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(b) LithoVue TM Elite Digital Flexible Ureteroscope System With Pressure Monitoring Boston Scientific Corporation submitted an application for a new device category for transitional pass-through payment status for the LithoVue TM Elite Digital Flexible Ureteroscope System with Pressure Monitoring (the LithoVue TM Elite System) for CY 2026

The splitting revealed an HR of 0.87 (95%CI 0.541.40) and HR of 0.93 (95% CI 0.581.48), respectively

In vitro and ex vivo studies have shown that CD38 expression levels correlate with isatuximab- and daratumumab-induced ADCC and CDC [78]

S2CID 16101442

Informed consent: The healthcare provider must document that the patient received and understood the information about the Depo-Provera injection and provided informed consent for the treatment