CompletedPhase 4NCT05744063
A Post-authorization Study to Describe the Safety and Efficacy of Emapalumab for the Treatment of pHLH in Treatment Experienced Chinese Patients
Studying Acquired hemophagocytic lymphohistiocytosis associated with malignant disease
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Swedish Orphan Biovitrum
- Principal Investigator
- Rui Zhang, MD, ProfBeijing Children's Hospital
- Intervention
- Emapalumab-Lzsg 5 MG/ML [Gamifant](drug)
- Enrollment
- 13 enrolled
- Eligibility
- All sexes
- Timeline
- 2023 – 2025
Study locations (7)
- Swedish Orphan Biovitrum Research site, Shanghai, Fudan, China
- Swedish Orphan Biovitrum Research site, Beijing, Xicheng, China
- Swedish Orphan Biovitrum Research site, Beijing, China
- Swedish Orphan Biovitrum Research site, Chongqing, China
- Swedish Orphan Biovitrum Research site, Guangzhou, China
- Swedish Orphan Biovitrum Research site, Nanjing, China
- Swedish Orphan Biovitrum Research site, Zhengzhou, China
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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