SIS-302AA is under clinical development by Sisaf and currently in Phase II for Alopecia Areata. According to GlobalData, Phase II drugs for Alopecia Areata have a 48% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how SIS-302AA’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.
SIS-302AA overview
SIS-302-AA is under development for the treatment of autoimmune alopecia. The therapeutic candidate is administered through topical route and is being developed based on Bio-Courier technology.
Sisaf overview
Sisaf is a biopharmaceutical company that develops ribonucleic acid (RNA) therapeutics for rare diseases. The company develops therapeutics using bio-courier and ribonucleic acid (RNA) delivery technologies. Its pipeline products include SIS-101-ADO treats autosomal dominant osteopetrosis; SIS-102-ACH targets achondroplasia; SIS-401-PACA for solid tumors and pancreatic cancer; SIS-402-SBC treats secondary cancer. Its partnered pipeline products include SIS-302-AA treats alopecia; SIS-201-CD and SIS-202-CDC, which targets Type II Corneal Dystrophy. Sisaf is headquartered in Belfast, the UK.
For a complete picture of SIS-302AA’s drug-specific PTSR and LoA scores, buy the report here.
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