KLS1.2-1 is under clinical development by Nomax Therapeutics and currently in Phase I for Parkinson’s Disease. According to GlobalData, Phase I drugs for Parkinson’s Disease have a 72% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how KLS1.2-1’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.

KLS1.2-1 overview

KLS1.2-1 is under development for the treatment of Parkinson's disease. KLS-1 is a zinc (Zn) aspartate enriched with light stable zinc isotope (64Zn) to 99.2 percent mass fraction of total zinc. The therapeutic candidate is administered as an intravenous (IV) infusion.

Nomax Therapeutics overview

Nomax Therapeutics is a developer of isotope-selective modulation therapies used for the treatment of neurological diseases including Parkinson’s disease, Alzheimer disease, dementia, multiple sclerosis, amyotrophic lateral sclerosis (ALS). The company is headquartered in Miami, Florida, the US.

For a complete picture of KLS1.2-1’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.