CCX-507 is under clinical development by Amgen and currently in the Phase I in clinical pathway. The characteristics of the clinical trial as well as other attributes related to the drug, regulations, and company play a fundamental role in ensuring the likelihood of transition that the drug moves from its current development stage to next.
According to GlobalData, the latest event to affect CCX-507’s likelihood of approval (LoA) and phase transition for Crohn’s Disease (Regional Enteritis) took place on 24 Oct 2022, which increased the likelihood that the drug progresses to the next phase in its clinical pathway and increased the likelihood of final approval for this indication.
GlobalData uses proprietary data and analytics to provide a complete picture of this assessment in their CCX-507 Likelihood of Approval (LoA) and Phase Transition Success Rate (PTSR) Report.
CCX-507 is under development for the treatment of inflammatory bowel diseases (IBD) including ulcerative colitis and Crohn's disease (CD). The drug candidate is a small molecule and administered orally. CCX-507 is a second generation CCR9 inhibitor. It is developed based on EnabaLink platform. It was also under development for the treatment of primary sclerosing cholangitis (PSC).
Amgen is a biotechnology company, which discovers, develops, manufactures, and markets innovative human medicines to treat patients suffering from serious diseases. It develops novel medicines in six focused disease areas including cardiovascular diseases, oncology/hematology, inflammation, bone health, neurological disorders and nephrology. The company develops products using advanced human genetics to unravel the difficulties of disease and understand the fundamentals of human biology. Amgen sells products primarily to pharmaceutical wholesale distributors in the US. It also markets certain products directly to consumers through direct-to-consumer channels such as print, television and online media. Amgen is headquartered in Thousand Oaks, California, the US.
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