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Tocilizumab for Acute Chest Syndrome

Tocilizumab for Acute Chest Syndrome

Recruiting
18 years and older
All
Phase 2

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Overview

The investigators are evaluating the role of a low dose of tocilizumab in treating acute chest syndrome in patients with sickle cell disease. Tocilizumab inhibits interleukin-6 (IL-6) receptors and is used to treat rheumatoid arthritis and severe cytokine release syndrome, which can be seen with chimeric antigen receptor T-cell (CAR-T) therapy, and it is also authorized for treatment of COVID-19. Since IL-6 levels are elevated in the sputum of patients with acute chest syndrome, the investigators are hopeful that this will be an effective strategy. The investigators will be looking at how a low dose of tocilizumab affects oxygen status, clinical outcomes, and laboratory markers in patients admitted to the hospital with acute chest syndrome.

Description

In this randomized, placebo-controlled, double-blinded phase II study, enrolled patients admitted to the University of Chicago who are diagnosed with acute chest syndrome will receive one dose of tocilizumab 80 mg IV and one normal saline placebo dose. The order of these doses will be randomized at a 1:1 ratio. After collecting oxygenation data as a baseline for 8 hours, patients will then receive tocilizumab versus placebo as their early dose and then the opposite (placebo versus tocilizumab) 48 hours later. Clinical, laboratory, and patient-reported outcome data will be collected during their admission and compared between arms.

Eligibility

Inclusion Criteria:

  • Adults ≥ 18 years of age
  • Prior diagnosis of sickle cell disease (Hb SS, Hb SC, Hb Sb+, and Hb Sb0)

Exclusion Criteria:

  • Pregnant patients or breastfeeding mothers.
  • On active therapy with a Bruton's tyrosine kinase-targeted agent, which include the
    following

Acalabrutinib Ibrutinib Zanubrutinib

  • On active therapy with a JAK2-targeted agent, which include the following:

Baricitinib Ruxolitinib Tofacitinib Upadacitinib

  • Any of the following biologic immunosuppressive agent (and any biosimilar versions thereof) administered in the past 6 months:
        Abatacept Adalimumab Alemtuzumab Atezolizumab Belimumab Blinatumomab Brentuximab
        Certolizumab Daratumumab Durvalumab Eculizumab Elotuzumab Etanercept Gemtuzumab Golimumab
        Ibritumomab Infliximab Inotuzumab Ipilimumab Ixekizumab Moxetumomab Nivolumab Obinutuzumab
        Ocrelizumab Ofatumumab Pembrolizumab Polatuzumab Rituximab Sarilumab Secukinumab
        Tocilizumab Tositumumab Tremelimumab Urelumab Ustekinumab

Study details
    Sickle Cell Disease
    Acute Chest Syndrome

NCT05640271

University of Chicago

27 January 2024

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