AGA-2115 is under clinical development by Angitia Biopharmaceuticals and currently in Phase I for Osteogenesis Imperfecta. According to GlobalData, Phase I drugs for Osteogenesis Imperfecta have a 100% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how AGA-2115’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.

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.

AGA-2115 overview

AGA-2115 is under development for the treatment of osteogenesis imperfecta (OI). It is a bi-specific monoclonal antibody which acts by targeting sclerostin and dickkopf-1 related protein 1 (DKK1). It is administered through subcutaneous and intravenous route.

Angitia Biopharmaceuticals overview

Angitia Biopharmaceuticals engages in the development of new drugs for the treatment of skeletal, muscle, joint, and other diseases. The company is headquartered in Guangzhou, Guangdong, China.

For a complete picture of AGA-2115’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 10 June 2024

Data Insights


The gold standard of business intelligence.

Blending expert knowledge with cutting-edge technology, GlobalData’s unrivalled proprietary data will enable you to decode what’s happening in your market. You can make better informed decisions and gain a future-proof advantage over your competitors.


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.