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FDA grants accelerated approval to Brukinsa for advanced follicular lymphoma

FDA grants accelerated approval to Brukinsa for advanced follicular lymphoma
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Zanubrutinib-brukinsa , Mindy-valcarcel , Bymatthew-shinkle , Genentech ,

Advancing Treatment Selection in CLL Management

Treatment options are distinct in their mechanisms, safety profiles, and implications for patients’ quality of life.

United-states , United-kingdom , Chicago , Illinois , Milano , Lombardia , Italy , Italian , American , Eli-lilly , Zanubrutinib-brukinsa , Pirtobrutinib-jaypirca

Zanubrutinib Showcases Sustained PFS Benefit Vs Ibrutinib in R/R CLL/SLL

Zanubrutinib continued to demonstrate improved progression-free survival benefit over ibrutinib in the treatment of patients with relapsed/refractory chronic lymphocytic leukemia and small lymphocytic lymphoma, according to extended follow-up data from the phase 3 ALPINE trial.

Boston , Massachusetts , United-states , Dana-farber-cancer-institute , Zanubrutinib-brukinsa , Jenniferr-brown , Hematologic-malignancies , Margaret-collette-professor , Hematologic-oncology , Harvard-medical-school , Zanubrutinib

Treatment Opportunities Continue to Advance in CLL Management

In crafting a patient-centered regimen, the convergence of expertise from physicians and pharmacists, paired with the values and preferences of patients, becomes paramount.

United-states , United-kingdom , Milano , Lombardia , Italy , American , Italian , Amir-ali , Zanubrutinib-brukinsa , Eli-lilly , Yijun-caiis , Pirtobrutinib-jaypirca

Zanubrutinib Sustains Response, Safety Benefits Vs Ibrutinib in Waldenström Macroglobulinemia

Zanubrutinib Sustains Response, Safety Benefits Vs Ibrutinib in Waldenström Macroglobulinemia
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ASCO 2023: Leukemia and Lymphoma

Results include a landmark study that involved seamless collaboration across adult and pediatric patient groups, leading to a highly diverse study population. Other coverage addresses access to novel therapies and what's coming in the pipeline, including CAR T-cell therapy with tyrosine kinase inhibitors.

Texas , United-states , Houston , Philadelphia , Pennsylvania , California , Baylor-college-of-medicine , American , Rawan-faramand , Al-hadidi , Alex-francisco-herrera , Jason-westin

FDA Accepts sNDA for Zanubrutinib Plus Obinutuzumab for R/R Follicular Lymphoma

Following positive phase 2 results from the ROSEWOOD study, BeiGene is seeking FDA approval of zanubrutinib plus obinutuzumab for select patients with relapsed/refractory (R/R) follicular lymphoma.

Mehrdad-mobasher , Zanubrutinib-brukinsa , Prescription-drug-user-fee , Gene-announces , Follicular-lymphoma , Lymphoma ,

Zanubrutinib Plus Obinutuzumab and Venetoclax Induces High Undetectable MRD Rate in CLL/SLL

Zanubrutinib plus obinutuzumab and venetoclax demonstrated lasting responses characterized by sustained progression-free survival and undetectable minimal residual disease in peripheral blood and bone marrow in previously untreated patients with chronic lymphocytic leukemia or small lymphocytic lymphoma.

Massachusetts , United-states , Boston , Zanubrutinib-brukinsa , Jacob-soumerai , International-workshop , International-conference-on-malignant-lymphoma , Hospital-cancer-center , Annual-international-conference , Massachusetts-general-hospital-cancer-center ,

An Overview of the Specialty Therapy Pipeline in 2023

At the first business session of Asembia 2023, Ray Tancredi, divisional vice president at Walgreens, provided updates to the 2023 specialty therapy pipeline.

United-states , Americans , Mavacamten-camzyos , Ray-tancredi , Deucravacitinib-sotyktu , Zanubrutinib-brukinsa , Walgreens , Orphan-drug-act , Asembia , Specialty-therapy-pipeline , Oncology , Rare-disease