A Study to Evaluate the Efficacy, Safety and Pharmacokinetics of Emapalumab in Adult Patients With HLH

PHASE2/PHASE3TerminatedINTERVENTIONAL
Enrollment

7

Participants

Timeline

Start Date

June 2, 2020

Primary Completion Date

June 29, 2021

Study Completion Date

June 29, 2021

Conditions
Hemophagocytic Lymphohistiocytoses
Interventions
DRUG

Emapalumab-Lzsg

Patients were administered Emapalumab-Lzsg by intravenous (i.v.) infusion over a period of 1 to 2 hours, at an initial dose of 6 mg/kg and continued at 3 mg/kg, every 3 days for the first 2 weeks (Study Day \[SD\] 15), and then twice-a-week. If the treating physician deemed appropriate, the dose of emapalumab could be increased (up to 10 mg/kg), guided by clinical and laboratory response.

Trial Locations (1)

77030

MD Anderson Cancer Center, Houston

All Listed Sponsors
collaborator

Light Chain Bioscience - Novimmune SA

INDUSTRY

lead

Swedish Orphan Biovitrum

INDUSTRY