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The company’s sole internal clinical asset is micvotabart pelidotin, an antibody-drug conjugate licensed from Pfizer. Phase 1 dose-escalation results in solid tumors showed encouraging safety and tolerability. No objective responses were reported for the discontinued monoclonal antibody PYX‑106 targeting Siglec‑15. The company is launching expansion trials of its ADC as monotherapy and in combination with pembrolizumab ("Keytruda") in head and neck squamous cell carcinoma, HR+/HER2– breast cancer, and triple-negative breast cancer.
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