Roche to announce new data in rheumatoid arthritis and severe inflammatory disorders at the European League Against Rheumatism Annual Congress
“People with rheumatological conditions have relied on our medicines for more than a decade, and we are committed to developing treatments for other debilitating autoimmune diseases,” said Sandra Horning, M.D., Roche’s Head of Global Product Development and Chief Medical Officer. “We are proud to apply our insights into the biology of inflammation to conditions where patients have inadequate, or no currently approved, treatment options.”
Data to be presented at EULAR 2015 shows the depth and breadth of Roche in RA and other autoimmune diseases. Results from studies in early RA, SSc, systemic juvenile idiopathic arthritis (sJIA) – a severe form of arthritis affecting children – and rare conditions characterised by inflammation of blood vessels will be presented.
Overview of oral and poster presentations for Roche at EULAR. Please note the EULAR embargo date (10th June, 00:01 CET) for inclusion of information relating to the abstract (besides the abstract title, date and time).
| Presentation title | Abstract number / presentation timings (all times listed are Central European Time) |
|---|---|
| Rapid and sustained remission in early rheumatoid arthritis treated to target with tocilizumab, methotrexate, or their combination: the U-ACT-EARLY strategy study | ORAL (OP0033) Thursday, June 11. Session: 10:30-12:00PM Presentation Time: 11:15-11:25AM, Hall 8 |
| Safety and efficacy of subcutaneous (SC) tocilizumab (TCZ) in adults with systemic sclerosis (SSc): week 48 data from the FaSScinate trial | ORAL (OP0054) Thursday, June 11. Session: 10:30-12:00PM Presentation Time: 10:35-10:45AM, Hall 1 |
| Efficacy and safety of tocilizumab in patients with systemic juvenile idiopathic arthritis: 5-year data from TENDER, a phase 3 clinical trial | POSTER (THU0508) Thursday, June 11 12:00-1:45PM. Hall 5 |
| Tapering and withdrawal of tocilizumab in patients with systemic juvenile idiopathic arthritis in inactive disease: results from an alternative dosing regimen in the TENDER study | POSTER (SAT0483) Saturday, June 13 10:15-12:00PM. Hall 5 |
| A multicenter, open-label, long-term extension study of SUMMACTA and BREVACTA to evaluate safety and efficacy of tocilizumab SC in patients with moderate to severe RA | POSTER (SAT0180) Saturday, June 13 10:15-12:00PM. Hall 6 |
| The association between cumulative glucocorticoid exposure and glucocorticoid-related adverse events among patients with rheumatoid arthritis: a U.S. administrative claims database analysis | POSTER (SAT0344) Saturday, June 13 10:15-12:00PM. Hall 6 |
| Immunogenicity, safety and efficacy of subcutaneous tocilizumab in patients who missed doses | POSTER (FRI0153) Friday, June 12 12:05-1:45PM. Hall 6 |
| Characteristics of newly-diagnosed versus relapsing disease in GiACTA | POSTER (FRI0248) Friday, June 12 12:00-1:45PM. Hall 6 |
| Estimating the cost of illness of giant cell arteritis | POSTER (THU0347) Thursday, June 11 12:00-1:45PM. Hall 6 |
| Clinical and economic burden of patients with granulomatosis with polyangiitis (GPA) in the United States (health economics and outcomes research) | POSTER (FRI0267) Friday, June 12 12:00-1:45PM. Hall 6 |
| Clinical and economic burden of patients with microscopic polyangiitis (MPA) in the United States (health economics and outcomes research) | POSTER (THU0287) Thursday, June 11 12:00-1:45PM. Hall 6 |
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