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Treatment of ulcerative colitis (UC) and Crohn’s disease (CD) within Brazil and Mexico includes many of the predominant treatments in other parts of the world such as the TNF-α inhibitors. Notably, however, treatment is driven by the reimbursement status within given markets that curtail reimbursement of some therapies (with variations between public and private settings). The potential arrival of several more agents offering novel MOAs and/or formulations (e.g., Pfizer’s tofacitinib, Gilead/Galapagos’ filgotinib, Roche/Genentech’s etrolizumab), as well as increasing physician experience with prescribing biosimilars, will fuel competition and pricing pressure in these markets. Emerging therapies seeking to maximize patient shares must address the pressure points that drive reimbursement decisions within the Brazilian and Mexican markets.
Questions Answered in This Report:
Decision Resources Group’s Access and Reimbursement module for Crohn’s disease and ulcerative colitis in Brazil and Mexico explores the prescribing patterns for current targeted therapies, the potential impact of the anticipated arrival of novel therapies, and key national and regional market access factors that will shape the use of targeted therapies over the next two to three years. This content draws on insights from 101 surveyed physicians and from interviews with 6 payers in Brazil and Mexico, all of whom have influence at the regional, institutional, or national level.
Markets covered: Brazil and Mexico
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