Mesenchymal Stem Cell (MSC) is under clinical development by Cell Energy Life Sciences Group and currently in Phase II for Human Immunodeficiency Virus (HIV) Infections (AIDS). According to GlobalData, Phase II drugs for Human Immunodeficiency Virus (HIV) Infections (AIDS) have a 39% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Mesenchymal Stem Cell (MSC)’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.
Mesenchymal Stem Cell (MSC) overview
The are under development for the treatment of human immunodeficiency virus (HIV) infections (AIDS) and lung injury. The therapeutic candidate is administered through intravenous route.
Cell Energy Life Sciences Group overview
Cell Energy Life Sciences Group provides clinical trials by using mesenchymal stem cells to treat patients suffering with advanced stages of AIDS. The company is headquartered in Qingdao, Shandong, China.
For a complete picture of Mesenchymal Stem Cell (MSC)’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.
