Donanemab is under clinical development by Eli Lilly and Co and currently in Pre-Registration for Alzheimer’s Disease. According to GlobalData, Pre-Registration drugs for Alzheimer’s Disease have a 50% phase transition success rate (PTSR) indication benchmark for progressing into Marketed. GlobalData’s report assesses how Donanemab’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.

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GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.

Donanemab overview

Donanemab (LY-3002813) is under development for the treatment of early symptomatic Alzheimer's disease. It is administered intravenously and subcutaneously. LY-3002813 is a monoclonal antibody that acts by targeting N3pG beta-amyloid (amyloid precursor protein). The drug candidate is a new biological entity (NBE).

For a complete picture of Donanemab’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 10 June 2024

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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.

GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.