Active, not recruitingPHASE1, PHASE2NCT05428969
A Study to Assess Safety, Tolerability and Preliminary Efficacy of Bexmarilimab in Combination With Standard of Care in Patients With Hematological Malignancies
Studying Acute myelomonocytic leukemia
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
- Faron Pharmaceuticals Ltd
- Principal Investigator
- Mika Kontro, MD, PhDHelsinki University Central Hospital
- Intervention
- Bexmarilimab(drug)
- Enrollment
- 181 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2022 – 2027
Study locations (10)
- City of Hope National Medical Center, Duarte, California, United States
- Yale Cancer Center, New Haven, Connecticut, United States
- UNC Lineberger Comprehensive Cancer Center, Chapel Hill, North Carolina, United States
- University of Texas, MD Anderson Cancer Center, Houston, Texas, United States
- Helsinki University Hospital, Helsinki, Finland
- Kuopio University Hospital, Kuopio, Finland
- Oulu University Hospital, Oulu, Finland
- Tampere University Hospital, Tampere, Finland
- The Christie NHS Foundation Trust, Manchester, United Kingdom
- Royal Cornwall Hospitals NHS Trust, Truro, United Kingdom
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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