TLSG-1 is under clinical development by InnoMedica and currently in Phase I for Parkinson’s Disease. According to GlobalData, Phase I drugs for Parkinson’s Disease have a 72% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how TLSG-1’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.
TLSG-1 overview
TLSG-1 is under development for the treatment of Huntington’s disease, Parkinson’s disease and Amyotrophic Lateral Sclerosis. The drug candidate is a liposomal GM1 developed based on liposomal targeting technology that involves encapsulation of the drug candidate in a liposome. It is administered through oral and intravenous route.
InnoMedica overview
InnoMedica discovers and develops therapeutics for the treatment of cancer. The company develops drugs using its proprietary drug delivery technology, Talidox, based on the transport and release of active pharmaceutical agent, locally, at the target area. Its pipeline portfolio includes targeted liposomal doxorubicin TLD-1/Talidox for the treatment of advanced metastatic tumors. The company’s pipeline portfolio also includes other candidates for the therapeutic areas of autoimmune diseases such as multiple sclerosis, arteriosclerosis and chronic inflammatory diseases. It operates through a office and production facility in Bern and Marly located in Switzerland, respectively. InnoMedica is headquartered in Zug, Switzerland.
For a complete picture of TLSG-1’s drug-specific PTSR and LoA scores, buy the report here.
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