CyPep-1 is under clinical development by Cytovation and currently in Phase II for Liver Cancer. According to GlobalData, Phase II drugs for Liver Cancer have a 31% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how CyPep-1’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
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CyPep-1 overview
CyPep-1 is under development for the treatment of cutaneous warts (papillomas) caused by human papilloma virus, metastatic melanoma, nasopharyngeal squamous cell carcinoma, head and neck squamous cell carcinoma (HNSCC) and triple-negative breast cancer (TNBC), recurrent respiratory papillomatosis (RRP), adrenocortical carcinoma, colorectal cancer, hepatocellular carcinoma and liver cancer. It is administered topically as cream for warts and intratumorally and subcutaneous for solid tumors and lymphoma. CyPep-1 is a tumor specific, cytotoxic peptide with extreme lipid penetrating properties. CyPep-1 targets the wart cells and induces rapid necrotic cell death. The drug candidate was also under development for the treatment of multi-resistant bacterial infections such as E.coli infections and skin cancer.
Cytovation overview
Cytovation is a biotech company that develops novel therapeutic agents for skin diseases and infections. The company’s lead candidate includes CyPep-1, a novel peptide and an anti-bacterial compound. Its CyPep-1 is developed for skin disorders such as papilloma diseases, tumors of skin warts caused from HPV transfected transformed keratinocytes and cypep-1 selectivly targets and lyses skin tumor cells due to negative chargeon cell membrenes. Cytovation targets the wart cells and destroys the transformed cancer cells and a wide range of drug resistant bacterias such as E-coli bacterias. The company partners with pharmaceutical companies, scientific institutions and research organizations. Cytovation is headquartered in Bergen, Norway.
For a complete picture of CyPep-1’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.
