INK Acute Myeloid Leukemia is under clinical development by Nuwacell Biotechnology and currently in Phase II for Acute Myelocytic Leukemia (AML, Acute Myeloblastic Leukemia). According to GlobalData, Phase II drugs for Acute Myelocytic Leukemia (AML, Acute Myeloblastic Leukemia) have a 30% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how INK Acute Myeloid Leukemia’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.

INK Acute Myeloid Leukemia overview

The therapeutic candidate is under development for the treatment of acute myeloid leukemia. It comprises of natural killer (NK) cells derived from induced pluripotent stem cells (iPSCs).

Nuwacell Biotechnology overview

Nuwacell Biotechnology focuses on stem cell research and product development. Nuwacell Biotechnology is headquartered in Hefei, Anhui, China.

For a complete picture of INK Acute Myeloid Leukemia’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.