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Investor Presentaiton

MAT2Ai Combination Strategy AMGEN® Clinical Combination focus on IDE397 + PRMT5MTA based on Compelling Preclinical Efficacy IDE397 + MTA-Cooperative PRMT5 Inhibitor enables Maximal Pathway Suppression* Maximal Pathway Suppression Methionine Hit 2 MAT2A IDE397 Deep and Durable Anti-Tumor and PD Response with Combination* PRMT5MTA-1 NSCLC MTAP (-/-) CDX -O- Vehicle IDE397 3 mg/kg IDE397 30 mg/kg 2000- PRMT5MTA-125 mg/kg PRMT5MTA-1 100 mg/kg IDE397 3 mg/kg + PRMT5MTA-1 25 mg/kg PRMT5MTA-1 Pancreatic MTAP (-/-) CDX PRMT5MTA-1 25 mg/kg -- Vehicle ▲ IDE397 3 mg/kg IDE397 3 mg/kg + PRMT5MTA-1 25 mg/kg 1500- MTA Hit 1 MTA PRMT5 MTAP MTA Hit 3 PRMT5MTA MTA SAM Methylation of Splicing Factors (SDMA) In Vivo Efficacy Confirmed in Multiple Models Pre-mRNA Splicing (Essential) Enhanced Combination Efficacy Observed in multiple Tumor Indications and Across Representative PRMT5MTA Inhibitors + Mean Tumor Volume (mm³) ± S.E.M. 1500- 1000- 500- 0+ ō 0 10 20 30 40 50 60 Study Day Mean Tumor Volume (mm³) ± S.E.M. 1000- 500- 0- 10 20 30 40 50 60 Study Day MTAP-deleted Tumor SDMA IHC Scores PRMT5MTA-2 NSCLC MTAP (-/-) CDX -- Vehicle 100% PRMT5MTA-2 30 mg/kg IDE397 3 mg/kg + 75%- ✰IDE397 3 mg/kg PRMT5MTA-2 30 mg/kg 2000- 50%- 1500- 25%- Mean Tumor Volume (mm³) ± S.E.M. 1000- 500- IDE397 Vehicle 3 mg/kg ☐ ☐ ☐ ☐ 3+ 2+ 1+ 0 25 * Clinical evaluation pursuant to Amgen Clinical Trial Collaboration and Supply Agreement for clinical evaluation of IDE397 and AMG 193, an Amgen investigational MTA-cooperative PRMT5 inhibitor; Amgen will sponsor the study; IDEAYA and Amgen will jointly share external costs of the study T 0 10 20 30 40 50 60 Study Day SDMA IHC nuclear staining intensity distribution, pathologist scored, as percent of total tumor cells evaluated per sample; tumor samples from HCT116 MTAP (-/-) CDX models collected 2 hrs post-dose on Treatment Day 2 + IDEAYA Data: AACR 2023, M. Fischer et al. based on evaluation of multiple representative MTA-cooperative PRMT5 inhibitors, designated as PRMT5MTA-1, PRMT5MTA-2 IDEA A BIOSCIENCES PRMT5¡MTA IDE397 + PRMT5iMTA
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