Disclosures: Peyton Classon: Nothing to Disclose, Sophia Jaramillo: Nothing to Disclose, Danielle Carlson: Nothing to Disclose, Irene Yan: Nothing to Disclose, Sumera Ilyas: Astrazeneca: Consultant, Rory Smoot: Nothing to Disclose, Gregory Gores: Nothing to Disclose, Tushar Patel: Nothing to Disclose, Davide Povero: Nothing to Disclose 1831 T CELL RECEPTOR AND IMMUNE GENE EXPRESSION PHARMACODYNAMICS FOR DURVALUMAB MONOTHERAPY AND IN COMBINATION WITH TREMELIMUMAB OR BEVACIZUMAB IN UNRESECTABLE HEPATOCELLULAR CARCINOMA (UHCC) Robin Kate Kelley 1 Young Lee 2 James Conway 2 John Kurland 2 Alejandra Negro 2 Patricia McCoon 3 , 1 Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA, USA, 2 Oncology R&D, AstraZeneca, Gaithersburg, MD, USA, 3 Oncology R&D, AstraZeneca, Waltham, MA, USA Background: Study 22 (NCT02519348), a Phase 2 trial of immune checkpoint inhibitor (ICI) monotherapy and combination regimens in uHCC, showed higher rates of objective response (ORR) with STRIDE (Single Tremelimumab [T] Regular Interval Durvalumab [D]) or D+bevacizumab (B) than with D

References 1.Bauman D, Baumgard L, Corl B, Griinari JM
Of the 6 myo-inositol mQTLs identified, all had been previously associated with higher myo-inositol levels based on review of the GWAS catalog
Monthly supply capabilities of 50 kg from specialized makers like Xi'an Yihui show that production processes and networks for getting raw materials are well-established