SIR-9900 is under clinical development by Sironax and currently in Phase I for Inflammation. According to GlobalData, Phase I drugs for Inflammation have a 44% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how SIR-9900’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.

SIR-9900 overview

SIR-9900 is under development for the treatment of inflammatory diseases, particularly in central nervous system and degenerative diseases, particularly in central nervous system. It acts by targeting receptor interacting serine/threonine protein kinase 1 (RIP1). It is administered through oral route.

Sironax overview

Sironax is a pharmaceuticals and healthcare company discovering transformational therapies to degenerative disease patients. The company is headquartered in Beijing City, Beijing, China.

For a complete picture of SIR-9900’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.