Phase 1/2a Trial of BI-1206, a Monoclonal Antibody to CD32b (FcyRIIB), in Combination With Rituximab With or Without Acalabrutinib in Subjects With Indolent B-Cell Non-Hodgkin Lymphoma That Has Relapsed or is Refractory to Rituximab
Latest Information Update: 13 Jan 2026
At a glance
- Drugs Acalabrutinib (Primary) ; BI 1206 (Primary) ; BI 1206 (Primary) ; Rituximab
- Indications B-cell lymphoma; Follicular lymphoma; Mantle-cell lymphoma; Marginal zone B-cell lymphoma; Non-Hodgkin's lymphoma
- Focus Adverse reactions
- Sponsors BioInvent International
Most Recent Events
- 08 Dec 2025 According to a BioInvent International media release, among 15 evaluable patients in the safety run-in (data cut-off December 1, 2025), no differences in safety or efficacy were observed between the two dose levels, supporting continued enrollment into the trial's expansion phase.
- 08 Dec 2025 According to a BioInvent International media release, company announced the presentation of new data from the safety run-in portion of the trial evaluating BI-1206, in combination with rituximab and Calquence (acalabrutinib) for the treatment of non-Hodgkin's lymphoma (NHL) at the 2025 American Society of Hematology (ASH) Annual Meeting in Orlando, Florida.
- 08 Dec 2025 Results presented in a BioInvent International media release