The First Affiliated Hospital of Soochow University
Suzhou, Jiangsu, 215006, China
NCT Number: NCT06951971
This study is trying to evaluate the efficacy and safety of dose-modified Emapalumab and Ruxolitinib (E-Ru) regimens for the treatment of active hemophagocytic lymphohistiocytosis.
Trial opening soon.
Get Notified1 year–70 year
All sexes
Interventional
Phase 2 / Phase 3
Suzhou, Jiangsu, 215006, China
This clinical trial is designed to evaluate a new treatment strategy for patients with active Hemophagocytic Lymphohistiocytosis (HLH)-a rare but severe immune disorder characterized by excessive inflammation and immune system activation. HLH can be life-threatening if not treated effectively.
The study is prospective and multicenter, meaning it will be conducted at multiple hospitals and medical institutions, and patients will be followed over time to assess treatment outcomes.
We aim to test the combination of two medications:
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Emapalumab (1-2 mg/kg intravenously once weekly for 8 weeks) + Ruxolitinib (15-30 mg orally twice daily for 8 weeks)
Time frame: 60 days
overall survival (OS) rate at 60 days (2-month OS)
Time frame: 7, 14, 28, and 56 days
The ORR was defined as the percentage of patients with a complete response (CR), a partial response (PR), or an improvement in the measures of HLH.
Time frame: 7, 14, 28, and 56 days
Adverse events (AEs) were assessed according to the National Cancer Institute Common Terminology Criteria for Adverse Events, version 5.0 (CTCAE 5.0).
Time frame: 6 months
event-free survival, defined as the time from the first administration of E-Ru until no response on day 7, disease progression or death from any cause
Time frame: 6 months
OS (defined as the time from the first administration of E-Ru until death from any cause)
Time frame: 7, 14, 28, and 56 days
Changes in biomarkers between baseline and post-treatment.
Contact information is provided by the study sponsor or research team.
The First Affiliated Hospital of Soochow University
Other
A Multiple Center, Prospective, Single Arm, Phase III Clinical Study to Evaluate the Efficacy and Safety of Dose-modified Emapalumab and Ruxolitinib in the Treatment of Hemophagocytic Lymphohistiocytosis
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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