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RecruitingNCT05640271Updated Sep 15, 2026

Tocilizumab for Acute Chest Syndrome

A Phase 2 interventional study of Tocilizumab in Sickle Cell Disease and Acute Chest Syndrome, sponsored by University of Chicago. Recruiting at 1 site in United States. Open to participants aged 12 Years and older. Per ClinicalTrials.gov, last updated 2026-09-15.

Sponsored by University of Chicago · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
200
Allocation
Randomized
Ages
12 Years and older
Sex
All
01

Study summary

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.

Read the detailed 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.

02

Conditions studied

  • Sickle Cell Disease
  • Acute Chest Syndrome
03

Who can participate

Ages eligible
12 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Adults ≥ 12 years of age
  • Prior diagnosis of sickle cell disease (Hb SS, Hb SC, Hb Sb+, and Hb Sb0)

Exclusion criteria

Exclusion Criteria:

  • Pregnant patients or breastfeeding mothers.
  • Prior treatment with gene therapy or a stem cell transplant.
  • Current enrollment in a clinical trial involving an FDA-regulated drug or biologic.
  • Current neutropenia (absolute neutrophil count \< 1000/mm\^3)
  • Current thrombocytopenia (platelet count \< 50,000 mm\^3)
  • Aspartate aminotransferase (AST) or alanine transaminase (ALT) \> 10 times the upper limit of normal (ULN)
  • History of tuberculosis (TB).
  • Positive purified protein derivative (PPD) TB screening test.
  • 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

04

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
200 participants (estimated)

Study arms

  • Experimental
    Early Tocilizumab

    This arm will receive tocilizumab 80 mg at the time of acute chest syndrome diagnosis and subsequent randomization. Then, two days later, they will receive 50 mL of normal saline.

    Drug: Tocilizumab

  • Active comparator
    Delayed Tocilizumab

    This arm will receive 50 mL of normal saline at the time of acute chest syndrome diagnosis and subsequent randomization. Then, two days later, they will receive tocilizumab 80 mg. Thus, this delayed arm will serve as a placebo comparator for the first 48 hours and then as an active comparator for the remaining duration on study.

    Drug: Tocilizumab

Interventions

  • DrugTocilizumab

    Tocilizumab 80 mg IV dose (one time per patient)

05

What researchers measure

Primary outcomes

  1. Time-weighted SaO2/FiO2 ratio

    Oxygenation data will be obtained as part of routine clinical care. All changes in pulse oximetry measurement that are documented in the chart will be recorded in an oxygen saturation case report form with the date and time from Day 0 to Day 4. These peripheral oxygen saturation (SpO2) measurements will serve as surrogates for SaO2. Additionally, all changes in the route of supplemental oxygen delivery, rate of supplemental oxygen delivery, and fraction of inspired oxygen (FiO2) will be recorded in a corresponding case report form with the date and time from Day 0 to Day 4. The time-weighted SaO2/FiO2 ratio, our primary endpoint, will be calculated based on these two case report forms.

    Time frame: Total of 4 days (Day 0 to Day 4)

Secondary outcomes

  1. Red cell exchange transfusion rate

    As part of routine clinical care by the inpatient team, patients may receive a red cell exchange transfusion. The study team will assess if participants received any exchange transfusions from Day 0 to Day 8, and if so, they will record the date of the first exchange transfusion and the total number of units transfused during that time period.

    Time frame: Total of 9 days (Day 0 to Day 8)

  2. Intensive Care Unit (ICU) transfer rate

    Patients will be assessed for if they were admitted directly to the intensive care unit (ICU) or if they were transferred from the general medicine floor to the ICU between Day 0 and Day 8. The date of transfer to the ICU will be recorded if applicable.

    Time frame: Total of 9 days (Day 0 to Day 8)

  3. Length of stay

    Patients will be assessed for their admission and discharge dates. Length of stay will be calculated based on those two dates.

    Time frame: Up to 3 months (Admission Date to Discharge Date)

  4. Readmission rate

    Patients will be assessed for readmission for 28 days from discharge. Readmission will be assessed at the University of Chicago as well as through any linked hospitals through Care Everywhere within the electronic medical record system. The date of readmission will be recorded if applicable.

    Time frame: Total of 29 days (Discharge Date to 28 days after discharge)

  5. Mortality rate

    Patients will be assessed for mortality from Day 0 to Day 28. The date of death will be recorded if applicable.

    Time frame: Total of 29 days (Day 0 to Day 28)

06

Study locations

1 of 1 sites recruiting
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT05640271
Lead sponsor
University of Chicago
Responsible party
Sponsor
First posted
Dec 7, 2022
Start date
Apr 10, 2023
Primary completion
Dec 2026 (estimated)
Completion
Jun 2027 (estimated)
Last update
Sep 15, 2026

Study contacts

Gabrielle Lapping-Carr, MD
Contact
glappingcarr@uchicago.edu
773-702-6808
Gabrielle Lapping-Carr, MD
principal investigator · University of Chicago

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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