RecruitingEarly Phase 1NCT07376642
A Phase I/IIa, Open-label, Single-center, Dose-escalation and Dose-expansion Study to Evaluate the Safety, Tolerability, and Preliminary Efficacy of IMV101 as a Single Agent in Subjects With Relapsed/Refractory B-cell Non-Hodgkin Lymphoma
Studying B-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
- Suzhou Immunofoco Biotechnology Co., Ltd
- Intervention
- IMV101 treatment(drug)
- Enrollment
- 30 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2025 – 2027
Study locations (4)
- Cancer Hospital Chinese Academy of Medical Sciences, Beijing, Beijing Municipality, China
- Beijing GoBroad Boren Hospital, Beijing, Beijing Municipality, China
- Zhengzhou Yihe Hospital, Zhengzhou, Henan, China
- The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, 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.
Open NCT07376642 on ClinicalTrials.govOther trials for B-cell non-Hodgkin lymphoma
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