Emapalumab Treatment For Anticipated Clinical Benefit In Sepsis Driven By The Interferon-Gamma Endotype (The EMBRACE Trial)

Hellenic Institute for the Study of Sepsis

Status and phase: Enrolling; Phase 2

Conditions: Sepsis

Treatments: Drug: Emapalumab-Izsg; Drug: Placebo

Study type: Interventional

Funder types: Other

Identifiers

NCT06694701

EMBRACE

2024-515255-38-00 (EU Trial (CTIS) Number)

Details and patient eligibility

About

EMBRACE is a double-blind, randomized, placebo-controlled, phase IIa study that will be conducted in multiple Intensive Care Units (ICUs) and departments of Internal Medicine across Greece. It aims to investigate if treatment with emapalumab, a monoclonal antibody which blocks IFNγ, may improve the outcome of patients with sepsis driven by the IDS (endotype of IFNγ-driven sepsis) endotype. EMBRACE also aims to identify the best dosing regimen of emapalumab for the management of IDS.

Full description

The EMBRACE trial aims to generate proof-of-concept if treatment with emapalumab, a monoclonal antibody which blocks IFNγ signaling, may improve the outcome of patients with sepsis driven by the IDS endotype. In EMBRACE, two different dose regimens of emapalumab are administered in order to: a) investigate which dose regimen may provide most of efficacy in the decrease of SOFA score, a new endpoint for sepsis suggested already by others; b) investigate which dose regimen better attains the pharmacodynamic goal of emapalumab defined as the decrease of blood CXCL9; and c) compare the efficacy of the two dose regimens with placebo treated patients.

Enrollment: 75 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Provide written informed consent
• Adults (≥18 years) of male or female sex
• Diagnosis of community-acquired pneumonia (CAP), hospital-acquired pneumonia (HAP), ventilator-associated pneumonia (VAP), intrabdominal infection (IAI), acute pyelonephritis (AP), primary bloodstream infection (BSI) and viral respiratory infections.
• Sepsis defined by the Sepsis-3 definitions. This is defined as any new infection which is accompanied by an increase of the total baseline SOFA score by at least 2 points. The total baseline SOFA score is calculated by the medical comorbidities and by the evaluation of clinical variables before the sepsis episode in the case of hospital-acquired sepsis. In the case of patients with unknown baseline SOFA score, sepsis is defined as any new infection accompanied by total SOFA score 2 or more.
• Willingness to use effective contraceptive methods during the period from the start of the study drug to 6 months after the administration of the last dose of the study drug, in patients of reproductive age.
• Serological documentation of IDS defined as detectable blood IFNγ and CXCL9 more than 2,200 pg/ml. IFNγ and CXCL9 are measured in the central study lab by an enzyme immunosorbent assay.
• Absence of sepsis-induced immunoparalysis (SII). This is defined as ≥8000 of HLA-DR receptors on CD45/CD14-monocytes measured by flow-cytometry in the central lab using the BD™ fluorescence assay9.

Exclusion criteria

• Body weight more than 104 kg
• Intake of any other biological during the last 30 days prior screening except for the intake of anakinra or tocilizumab for patients with active infection by SARS-CoV-2
• Intake of any Janus kinase inhibitors during the last 30 days prior screening except for the intake of baricitinib for patients with active infection by SARS-CoV-2
• Known active infection by Mycobacterium tuberculosis or other mycobacteria. These patients may be enrolled in the trial if treatment against infection by Mycobacterium tuberculosis or other mycobacteria has been initiated
• Known active infection by VZV (varicella zoster virus) or by Histoplasma capsulatum or by Leishmania spp. These patients may be enrolled in the trial if treatment against infection by VZV or Histoplasma capsulatum has been initiated
• Known active infection by the hepatitis B virus, by the hepatitis C virus and by cytomegalovirus
• Vaccination the last 12 weeks before screening with BCG vaccine
• Vaccination with any live or attenuated live vaccine (other than BCG) the last 12 weeks before screening
• Known allergy or hypersensitivity reactions to emapalumab
• Patients living with the human immunodeficiency virus (HIV)
• Patients with stage IV solid or hematologic malignancy
• Patients with neutropenia (less than 1,000 neutrophils/mm3)
• Patients transplanted for solid organ or stem cells
• Pregnancy or lactation
• Participation in any other interventional trial the last 28 days prior to day 1

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

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75 participants in 3 patient groups, including a placebo group

Placebo

Placebo Comparator group

Description:

Standard-of-care (SoC) treatment and placebo drug.

Treatment:

Drug: Placebo

Emapalumab Group 1

Active Comparator group

Description:

SoC treatment and a low dose of emapalumab.

Treatment:

Drug: Emapalumab-Izsg

Drug: Emapalumab-Izsg

Emapalumab Group 2

Active Comparator group

Description:

SoC treatment and a high dose of emapalumab.

Treatment:

Drug: Emapalumab-Izsg

Drug: Emapalumab-Izsg