NASHPharmacologic Inhibition of FASN Reverses Diet-Induced Steatohepatitis in Mice and Inhibits Lipogenesis in Humans. By Graviton / 10/2017 AASLD
OncologyFirst in human study of the first-in-class fatty acid synthase (FASN) inhibitor TVB-2640 By Graviton / 04/2017 AACR Annual Meeting
NASHEstablishing the foundation for a novel, first-in-class, fatty acid synthase inhibitor, TVB-2640, for the treatment of NASH By Graviton / 04/2017 EASL International Liver Congress
OncologyFatty Acid Synthase – Modern Tumor Cell Biology Insights into a Classical Oncology Target By natalia / 02/2017 Pharmacology and Therapeutics
OncologyHeavily Pre-Treated Breast Cancer Patients show Promising Responses in the First in Human Study of the First-In-Class Fatty Acid Synthase (FASN) Inhibitor, TVB-2640 in Combination with Paclitaxel By Graviton / 12/2016 San Antonio Breast Cancer Symposium
OncologyFASN inhibition and taxane treatment combine to enhance anti-tumor efficacy in diverse xenograft tumor models through disruption of tubulin palmitoylation and microtubule organization and FASN inhibition-mediated effects on oncogenic signaling and gene expression By natalia / 12/2016 EBioMedicine
NASHPharmacological inhibition of FASN Prevents High Fat Diet Induced Liver Damage in Mice and Significantly Reduces de novo Lipogenesis in Humans By Graviton / 11/2016 AASLD The Liver Meeting
OncologyPreliminary Activity in the First in Human Study of the First-In-Class Fatty Acid Synthase Inhibitor, TVB-2640 By Graviton / 11/2016 NCRI Cancer Conference
OncologyMechanism and rationale for inhibition of FASN as a novel therapy for KRAS-mutant non-small cell lung cancer patients By natalia / 09/2016 Precison: Lung Cancer R&D Summit
OncologyDeNovo Palmitate Synthesis Supports Oncogenic Signaling Through Diverse Mechanisms: Implications for FASN-Targeted Therapeutics By natalia / 08/2016 Journal of Cell Signaling