NMDP-02 is under clinical development by NMD Pharma and currently in Phase II for Spinal Muscular Atrophy (SMA). According to GlobalData, Phase II drugs for Spinal Muscular Atrophy (SMA) have a 71% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how NMDP-02’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.
NMDP-02 overview
NMDP-02 is under development for the treatment of spinal muscular atrophy type 3. It acts by targeting chloride channel protein 1 (CLC-1). It is administered through oral route.
For a complete picture of NMDP-02’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.
