TNX-1900 is under clinical development by Tonix Pharmaceuticals Holding and currently in Phase II for Obesity. According to GlobalData, Phase II drugs for Obesity have a 29% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how TNX-1900’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
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TNX-1900 overview
Oxytocin (TI-001) is under development for the treatment of binge eating disorder, social anxiety disorder (SAD), obesity in adults and pediatrics and autism spectrum disorder (ASD). The drug candidate is an intranasal oxytocin formulation. It acts by targeting oxytocin receptor and CGRP (Calcitonin Gene Related Peptide) . It was also under development for the treatment of trigeminal neuralgia, chronic daily headache (CDH), craniofacial pain, mild traumatic brain injury, binge eating disorder, insulin resistance and obesity.
It was also under development for the treatment of chronic migraine.
Tonix Pharmaceuticals Holding overview
Tonix Pharmaceuticals Holding (Tonix) a developer of pharmaceutical products to address public health challenges. The company offers pharmaceutical products and treatments for disorders of the central nervous system including fibromyalgia, post-traumatic stress disorder and episodic tension-type headache. Its products include Central Nervous System Portfolio; TNX-102 SL, TNX-1300, TNX-1900, Immunology Portfolio; TNX-1500(Organ Transplant Rejection / Autoimmune Disorders), TNX-1850 COVID-19 Vaccine and Rare Disease Portfolio; TNX-2900 (Prader-Willi Syndrome). Its disintegrating sublingual tablets contain a dose and formulation of cyclobenzaprine and are used for the treatment of fibromyalgia and post-traumatic stress disorder. It markets its products through a network of distributors across the US. It has operations in Ireland, Canada and the US. Tonix is headquartered in New York, the US
For a complete picture of TNX-1900’s drug-specific PTSR and LoA scores, buy the report here.
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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.
