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Publications

ADC+DDR Combos

Combining targeted DNA damage with repair pathway inhibition to create synthetic lethality in cancer cells.

IDE034

Source

AACR 2026 Munoz et al.

IDE034, a bispecific antibody-drug conjugate co-targeting PTK7 and B7-H3, exhibits avidity-driven selectivity and enhanced antitumor activity versus monospecific ADCs

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IDE849

Source

ESMO 2026 Liu et al.

SHR-4849 (IDE849), an ADC targeting delta-like ligand 3 (DLL3), in relapsed small cell lung carcinoma (SCLC) and other neuroendocrine carcinomas (NECs): long-term results from the Phase 1 study

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IDE161

Source

IASLC WCLC 2025 Maskey et al.

Dual PARG-TOP1 inhibition exacerbates DNA-protein crosslinks and replication stress: A promising strategy for enhancing Top1i-ADC efficacy

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IDE161

Source

EORTC-NCI-AACR 2024 Munoz et al.

IDE161, a potential first-in-class clinical candidate PARG inhibitor, selectively targets solid tumors with replication stress and DNA repair vulnerabilities

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MTAP Pathway

Exploiting the dual metabolic vulnerabilities created by MTAP loss through a differentiated combination approach designed to drive deep and durable tumor responses.

IDE397 and IDE892

Source

AACR 2026 Rao et al.

IDE892 is a highly potent and selective PRMT5 inhibitor, with MTA-positive and SAM-negative cooperativity, optimized for development in MTAP-deleted cancers in combination with the allosteric MAT2A inhibitor IDE397

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IDE397 and IDE892

Source

AACR 2025 Aubi et al.

The impact of metabolite kinetics on dysregulation of essential enzymes in cancers with MTAP deficiencies

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IDE397 and IDE892

Source

EORTC-NCI-AACR 2024 Garbett et al.

The mechanistic basis of both deep and durable antitumor activity by combinatorial inhibition of MAT2A and PRMT5 in MTAP-deleted tumors

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