Active, not recruitingPHASE1, PHASE2NCT04077723
A Study to Evaluate the Safety, Pharmacokinetics and Preliminary Anti-Tumor Activity of Englumafusp Alfa in Combination With Obinutuzumab and in Combination With Glofitamab Following a Pre-Treatment Dose of Obinutuzumab in Participants With Relapsed/Refractory B-Cell Non-Hodgkin's 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
- Hoffmann-La Roche
- Principal Investigator
- Clinical TrialsHoffmann-La Roche
- Intervention
- Englumafusp alfa(drug)
- Enrollment
- 498 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2019 – 2027
Study locations (30)
- City of Hope Medical Center, Pasadena, California, United States
- University of California San Francisco, San Francisco, California, United States
- Colorado Blood Cancer Institute (CBCI) at Presbyterian/ St. Luke's Medical Center, Denver, Colorado, United States
- Beth Israel Medical Center, Boston, Massachusetts, United States
- Washington University School of Medicine, St Louis, Missouri, United States
- MSKCC, New York, New York, United States
- OhioHealth Research Institute, Columbus, Ohio, United States
- SCRI Oncology Partners, Nashville, Tennessee, United States
- South Austin Medical Center, Austin, Texas, United States
- The University of Texas MD Anderson Cancer Center, Houston, Texas, United States
- Peter Maccallum Cancer Centre, Melbourne, Victoria, Australia
- The Alfred Hospital, Melbourne, Victoria, Australia
- UZ Gent, Ghent, Belgium
- Queen Elizabeth II Health Sciences Centre, Halifax, Nova Scotia, Canada
- Jewish General Hospital, Montreal, Quebec, Canada
- +15 more locations on ClinicalTrials.gov
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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