Immunome says FDA clears IND for IM-1340 solid tumor ADC
- FDA cleared Immunome’s IND for IM-1340, a first-in-class antibody-drug conjugate for advanced solid tumors.
- Phase 1 trial is slated to start in Q4 2026 to assess safety, pharmacokinetics, and early anti-tumor activity.
- IM-1340 uses Immunome’s proprietary HC74 topoisomerase I inhibitor payload.
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