RecruitingPHASE1, PHASE2NCT04440436
Assessment of Safety and Efficacy of IM19 for Recurrent or Refractory (R/R) Non-Hodgkin's Lymphoma(NHL) Patients
Studying T-cell non-Hodgkin lymphoma
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
- Beijing Immunochina Medical Science & Technology Co., Ltd.
- Principal Investigator
- Yuqin Song, MD, PhDPeking University Cancer Hospital & Institute
- Intervention
- IM19 CAR-T Cells(drug)
- Enrollment
- 52 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2020 – 2035
Study locations (1)
- Beijing Cancer Hospital, Beijing, Beijing Municipality, China
Collaborators
Jiangsu Simcere Pharmaceutical Co., Ltd.
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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