Skip to main content
. Author manuscript; available in PMC: 2020 Aug 1.
Published in final edited form as: Mol Cancer Ther. 2019 Oct 8;19(2):397–408. doi: 10.1158/1535-7163.MCT-19-0319

Figure 4:

Figure 4:

Orally administered JHU395 has minimal GI or hepatotoxicity. A) Average weight change in flank MPNST mice treated during efficacy study with vehicle or JHU395 (1.2 mg/kg/day p.o. × 5 days, then 0.5 mg/kg p.o. × 9 days; n=9). Change from mean starting weight did not exceed 10%. B) Jejunal histology in a subset of vehicle and JHU395 treated mice after 14 days oral dosing. No increase in apoptotic figures or disruption of crypt architecture was observed. Scalebar = 49 μm. C) Markers of liver toxicity from blood (AST, ALT, total bilirubin) were measured in vehicle or JHU395 treated animals at sacrifice (day 15). All data shown is mean +/− S.D. p > 0.05 for each lab value by t-test.