Glofitamab in Chinese Patients With R/R DLBCL
Recruiting now
Conditions studied: DLBCL - Diffuse Large B Cell Lymphoma
In brief
This study will evaluate the safety and efficacy of glofitamab as a single agent in Chinese patients with relapsed or refractory (R/R) diffuse large B-cell lymphoma (DLBCL) who have failed two or more lines of systemic therapy.
Key facts
- Study ID
- NCT06481826
- Run by
- Peking Union Medical College Hospital
- People needed
- 20
- Starts
- 2024-01-01
- Expected to finish
- 2028-12-31
- Last updated by the study team
- 2026-03-27
Who can join
Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Histologically-confirmed DLBCL
- Participants must have relapsed or failed to respond to at least two lines of prior systemic therapy
- Participants must have measurable disease
You may not qualify if…
- Pregnancy or breastfeeding
- Patient with known active infection, or reactivation of a latent infection
- Patient with active autoimmune disease or immune deficiency
- severe organ failure:LVEF<40%;DLCO<40%;eGFR<30ml/min;Bilirubin≥3ULN
- Patients who are dependent on the sponsor, the investigator or the trial site
Where it is running
- Peking Union Medical College Hospital — Beijing, Beijing Municipality, China (enrolling)
Full record on ClinicalTrials.gov
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