Clinical trial results and effectiveness of talquetamab-tgvs
Talquetamab (talquetamab), as an innovative bispecific antibody drug, has proven its significant efficacy in patients with relapsed and refractory multiple myeloma (MM) in multiple clinical trials. Because multiple myeloma is a refractory disease, especially in patients who respond poorly to conventional treatments such as chemotherapy, proteasome inhibitors, and immunomodulators, taquitutumab demonstrates its importance as a new option for immunotherapy.
In a pivotal clinical phase III trial (such as MonumenTAL-1), tarquinatumumab showed significant overall response rate (ORR) and progression-free survival (PFS) when combined with standard treatment regimens (such as lenalidomide and dexamethasone), becoming a new highlight in the treatment of multiple myeloma. Data show that among patients treated with Taquitutumab, the overall response rate can reach 73%, and the complete response rate (CR) is also constantly improving. This result shows that Tacistumumab can significantly improve the patient's condition clinically, especially in drug-resistant myeloma cells. Tacistumumab can activate T cells and accurately kill tumor cells through the action of the immune system.
Progression-free survival (PFS) is an important indicator to measure anti-cancer efficacy, and the PFS of Taquitutumab also performed well. In clinical trials, the median PFS reached 9.2 months, far exceeding the results of the standard chemotherapy group. This data proves that when treating multiple myeloma, taquitumab can effectively delay the progression of the disease and provide patients with more survival time.
The overall survival time (OS) of Taquitumab is also an important indicator for evaluating the efficacy. In a clinical study, patients treated with taquitumab showed better survival than conventional treatment. This data supports the promise of tasitumumab in the treatment of multiple myeloma, especially in patients who have become resistant to traditional therapies.
Keyword tags: Talquetamab,Talquetamab, clinical trial, efficacy, overall response rate, progression-free survival, overall survival, cytokine release syndrome, multiple myeloma
Reference materials:https://www.talvey.com/
[ 免责声明 ] 本页面内容来自公开渠道(如FDA官网、Drugs官网、原研药厂官网等),仅供持有医疗专业资质的人员用于医学药学研究参考,不构成任何治疗建议或药品推荐。所涉药品可能未在中国大陆获批上市,不适用于中国境内销售和使用。如需治疗,请咨询正规医疗机构。本站不提供药品销售或代购服务。
.jpeg)