biologic

Kisunla

donanemab-azbt

Loss of exclusivityJuly 2036projected — 12-year biologic exclusivity estimate
CompanyEli Lilly and Company

Drug detail

Brand nameKisunla
Active ingredientdonanemab-azbt
Strength350MG/20ML (17.5MG/ML)
Dosage formInjection
RouteIntravenous
ModalityBiologic
FDA approvalJuly 2024
Marketing statusRx

Source: FDA Purple Book, layered on the CliffBio company graph. Cliff dates are the projected — 12-year biologic exclusivity estimate; estimates are projections, not legal advice.

Kisunla patent cliff — loss of exclusivity July 2036 | CliffBio