VGB-Ex01 is under clinical development by Shanghai Vitalgen BioPharma and currently in Phase II for Beta Thalassaemia. According to GlobalData, Phase II drugs for Beta Thalassaemia have a 38% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how VGB-Ex01’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.

VGB-Ex01 overview

VGB-Ex01 is under development for the treatment of beta-thalassemia. The therapeutic candidate comprises of CRISPR-Cas12b, HBG1/2 promoter edited autologous hematopoietic stem cells. It is administered through parenteral route.

Shanghai Vitalgen BioPharma overview

Shanghai Vitalgen BioPharma (Vitalgen BioPharma) operates in healthcare sector. Vitalgen BioPharma is headquartered in Shanghai,China.

For a complete picture of VGB-Ex01’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 7 February 2024

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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.