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NCT Number: NCT06951971

Dose-modified Emapalumab and Ruxolitinib (E-Ru) Regimens for Hemophagocytic Lymphohistiocytosis

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.

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Key information

Age range

1 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

About this study

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:

  • Emapalumab, a monoclonal antibody that blocks interferon-gamma, a key driver of the overactive immune response seen in HLH. In this trial, it will be used at a lower-than-standard dose to reduce potential side effects.
  • Ruxolitinib, a JAK1/2 inhibitor that can reduce inflammation by interfering with immune signaling pathways. It will be administered at a higher-than-standard dose to enhance its therapeutic effects.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Fulfillment of at least five of the eight HLH-2004 criteria for HLH;
  • Age 1-70 years old;
  • No prior chemotherapy for HLH;
  • Confirmed not pregnant and willing to use effective contraceptive measures during the study period, with the last dose of medication administered at least 12 months prior;
  • Signed informed consent prior to study participation.

Exclusion criteria

  • According to the New York Heart Association (NYHA) score, patients with heart disease of grade II or above (including grade II);
  • HIV-infected patients;
  • Patients with severe renal dysfunction (glomerular filtration rate <15 mL/min);
  • Patients with severe liver cirrhosis (MELD score>20);
  • Uncontrollable infections (including lung infections, intestinal infections, etc.);
  • Have serious mental illness;
  • Have a history of active tumor;
  • Participate in other clinical investigators at the same time;
  • People with central nervous system involvement;
  • Exclusion criteria related to concomitant medication.

Treatment and study plan

dose-modified E-Ru

Drug

Emapalumab (1-2 mg/kg intravenously once weekly for 8 weeks) + Ruxolitinib (15-30 mg orally twice daily for 8 weeks)

Salvage treatment and follow-up

Other
  • for patients who did not respond to the E-Ru regimen after 7 days or who relapsed at any point during treatment, a rescue regimen such as HLH-94 or doxorubicin-etoposide-methylprednisolone (DEP) was administered; 2) for patients diagnosed with lymphoma after enrollment, chemotherapy was initiated; 3) for patients who completed 8 weeks of treatment without recurrence and had no detected HLH-related gene mutations, follow-up was initiated; and 4) for patients who met the criteria for allo-HSCT, allo-HSCT was performed.

Primary outcomes

  1. 60-days OS

    Time frame: 60 days

    overall survival (OS) rate at 60 days (2-month OS)

Secondary outcomes

  1. Response rate

    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.

  2. Security

    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).

  3. EFS

    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

  4. Overall survival

    Time frame: 6 months

    OS (defined as the time from the first administration of E-Ru until death from any cause)

  5. Trend of related indicators

    Time frame: 7, 14, 28, and 56 days

    Changes in biomarkers between baseline and post-treatment.

Study contacts

Contact information is provided by the study sponsor or research team.

Yue Song, Dr

CONTACT

[email protected]

+86 18810253070

Sponsors and collaborators

Lead sponsor

The First Affiliated Hospital of Soochow University

Other

Registry information

Official study title

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

Important dates

Study start
2025
Primary completion
2027
Study completion
2028
First posted
Apr 30, 2025
Registry last updated
Apr 30, 2025

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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