Morgan Stanley 24th Annual Global Healthcare Conference
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IDEAYA Biosciences (IDYA) Morgan Stanley 24th Annual Global Healthcare Conference summary

Event summary combining transcript, slides, and related documents.

Logotype for IDEAYA Biosciences Inc

Morgan Stanley 24th Annual Global Healthcare Conference summary

14 Sep, 2026

Pipeline overview and strategic focus

  • Precision medicine oncology pipeline includes lead agent darovasertib, DLL3 ADC, and MTAP deletion programs.

  • Darovasertib is nearing NDA submission under RTOR, with a projected launch in the first half of next year and multiple phase III studies ongoing.

  • DLL3 ADC program is advancing to a randomized phase III study in small cell lung cancer, with additional opportunities in neuroendocrine carcinoma.

  • Two collaborations with Roche focus on pan-RAS and KRAS G12D inhibitors in pancreatic cancer.

  • Additional assets include KAT6/7, CDKN2A, and PRMT5 programs targeting various solid tumors.

Darovasertib clinical and regulatory progress

  • NDA submission for darovasertib is nearly complete, with label strategy discussions ongoing; FDA is receptive to an all-comers approach.

  • Darovasertib shows a confirmed response rate near 40%, PFS of about 7 months, and OS over 21 months, outperforming current therapies.

  • Oral administration offers convenience over existing weekly IV treatments.

  • Commercial launch preparations include physician education, patient identification, and leveraging KOL networks and technology.

  • Phase III adjuvant study is underway, targeting relapse prevention with a well-powered design of 450 patients.

DLL3 ADC and combination strategies

  • DLL3 ADC aims for best-in-class status by balancing efficacy and safety, targeting higher response rates and improved PFS compared to competitors.

  • Upcoming ESMO presentation will provide data on response rate, PFS, and 12-month OS for about 100 patients.

  • Phase III study will focus on post-Imdelltra population in small cell lung cancer; registrational study in neuroendocrine carcinoma is under FDA discussion.

  • Combination strategies include novel PARG (IDE161) and PD-L1, with go/no-go decisions expected by end of next year.

  • PARG/IDE161 combinations aim to enhance durability and could be applied across topoisomerase-based therapies.

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