US FDA Grants Breakthrough Therapy Designation to Calderasib for KRAS G12C-Mutant NSCLC
Calderasib has received US FDA Breakthrough Therapy Designation for certain patients with newly diagnosed metastatic KRAS G12C-mutant Non-Small Cell Lung Cancer (NSCLC), supported by promising phase 1 KANDLELIT-001 trial data highlighting its potential as a next-generation, highly potent and selective KRAS G12C inhibitor.
Taiho Pharmaceutical | 30/05/2026 | By News Bureau | 108
US FDA Approves INQOVI Plus Venetoclax for AML
The US Food and Drug Administration (FDA) approves INQOVI with venetoclax as the first all-oral combination treatment for acute myeloid leukemia patients ineligible for intensive chemotherapy, supported by positive ASCERTAIN-V trial data.
Taiho Pharmaceutical | 14/05/2026 | By News Bureau | 121
JFCR, NEC and Taiho Partner on Whole-Genome Driven Cancer Vaccine Research
JFCR, NEC, and Taiho have launched a joint research initiative to develop novel cancer vaccines using whole-genome data. The project is part of AMED’s national programme on whole-genome analysis, supporting efforts to demonstrate its clinical utility and build systems that translate genomic insights into patient benefits.
Taiho Pharmaceutical | 01/12/2025 | By Dineshwori | 165
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