ORTHO-R is under clinical development by ChitogenX and currently in Phase II for Unspecified Musculoskeletal Disorders. According to GlobalData, Phase II drugs for Unspecified Musculoskeletal Disorders does not have sufficient historical data to build an indication benchmark PTSR for Phase II. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the ORTHO-R LoA Report. 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.
ORTHO-R overview
Ortho-R is under development for the treatment of rotator cuff tear repair, post meniscal repair. It is administered as implant. The therapeutic candidate is a combination product comprising freeze-dried chitosan and autologous platelet rich plasma (PRP).
ChitogenX overview
ChitogenX is an emerging orthobiologics company dedicated to the development of novel therapeutic tissue repair technologies to dramatically improve the success rate of orthopedic musculoskeletal surgeries. ChitogenX is headquartered in Kirkland, Quebec, Canada.
For a complete picture of ORTHO-R’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.
