CB-0135 is under clinical development by Cosmo Pharmaceuticals and currently in Phase II for Proctitis. According to GlobalData, Phase II drugs for Proctitis have a 67% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how CB-0135’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.
CB-0135 overview
Rifamycin (CB-01-35) is under development for the treatment of distal ulcerative colitis and proctitis. The drug candidate acts by targeting DNA directed RNA polymerase subunit beta and is administered by rectal route in the form of enema.
Cosmo Pharmaceuticals overview
Cosmo Pharmaceuticals (Cosmo) develops drugs for the treatment of gastrointestinal diseases and dermatology. It develops pharmaceutical products based on its multi-matrix technology. The company offers products such as Lialda, Mezavant, Mesavancol and Uceris for the treatment of ulcerative colitis. It also offers Eleview which is a submucosal injectable composition for use in gastrointestinal endoscopic procedures. The company’s manufacturing facility is located in Lainate, Milan. Cosmo is headquartered in Dublin, Ireland.
For a complete picture of CB-0135’s drug-specific PTSR and LoA scores, buy the report here.
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