Clazakizumab vs. Placebo - COVID-19 Infection

Recruiting now · Phase 2 · Has a placebo group

Conditions studied: COVID-19 Infection

In brief

The purpose of this study is to investigate the effectiveness and safety of treatment with clazakizumab compared to a placebo (inactive substance). We are proposing to try this drug to treat coronavirus disease 2019 (COVID-19) infection. Patients with COVID-19 infection have been shown to have increases in certain inflammatory processes. Clazakizumab is an antibody (immune system protein) that blocks certain inflammatory processes. The treatment plan is to attempt to inhibit or block these inflammatory processes in order to try to limit the damage COVID-19 causes to the lungs.

Key facts

Study ID

NCT04494724

Run by

The Methodist Hospital Research Institute

People needed

60

Starts

2020-07-13

Expected to finish

2021-07-31

Last updated by the study team

2020-07-31

Who can join

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

You may qualify if…

• Age >18 at the time of screening.
• Participant or legally authorized representative (LAR) must be able to understand and provide informed consent.
• Hospitalized with coronavirus disease (COVID-19) confirmed by polymerase chain reaction (PCR) assay from any specimen (eg, respiratory, blood, urine, stool, other bodily fluid) within the prior 72 hours.
• C-reactive protein (CRP) > 3.5 mg/dL
• Evidence of pulmonary involvement with at least 2 of the following:
• oxygen saturation at rest in ambient air with peripheral capillary oxygen saturation (SpO2) ≤ 94%
• tachypnea with resting respiration rate > 25 breaths/minute
• Partial pressure of oxygen (PaO2)/initial fraction of inspired oxygen (FiO2) ≤ 300 mmHg
• Chest imaging (radiograph, CT, or ultrasound) with abnormalities consistent COVID-19 pneumonia

You may not qualify if…

• Previous hypersensitivity or allergic reactions to clazakizumab
• Lactating or pregnant females
• Patients with latent tuberculosis (TB) and who are not receiving treatment
• Patients with active TB
• Patients with known active inflammatory bowel disease, untreated diverticulitis, or gastrointestinal perforation
• Requiring mechanical ventilation or extracorporeal membrane oxygenation (ECMO)
• A significantly abnormal general serum screening lab result defined as a white blood cell (WBC) count < 3.0 X 10\^3/mL, a hemoglobin (Hgb) < 8.0 g/dL, a platelet count < 50 X 10\^3/mL, an aspartate aminotransferase (AST) or alanine aminotransferase (ALT) > 5 times upper limit normal
• Participation in another clinical trial investigating COVID-19-aimed agents
• Presence of any medical or psychosocial condition, which the investigator believes, would hinder adherence to the study requirements.

Where it is running

• Houston Methodist Hospital — Houston, Texas, United States (enrolling)

Full record on ClinicalTrials.gov

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