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BioWorld - Thursday, April 16, 2026
Home » diffuse large B-cell lymphoma

Articles Tagged with ''diffuse large B-cell lymphoma''

Seven deaths and five adverse events cause ADC to halt enrollment in phase II cancer study

July 11, 2023
By Lee Landenberger
Seven deaths and five respiratory-related, treatment-emergent adverse events in a group of 40 aged and very unwell cancer patients rang alarm bells for ADC Therapeutics SA. The company has voluntarily paused enrollment in its phase II Lotis-9 study of Zynlonta (loncastuximab tesirine-lpyl) and rituximab (Lonca-R) for treating previously untreated diffuse large B-cell lymphoma in those who are considered frail or unfit.
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Curocell reports positive interim phase II results on Korean CAR T therapy, aims for NDA in 2024

June 20, 2023
By Marian (YoonJee) Chu
Curocell Inc. is inching closer to realizing Korea’s first domestically developed CAR T therapy, presenting “encouraging” interim phase II trial results for anbalcabtagene-autoleucel at the International Conference on Malignant Lymphoma in Lugano, Switzerland.
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Photomicrograph of diffuse large B-cell lymphoma

Genentech wins U.S. accelerated approval for lymphoma drug Columvi

June 16, 2023
By Karen Carey
Patients with an aggressive form of lymphoma who have failed prior therapies now have a new option for treatment with the U.S. FDA’s accelerated approval of Columvi (glofitamab-gxbm), which was granted under priority review a few weeks ahead of the July 1 PDUFA date.
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Cancer

Chia Tai Tianqing Pharmaceutical describes new BTK degradation inducers

June 13, 2023
Chia Tai Tianqing Pharmaceutical Group Co. Ltd. has identified proteolysis targeting chimeras (PROTACs) comprising cereblon (CRBN) ligands coupled to a Bruton tyrosine kinase (BTK) targeting moiety via linker and thus acting as BTK degradation inducers.
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Cancer

Ubix Therapeutics describes new BTK degradation inducers

May 30, 2023
Ubix Therapeutics Inc. has identified proteolysis targeting chimeras (PROTACs) comprising cereblon (CRBN) ligands coupled to a Bruton tyrosine kinase (BTK) targeting moiety via linker acting as BTK degradation inducers reported to be useful for the treatment of cancer and autoimmune disease.
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FDA approved icons and medical professional

Genmab, Abbvie to join Roche with FDA nod for CD20 bispecific in lymphoma

May 19, 2023
By Jennifer Boggs
Five months after the first anti-CD20xCD3 T-cell engaging bispecific antibody, Roche Holding AG’s Lunsumio (mosunetuzumab), cleared U.S. FDA approval for follicular lymphoma, partners Genmab A/S and Abbvie Inc. won the agency’s approval for epcoritamab as the first subcutaneous CD20xCD3 bispecific antibody for treating diffuse large B-cell lymphoma.
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Cancer

Jiangsu Chia Tai Tianqing presents new exportin-1 receptor antagonists

May 19, 2023
Jiangsu Chia Tai Tianqing Pharmaceutical Group Co. Ltd. has divulged exportin-1 (CRM1; XPO1) receptor antagonists reported to be useful for the treatment of lymphoma and leukemia.
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Photomicrograph of diffuse large B-cell lymphoma
Immuno-oncology

ABBV-319, novel CD19-targeting GRM ADC with efficacy in models of B-cell malignancies

April 28, 2023
Researchers from Abbvie Inc. recently presented the discovery and preclinical evaluation of a novel CD19-targeting glucocorticoid receptor modulator (GRM) agonist antibody-drug conjugate (ADC), ABBV-319, being developed for the treatment of B-cell malignancies.
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Photomicrograph of diffuse large B-cell lymphoma
Cancer

BTG1 mutations in germinal center B cells confer oncogenic transformation potential

Feb. 22, 2023
Diffuse large B-cell lymphomas (DLBCL) with mutations in B-cell translocation gene 1 (BTG1) present poor outcomes and extensive dissemination. Missense mutations of BTG1 are specific to germinal center-derived B cell lymphomas, which suggests an oncogenic function that depends on the specific cellular context. In a recent study published in Science, researchers from Weill Cornell Medicine and collaborators investigated how BTG1 mutations further contribute to the pathogenesis of these tumors.
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Dividing breast cancer cell.
Cancer

IHMT-337, a potent irreversible EZH2 inhibitor with efficacy in models of TNBC and DLBCL

Feb. 9, 2023
Previous research has demonstrated that overexpression or gain-of-function mutations of enhancer of zeste homolog 2 (EZH2) are significantly associated with tumor cell proliferation of a number of cancers.
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