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A clinical study of ruxolitinib combined with reduced-dose HLH-1994 regimen in the treatment of adult hemophagocytic lymphohistiocytosis

A clinical study of ruxolitinib combined with reduced-dose HLH-1994 regimen in the treatment of adult hemophagocytic lymphohistiocytosis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500115370
Enrollment
Unknown
Registered
2025-12-25
Start date
2025-12-29
Completion date
Unknown
Last updated
2026-01-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

hemophagocytic lymphohistiocytosis

Interventions

Intervention group:Ruxolitinib combined with the reduced-dose LH-1994 regimen for the induction therapy of adult hemophagocytic lymphohistiocytosis

Sponsors

Shandong Provincial Qianfoshan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1.Age >=18 years; 2.The patient has not received HLH treatment and was in an active state of HLH at the time of enrollment; 3.Patients who received glucocorticoid treatment before enrollment but still had active HLH after assessment could be included in this study (the dosage of glucocorticoids in the previous period should be noted at the time of enrollment). 4.For HLH secondary to rheumatic immune diseases, those who have no response after one week of glucocorticoid treatment; 5.The patient signed the informed consent form;

Exclusion criteria

Exclusion criteria: 1.Patients with definite active infections, such as leishmania, brucellosis, histoplasmosis, fungal infections or other uncontrollable bacterial infections, or HIV-infected individuals; 2.Patients with severe central nervous system involvement; 3.Patients with active massive hemorrhage of internal organs (including massive hemorrhage of the digestive tract, intracranial hemorrhage, alveolar hemorrhage, etc.); 4.Patients participating in other clinical studies at the same time; 5.Patients cannot be followed up;

Design outcomes

Primary

MeasureTime frame
Complete response rate;Overall response rate, ORR;

Secondary

MeasureTime frame
Adverse events;1-year overall survival rate;

Countries

China

Contacts

Public ContactGuangqiang Meng

Shandong Provincial Qianfoshan Hospital

menggq2001@163.com+86 531 89269106

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026