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Phase 3 N=35 Treatment

Study to Assess the Efficacy and Safety of Emapalumab in Primary Haemophagocytic Lymphohistiocytosis

Primary Hemophagocytic Lymphohistiocytosis

Enrolled (actual)
35
Serious AEs
91.4%
Results posted
Mar 2024
Primary outcome: Primary: Overall Response at Week 8 or End of Treatment (if Earlier) — 62.9; 50.0; 73.7 Percentage of participants — p=0.0053

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
Emapalumab (Drug)
Age
Pediatric, Adult
Sex
All
Sponsor
Swedish Orphan Biovitrum
Primary completion
Aug 2021

Outcome Measures

OutcomeResultp-value
PRIMARY
Overall Response at Week 8 or End of Treatment (if Earlier)
62.9; 50.0; 73.7 0.0053 sig
SECONDARY
Overall Survival at End of Study
19; 9; 10; 1; 0; 1
SECONDARY
Overall Survival to HSCT
25; 12; 13
SECONDARY
Overall Survival for Patients Receiving HSCT
17; 8; 9
SECONDARY
Event-free Survival
16; 8; 8
SECONDARY
Overall Response at Start of Conditioning
4; 3; 1; 11; 5; 6
SECONDARY
Duration of Response
61; 40; 61
SECONDARY
Time to Response
4; 5; 4
SECONDARY
Number of Patients Reducing Glucocorticoids by 50% or More of the Baseline Dose During Emapalumab Treatment
15; 8; 7
SECONDARY
Number of Patients Proceeding to HSCT
23; 11; 12
SECONDARY
Quality of Life Assessed Through PedsQL™, Pediatric Quality of Life Inventory™
0.208; -6.514; 5.810; 0.794; 0.794; 8.469
SECONDARY
Quality of Life Assessed Through Behavioral, Affective and Somatic Experiences Scales (BASES)
10.0; 9.4; 10.5; 9.3; 9.6; 9.1
SECONDARY
Incidence, Severity, Causality and Outcomes of AEs (Serious and Non-serious)
15; 5; 10; 35; 16; 19
SECONDARY
Evolution of Laboratory Parameters Change From Baseline to EOT/Week 8
6; 3; 3; 2; 0; 2
SECONDARY
Number of Patients Who Discontinued Emapalumab Treatment
7; 3; 4

Summary

The purpose of this study is to expand the knowledge on the efficacy and safety of emapalumab (previously known as NI-0501) as a treatment for primary haemophagocytic lymphohistiocytosis (HLH) patients, including on long-term outcomes and quality of life assessments. Emapalumab can be administered as the first-line therapy to patients not previously treated with the current standard of care, or can be given to patients who have either failed or were unable to tolerate the available standard of care. Emapalumab is to be administered until the start of conditioning for hematopoietic stem cell transplantation (HSCT), with an anticipated duration ranging from a minimum of 4 weeks to approximately 12 weeks and not exceeding 6 months. After treatment completion, patients will continue in the study for long-term follow-up until 1 year after either HSCT or last emapalumab infusion (if HSCT is not performed).

Eligibility Criteria

Main Inclusion Criteria:

  • Primary HLH patients with active disease.
  • Treatment naïve patients or patients having already received HLH conventional therapy, but having not responded, not achieved a satisfactory response or worsened, or reactivated, or are unable to tolerate current standard of care.
  • Informed consent signed by the patient or by the patient's legally authorized representative.
  • Received guidance on contraception.

Main Exclusion Criteria:

  • Diagnosis of secondary HLH consequent to a proven rheumatic, metabolic or neoplastic disease.
  • Active mycobacteria, Histoplasma capsulatum, Shigella, Salmonella, Campylobacter or Leishmania infections.
  • Evidence of latent tuberculosis.
  • Presence of malignancy.
  • Concomitant disease or malformation severely affecting cardiovascular, pulmonary, central nervous system (CNS), liver, or renal function, that in the opinion of the Investigator may significantly affect the likelihood to respond to treatment and/or the assessment of emapalumab safety and/or efficacy.
  • History of hypersensitivity or allergy to any component of the study regimen.
  • Receipt of a BCG vaccine within 12 weeks prior to Screening.
  • Receipt of a live or attenuated-live (other than BCG) vaccine within 6 weeks prior to Screening.
  • Pregnant or lactating female patients.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03312751). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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