CKBO-5102 is under clinical development by CK Regeon and currently in Phase I for Bone Disorders. According to GlobalData, Phase I drugs for Bone Disorders have a 66% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how CKBO-5102’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.

CKBO-5102 overview

CKBO-5102 is under development for the treatment of short stature. It is administered by the oral route. The drug candidate acts by targeting CXXC-type zinc finger protein 5 (CXXC5). It is a new chemical entity.

CK Regeon overview

CK Biotech Inc., is a biotechnology company that discover and develop First-In-?Class drugs with clear MOA. The company is headquartered Republic of Korea (South Korea).

For a complete picture of CKBO-5102’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 2 September 2023

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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.