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Carisma Therapeutics to Present Engineered Cell Therapy Data at The American Association for Cancer Research Annual Meeting

First-in-Human Trial with CAR Macrophages Shows the Cell Therapy May Be Safe, Feasible for Solid Tumors

Phase 1 clinical trial shows the safety, feasibility of CAR-M cell therapy for solid tumors

Preliminary findings from Penn Medicine in an ongoing first-in-human clinical trial examining the safety, tolerability and feasibility of chimeric antigen receptor macrophage (CAR-M) has helped to establish the viability of this innovative immunotherapy, which advances the trailblazing scientific discovery of CAR T cell therapy- also pioneered at Penn- for solid cancer tumors and offers a promising new strategy in the fight against cancer.

Late-Breaking Abstracts Announced for the Society for Immunotherapy of Cancer s 36th Annual Meeting

Expanding PARP Inhibitor Benefits in Advanced Pancreatic Cancer

BRCA variants, results of a small phase II trial showed. A patient cohort with germline and somatic mutations, including PALB2, had a 6-month progression-free survival (PFS) of 59.5%, decreasing only slightly to 54.5% at 12 months with maintenance rucaparib (Rubraca). The overall response rate of 41.7% included patients with germline (g) and somatic (s) BRCA1/2 mutations and those with PALB2 variants. Two-thirds of patients obtained disease control with the PARP inhibitor, according to Kim A. Reiss, MD, of University of Pennsylvania Perelman School of Medicine in Philadelphia, and colleagues. The results supported and extended those from the practicing-changing POLO trial of olaparib (Lynparza) maintenance for g

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