AGA-2118 is under clinical development by Angitia Biopharmaceuticals and currently in Phase II for Post Menopausal Osteoporosis. According to GlobalData, Phase II drugs for Post Menopausal Osteoporosis have a 77% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how AGA-2118’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-2118 overview

AGA-2118 is under development for the treatment of osteoporosis and postmenopausal women osteoporosis. It comprises of bispecific antibody. It is administered intravenously or subcutaneously. It acts by targeting Sclerostin and DKK1.

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-2118’s drug-specific PTSR and LoA scores, buy the report here.

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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.