Incb053914
WebNov 26, 2024 · INCB053914 is a recently described pan-PIM kinase inhibitor that exhibits potent activity against PIM1, PIM2, and PIM3 (biochemical 50% inhibitory concentration [IC 50] values of 0.24, 30, and 0.12 nM, respectively). 40 To assess the effects of INCB053914 on JAK2 V617F -driven cell growth, we determined the concentration for 50% of maximal … WebINCB053914 inhibits tumor growth in a dose-dependent manner in mice bearing MOLM-16 (AML) or KMS-12-BM (MM) tumors. A pharmacokinetic analysis of INCB053914 plasma …
Incb053914
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WebAug 1, 2015 · The in vitro and in vivo activity of INCB053914, a pan-PIM kinase inhibitor, was determined in a panel of acute myelogenous leukemia (AML) cell lines. Greater than half of all AML cell lines... WebNov 26, 2024 · INCB053914 is a recently described pan-PIM kinase inhibitor that exhibits potent activity against PIM1, PIM2, and PIM3 (biochemical 50% inhibitory concentration …
WebJan 14, 2024 · Chemsrc provides INCB053914 phosphate(CAS#:2088852-47-3) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of INCB053914 phosphate are included as well. WebINCB053914 (INCB-053914) is a novel potent, and selective ATP-competitive, pan-PIM kinase inhibitor with IC50 of 0.24/30.0/0.12 nM for PIM1/2/3, respectively. Purity : >98% …
WebStudy of INCB053914 in Subjects With Advanced Malignancies Jacksonville, FL This is an open-label, dose-escalation study of the proviral integration site of Moloney murine leukemia virus (PIM) kinase inhibitor INCB053914 in subjects with advanced malignancies. The study will be conducted in 4 parts. WebINCB053914 (INCB-053914) is a novel potent, and selective ATP-competitive, pan-PIM kinase inhibitor with IC50 of 0.24/30.0/0.12 nM for PIM1/2/3, respectively; INCB053914 is …
WebDec 7, 2024 · INCB053914 is currently under investigation in a Phase 1/2 study in patients with advanced hematological malignancies (ClinicalTrials.gov: NCT02587598). Our findings support a clinical study investigating the combination of INCB053914 and ruxolitinib in MPN patients. Disclosures Collins: Incyte Corporation: Employment, Equity Ownership.
WebApr 21, 2024 · Phase 1. Detailed Description: This is a prospective, single-center phase I clinical study aimed at determining the maximum-tolerated dose and safety of … bing search ignore siteWebDec 7, 2024 · Conclusions: INCB053914 monotherapy demonstrated preliminary safety in Part 1; elevated ALT/AST were the most common treatment-related TEAEs and DLTs, and … bing search i delete clear all historyWebSep 26, 2024 · A Safety and Tolerability Study of INCB053914 in Combination With INCB050465 in Diffuse Large B-Cell Lymphoma A Phase 1b, Multicenter, Open-Label Study of the Safety and Tolerability of INCB053914 in Combination With INCB050465 in Participants With Relapsed or Refractory Diffuse Large B-Cell Lymphoma Overall Status Completed … bing search images stretchedWebJun 21, 2024 · INCB053914 potently inhibited the activities of all three PIM isozymes, which is important for avoiding compensatory activity and for maximizing therapeutic efficacy [33, 34, 73]. PIM447 and AZD1208 are also potent and selective pan-PIM inhibitors that show similar activity in vitro and in vivo to INCB053914 [35, 37, 54]. bing search icon downloadWeb#5b3914 Color Information. Information; Conversion; Schemes; Alternatives; Preview; Shades and Tints; Tones; Blindness Simulator; In a RGB color space, hex #5b3914 is … bing search images by imageWebDescription: INCB053914, also known as Uzansertib, is a novel, potent, and selective adenosine triphosphate-competitive pan-PIM kinase inhibitor. In vitro, INCB053914 inhibited proliferation and the phosphorylation of downstream substrates in cell lines from multiple hematologic malignancies. da baby and his girlfriendWebFeb 25, 2024 · The study will be conducted in 4 parts. Part 1 (monotherapy dose escalation) will evaluate safety and determine the maximum tolerated dose of INCB053914 monotherapy and the recommended phase 2 dose(s) (a tolerated pharmacologically active dose that will be taken forward into the remaining parts of the study). da baby and latruth