a phase 2, prospective, multicenter, randomized, double blind, placebo controlled, parallel group study to evaluate the safety and efficacy of intravenous (IV) administration of CSL324, administered in combination with SOC treatment, in subjects with COVID 19.

For the purposes of this study, standard of care (SOC) may include any written or established treatment protocol followed at the study site for the treatment of severe COVID-19 or its complications, including off-label use of marketed pharmaceutical products and / or products with emergency use authorization granted for the treatment of COVID-19 (ie, not yet marketed) (eg, remdesivir).

Conditions

Coronavirus Disease 2019 (COVID-19)

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

CSL324

CSL324 administered intravenously

Group Type: EXPERIMENTAL

CSL324

Intervention Type: BIOLOGICAL

Recombinant anti-granulocyte colony-stimulating factor (G-CSF) receptor monoclonal antibody

Placebo

Normal saline administered intravenously

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Normal saline (0.9% sodium chloride)

Interventions

CSL324

Recombinant anti-granulocyte colony-stimulating factor (G-CSF) receptor monoclonal antibody

Intervention Type: BIOLOGICAL

Placebo

Normal saline (0.9% sodium chloride)

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Age ≥ 18 years at the time informed consent is obtained
• Positive for SARS-CoV-2 infection determined by a diagnostic test approved by the Food and Drug Administration (FDA) or allowed under an emergency use authorization
• Chest computed tomography (CT) scan or X ray results confirming interstitial pneumonia
• Meets ≥ 1 of the following criteria (subjects improving while on respiratory support still qualify):

• Respiratory rate > 30 breaths per minute
• Peripheral (capillary) oxygen saturation (SpO2) ≤ 93% on room air
• Partial pressure of oxygen in arterial blood (PaO2) to fraction of inspired oxygen (FiO2) ratio (PaO2 / FiO2) < 300
• SpO2 / FiO2 ratio < 218 (if PaO2 / FiO2 ratio is not available)
• Radiographic lung infiltrates > 50%

Exclusion Criteria

• Currently enrolled, planning to enroll, or participated, within the last 30 days, in a clinical study requiring administration of an investigational product (ie, not yet marketed), including expanded access or compassionate use

• Exceptions:

• Administration of investigational product with emergency use authorization granted for treatment of COVID 19 (eg, remdesivir) is permitted
• Convalescent plasma as part of approved special access programs such as expanded access, emergency IND, or compassionate use is permitted
• Pregnant or breastfeeding (female subjects)
• Intubated and requires mechanical ventilation (including ECMO) at time of randomization

• Exception: use of HFNC oxygen and noninvasive ventilation are permitted
• Endotracheal intubation is imminent, in the opinion of the investigator
• Not expected to survive for more than 48 hours after hospital admission, in the opinion of the investigator
• Presence of any of the following comorbid conditions before randomization and prior to SARS-CoV-2 infection:

• New York Heart Association class IV heart failure
• Stage 4 or 5 chronic kidney disease or requires renal replacement therapy
• Biopsy proven cirrhosis, portal hypertension or hepatic encephalopathy
• Stage IV malignancy
• Chronic lung disease requiring home oxygen
• Active tuberculosis
• History or evidence of pulmonary alveolar proteinosis
• Confirmed diagnosis or clinical suspicion of bacterial pneumonia or active uncontrolled bacterial, fungal, or non SARS-CoV-2 viral infection at Screening
• Absolute neutrophil count (ANC) value < 5 × 109 cells/L at Screening (can be lowered up to < 1.5 × 109 cells/L after Independent Data Monitoring Committee review of safety data, if CSL324 induced neutropenia is not assessed as a safety concern)
• Currently receiving a prohibited therapy including G-CSF, granulocyte-macrophage colony-stimulating factor (GM-CSF), or antibody against interleukin 6 (IL-6) / IL 6 receptor (anti IL-6 / 6R)

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

CSL Behring

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Other Identifiers

CSL324_COVID-19

Identifier Type: -

Identifier Source: org_study_id