LPXTI-641 is under clinical development by Lapix Therapeutics and currently in Phase I for Multiple Sclerosis. According to GlobalData, Phase I drugs for Multiple Sclerosis have a 73% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how LPXTI-641’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.

LPXTI-641 overview

LPX-TI641 is under development for the treatment of multiple sclerosis (MS), neuromyelitis optica spectrum disorders (NMOSD), rheumatoid arthritis and myelin oligodendrocyte glycoprotein antibody disease (MOGAD). The drug candidate acts as T cell immunoglobulin and mucin domain-containing protein (TIM) 3/4 receptor agonist. The drug candidate is administered through oral route. 

Lapix Therapeutics overview

Lapix Therapeutics (Lapix) is a healthcare company that develops therapies to improve the immune system with modulations. Lapix is headquartered in Boston, Massachusetts, the US.

For a complete picture of LPXTI-641’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.