Botulinum toxin is under clinical development by Huons and currently in Phase III for Upper Limb Muscle Spasticity. According to GlobalData, Phase III drugs for Upper Limb Muscle Spasticity have a 100% phase transition success rate (PTSR) indication benchmark for progressing into Pre-Registration. GlobalData’s report assesses how Botulinum toxin’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.
Botulinum toxin overview
Botulinum toxin is under development for the treatment of post stroke upper limb spasticity disorders and benign masseteric hypertrophy (unspecified musculoskeletal disorders). It is administered through intramuscular route. The drug candidate acts by targeting synaptosomal associated protein 25 (SNAP25).
Huons overview
Huons, a subsidiary of Huons Global Co Ltd, develops and provides various pharmaceuticals and medical devices. The company’s products include oral solid form, injection, medical devices, eye drop products and bioproducts, It also provides various products including the circulatory system, metabolic, antipyretic analgesic anti-inflammatory, urogenital system, musculoskeletal system, respiratory system product, antibiotic product, well-being product, urogenital system product, antihistamine and other chemotherapeutic products. Huons offers all its products under the brand Huons. The company operates in South Korea. Huons is headquartered in Gyeonggi-do, South Korea.
For a complete picture of Botulinum toxin’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.
