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Clinical Trials Arena on MSNCullinan Therapeutics receives EMA approval for rheumatoid arthritis drug trialThe trial will assess the therapy’s pharmacokinetics, pharmacodynamics and safety, as well as its impact on disease activity.
This subcutaneous CD19/CD3-directed bispecific-TCE (BiTE) demonstrated deep B-cell depletion and a favourable safety profile with weekly injections in Phase 1 trials for non-Hodgkin’s lymphoma ...
The deal centres around TNB-486, a bispecific CD19 and CD3 T-cell engager in phase 1 testing in patients with relapsed and refractory B-cell non-Hodgkin lymphoma (NHL) who have received two or ...
Bargou et al. assessed the efficacy of blinatumomab—an antibody with dual specificity for CD19 and CD3 antigens—in patients with non-Hodgkin lymphoma who relapsed after standard treatments.
Cullinan Therapeutics rebranded from oncology to immunology+oncology, focusing on CD19 TCEs for autoimmune diseases. Check out my recommendation for CGEM.
Cambridge, Massachusetts Saturday, April 19, 2025, 15:00 Hrs [IST] ...
The panels used were (1) Immune Cell Composition (markers: CD45 VioBlue, CD4 VioGreen, CD3 FITC, CD56 PE, CD16 PE, 7AAD, CD19 PE-Vio770, CD14 APC, and CD8 APC-Vio770 from Miltenyi Biotec, Bergisch ...
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