SMART-101 is under clinical development by Smart Immune 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 SMART-101’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.

SMART-101 overview

SMART-101 is under development for the treatment of acute lymphocytic leukemia, acute myeloid leukemia, relapsed/refractory acute myeloid leukemia, myelodysplastic syndrome and for use in hematopoietic stem cell transplantation. The therapeutic candidate is developed based on ex vivo thymus platform that differentiates CD34 positive stem cells purified from cord blood or peripheral hematopoietic stem cells into T Cell Progenitors so-called ProTcell. It is administered through parenteral route.

Smart Immune overview

Smart Immune is a company dedicated to the development of T-cell progenitor-based cell and gene therapy to combat blood cancers and infections. Smart Immune is headquartered in Paris, Ile-de-France, France.

For a complete picture of SMART-101’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 10 June 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.