
Bhagirathbhai Dholaria
Articles
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2 months ago |
cgtlive.com | Bhagirathbhai Dholaria |Noah Stansfield
Poseida Therapeutics is currently evaluating P-BCMA-ALLO1, an allogeneic BCMA-directed chimeric antigen receptor T-cell (CAR-T) therapy, in an ongoing phase 1/1b clinical trial (NCT04960579) for the treatment of relapsed/refractory (r/r) multiple myeloma (MM).
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2 months ago |
cancernetwork.com | Luciano Costa |Bhagirathbhai Dholaria |Carl Ola Landgren |Muhamed Baljevic
February 11, 2025By Panelists discuss key strides made in 2024, including exciting data presented at the 66th American Society of Hematology Annual Meeting and Exposition (ASH 2024), and reflect on pivotal developments, such as new insights into Bruton tyrosine kinase inhibitors, that are shaping clinical practice while looking ahead to 2025 with anticipation for continued advancements that will further enhance treatment strategies and patient outcomes.
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2 months ago |
cancernetwork.com | Luciano Costa |Bhagirathbhai Dholaria |Carl Ola Landgren |Muhamed Baljevic
February 11, 2025By Panelists discuss how bispecifics, like teclistamab, are administered at their institutions, the monitoring of cytokine release syndrome (CRS) and immune effector cell–associated neurotoxicity syndrome (ICANS) during step-up dosing, and strategies to improve care transitions between academic centers and community practices.
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2 months ago |
cancernetwork.com | Luciano Costa |Bhagirathbhai Dholaria |Carl Ola Landgren |Muhamed Baljevic
February 11, 2025By Panelists discuss how bispecifics are sequenced with other B-cell maturation antigen (BCMA)–targeted therapies, such as chimeric antigen receptor (CAR) T cells or antibody drug conjugates (ADCs), and whether early vs late relapse impacts treatment strategies for relapsed/refractory multiple myeloma (R/R MM), with emphasis on how biological and clinical factors influence decision-making.
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2 months ago |
nature.com | Luciano Costa |Binod Dhakal |Bhagirathbhai Dholaria |Saurabh Chhabra
Response and progression criteria are necessary for any malignancy to standardize assessment of efficacy across trials. In multiple myeloma (MM), the International Myeloma Working Group (IMWG) established universally accepted criteria for response and progressive disease (PD) anchored on serum and urine paraprotein as primary biomarkers of disease burden [1]. The therapeutic landscape of newly diagnosed MM (NDMM) evolves rapidly.
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