SBT-101 is under clinical development by SwanBio Therapeutics and currently in Phase II for Adrenomyeloneuropathy (AMN). According to GlobalData, Phase II drugs for Adrenomyeloneuropathy (AMN) does not have sufficient historical data to build an indication benchmark PTSR for Phase II. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the SBT-101 LoA Report. 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.

SBT-101 overview

SBT-101 is under development for the treatment of adrenomyeloneuropathy (AMN). It is an adeno associated virus (AAV) based gene therapy. It is administered through intrathecal route. It was under development for neurodegenerative diseases.

SwanBio Therapeutics overview

SwanBio Therapeutics is a gene therapy company which is advancing AAV-based therapies to treat inherited neurological conditions. The company is headquartered in Bala Cynwyd, Pennsylvania, the US.

For a complete picture of SBT-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.