Rezubio Reports First Cohort Dosing in P-I Trial of RZ-520 Following FDA and NMPA IND Clearances

Shots:

• Rezubio has completed dosing of the first cohort in its P-I trial of RZ-520, following US FDA & Chinese NMPA clearances to assess its safety, tolerability, PK & PD in healthy volunteers
• RZ-520 is a clinical-stage asset developed using Rezubio’s MADD platform, with preclinical studies showing robust efficacy, superior safety & negligible systemic exposure across multiple disease models
• MADD platform engineers tissue-targeted therapies with prolonged local residence & optimized PK, enabling differentiated treatments against cell-surface proteins in the respiratory and GI tracts

Ref: Globenewswire | Image: Rezubio  |  Press Release

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