虽然BRAFV600E突变转移性结直肠癌患者面临极高的未满足医疗需求,但迄今为止,针对这部分初治患者的生物标志物驱动治疗产品尚未得到批准。此次辉瑞的组合疗法获得FDA加速批准,不仅为患者带来了全新的治疗选择,也为医药行业研究和开发高效疗法提供了新的方向与动力。
Pfizer’s BRAFTOVI combination regimen receives US FDA approval for treatment of metastatic colorectal cancer: New York Monday, December 23, 2024, 10:00 Hrs [IST] Pfizer Inc anno ...
We have summarized in this article the current state of combination therapy of approved targeted drugs and irradiation. Since the introduction of the first targeted compounds almost (trastuzumab ...
1 Office for Doctoral Studies, Charité-Universitätsmedizin Berlin, Berlin, Germany 2 Office for Postgraduate Student Studies, Kunming Medical University, Kunming, China lncRNAs (long non-coding RNAs) ...
Pfizer Inc. (NYSE: PFE) today announced that the U.S. Food and Drug Administration (FDA) has approved BRAFTOVI® (encorafenib) in combination with ...
NEW YORK, NY, USA I December 20, 2024 I Pfizer Inc. (NYSE: PFE) today announced that the U.S. Food and Drug Administration (FDA) has approved BRAFTOVI ® (encorafenib) in combination with cetuximab ...