QBECO is under clinical development by Qu Biologics and currently in Phase I for Ovarian Cancer. According to GlobalData, Phase I drugs for Ovarian Cancer have a 73% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how QBECO’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.
QBECO overview
QBECO-SSI is under development for the treatment of colon cancer, liver cancer, pancreatic cancer, metastatic colorectal cancer, ovarian cancer, Crohn's disease and ulcerative colitis. The drug candidate is administered through subcutaneous route. It acts as cell modulator and immuno-modulator. The drug candidate is based on site specific immunotherapy (SSIs) technology. QBECOSSI, derived from components of inactivated E. coli.
Qu Biologics overview
Qu Biologics is a biotechnology company that discovers and develops immunotherapies for the treatment of cancer and other immune-related diseases. It utilizes its site-specific immunomodulators (SSI), a novel proprietary immunotherapy platform to restore normal immune function in the targeted tissue to reverse chronic inflammation in diseases including cancer, inflammatory bowel disease, and other immune-related conditions. Its therapies are also used to treat lung cancer, gastric, kidney, and prostate cancer, ovarian cancer, bone cancer, ulcerative colitis, and arthritis. Qu Biologics also offers preclinical research, retrospective studies, compassionate use program, and clinical trial programs. The company works in collaboration with pharmaceutical companies and academic institutions to develop its products. Qu Biologics is headquartered in Burnaby, British Columbia, Canada.
For a complete picture of QBECO’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.
