Trials / Unknown
UnknownNCT02631109
L-DEP Regimen as a Salvage Therapy for Refractory Epstein Barr Virus-induced Hemophagocytic Lymphohistiocytosis
- Status
- Unknown
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 120 (estimated)
- Sponsor
- Beijing Friendship Hospital · Academic / Other
- Sex
- All
- Age
- 14 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
This study aimed to investigate the efficacy and safety of Pegaspargase together with liposomal doxorubicin, etoposide and high dose methylprednisolone (L-DEP) as a salvage therapy for refractory Epstein Barr virus-induced hemophagocytic lymphohistiocytosis.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Pegaspargase | 2000U/m2 day5 |
| DRUG | doxorubicin | 25mg/m2 day1 |
| DRUG | etoposide | 100 mg/m2 was administered once on the first day of every week |
| DRUG | methylprednisolone | 15 mg/kg days 1 to 3, 0.75 mg/kg days 4 to 7 |
Timeline
- Start date
- 2015-12-01
- Primary completion
- 2017-11-01
- Completion
- 2019-11-01
- First posted
- 2015-12-16
- Last updated
- 2016-08-04
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT02631109. Inclusion in this directory is not an endorsement.