XT-150 is under clinical development by Xalud Therapeutics and currently in Phase II for Peripheral Neuropathic Pain. According to GlobalData, Phase II drugs for Peripheral Neuropathic Pain have a 19% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how XT-150’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.

XT-150 overview

XT-150 is under development for the treatment of peripheral neuropathic pain-lumbar radiculopathy, central neuropathic pain, multiple sclerosis, facet syndrome, osteoarthritis, osteoarthritis pain, amyotrophic lateral sclerosis, unspecified dermatological disorders and unspecified ophthalmological disorders. It is administered through the intraarticular and intrathecal route. The drug candidate is a non-viral vector-based gene therapy that comprises of a combination of plasmid DNA nucleic acid expressing IL-10 protein and a compound that improves the uptake of the plasmid into cells. It was also under development for the treatment of chemotherapy-induced peripheral neuropathy, thermal analgesia, degenerative disc disease and unspecified gastrointestinal disorders.

Xalud Therapeutics overview

Xalud Therapeutics is developing a paradigm in gene therapy delivery to address chronic inflammation. The company is headquartered in New York City, New York, the US.

For a complete picture of XT-150’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 12 April 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.