IDEAYA Biosciences Interim IDE397 Phase 1 Clinical Data and Q1 2022 Corporate Update slide image

IDEAYA Biosciences Interim IDE397 Phase 1 Clinical Data and Q1 2022 Corporate Update

IDE397 Clinical Pharmacokinetic Data Exposures are Dose Proportional and Achieved Active Exposure Targets # IDE397 Pharmacokinetic (PK) Data IDE397 PK Parameters at Steady State Plasma IDE397 Conc. 1 100x 10x 1x 0 8 16 24 Hours post-dose 1 Y-axis concentration scale discloses relative values as indicated Cycle 1 Day 15 Cohort 5 Cycle 1 Day 15 Cohort Cohort Cohort Cohort Cohort 1 2 3 4 5 Стах 1 1.0 x 3.6 x 4.3 x 12.0 x 17.5 x max Cohort 4 AUC 24h¹ 1.0 x 4.0 x 4.9 x 13.6 x 19.8 x -Cohort 3 max 1 C. and AUC 24h values normalized to Cohort 1 -Cohort 2 -Cohort 1 Target efficacious exposure range based on in vivo preclinical models - - IDE397 PK Profile Flat temporal PK profiles, with low Cmax/Cmin ratio Dose-proportional increase in exposures (AUC and Cmax) Cohort 1 to 5 Achieved target efficacious exposure range of in vivo preclinical models PK properties support acceptable dosing regimen Cohort 5 cleared without observing MTD 6 IDEAYA Data #Based on preclinical PK/PD analysis Currently enrolling Cohort 6; first patient cleared without DLT gsk IDEA A BIOSCIENCES
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