- 15 oral presentations from 17 abstracts across six autoimmune conditions
- First presentation of Actemra/RoActemra data from GiACTA – the largest ever clinical trial in people with giant cell arteritis (GCA), a condition for which there has been no approved therapy in more than 50 years
- New data from two studies investigating cardiovascular outcomes for people with rheumatoid arthritis (RA) treated with Actemra/RoActemra
BASEL, 07-Nov-2016 — /EuropaWire/ — Roche (SIX: RO, ROG; OTCQX: RHHBY) today announced that new data from Actemra®/RoActemra® and Rituxan®/MabThera® will be presented during the 2016 American College of Rheumatology (ACR) and Association for Rheumatology Health Professionals (ARHP) Annual Meeting from 11-16 November in Washington, D.C, US. These data add to the significant body of evidence for Actemra®/RoActemra® and Rituxan®/MabThera® in RA and other serious immune-mediated conditions including GCA, systemic sclerosis (SSc), Takayasu arteritis, granulomatosis with polyangiitis (GPA) and microscopic polyangiitis (MPA).
“Advances in our scientific understanding of immune pathways are guiding the development of potential new treatments for severe autoimmune conditions,” said Sandra Horning, MD, Roche’s Chief Medical Officer and Head of Global Product Development. “Building on our more than a decade of experience in providing treatment options for people suffering from rheumatologic conditions, we look forward to sharing new data at this year’s ACR/ARHP meeting.”
At this meeting, key presentations from Roche will include: the first efficacy and safety results from GiACTA – a study investigating Actemra/RoActemra in GCA, an often chronic, potentially life-threatening autoimmune condition; ENTRACTE, a Phase IV study in patients with RA evaluating the risk of cardiovascular (CV) events with Actemra/RoActemra in comparison to etanercept; a real world data analysis of CV outcomes in RA patients who switched from another biologic agent to either Actemra/RoActemra or a tumour necrosis factor inhibitor (TNFi); plus further insights into the use of Actemra/RoActemra in SSc. Additionally, treatment insights from Rituxan/MabThera in RA and GPA/MPA will also be presented.
Overview of key oral and poster presentations featuring Roche medicines at the 2016 ACR/ARHP Annual Meeting. Please note that in accordance with the meeting’s policy, all abstract data is strictly embargoed until 12 November 2016, 4.30 PM ET.
Presentation title | Abstract number / presentation timings
(all times listed are Eastern Standard Time) |
Tocilizumab studies | |
Efficacy and Safety of Tocilizumab in Patients with Giant Cell Arteritis: Primary and Secondary Outcomes from a Phase 3, Randomised, Double-Blind, Placebo-Controlled Trial
(Stone J, et al.) |
Type: Oral presentation
Abstract ID: 911 Sun, 13 November 11.00 AM – 12.30 PM |
Safety and Efficacy of Subcutaneous Tocilizumab in Early Systemic Sclerosis: Results from the Open-Label Period of a Phase 2 Randomised, Controlled Trial
(Khanna D, et al.) |
Type: Oral presentation
Abstract ID: 969 Sun, 13 November 02.30 – 04.00 PM |
Comparative Cardiovascular Safety of Tocilizumab Vs Etanercept in Rheumatoid Arthritis: Results of a Randomised, Parallel-Group, Multicentre, Noninferiority, Phase 4 Clinical Trial
(Giles JT, et al.) |
Type: Oral presentation
Abstract ID: 3L Tues, 15 November 04.30 – 06.00 PM |
Efficacy and Safety of Tocilizumab in Patients with Refractory Takayasu Arteritis: Results from a Randomised, Double-Blind, Placebo-Controlled, Phase 3 Trial in Japan
(Nakaoka Y, et al.) |
Type: Oral presentation
Abstract ID: 976 02.30 – 04.00 PM |
Comparative Effectiveness of Tocilizumab Monotherapy with Tumour Necrosis Factor Inhibitors in Combination with Methotrexate in Patients with Rheumatoid Arthritis and Prior Exposure to Tumour Necrosis Factor Inhibitors (Harrold L, et al.) | Type: Poster presentation
Abstract ID: 1596 Mon, 14 November 09.00 – 11.00 AM |
Cardiovascular Safety of Tocilizumab Versus Tumour Necrosis Factor Inhibitors in Patients with Rheumatoid Arthritis
(Kim SC, et al.) |
Type: Poster presentation
Abstract ID: 2611 Tue, 15 November 09.00 – 11.00 AM |
Methotrexate Adherence in an Online Network of Patients with Rheumatoid Arthritis
(Katic B, et al.) |
Type: Poster presentation
Abstract ID: 2532 Tue, 15 November 09.00 – 11.00 AM |
Patient-Reported Outcomes in Two Randomised, Controlled Trials (RCTs) in Patients with Rheumatoid Arthritis (RA) Treated with Tocilizumab (TCZ) Monotherapy Compared with Methotrexate (MTX) or Adalimumab (ADA)
(Strand V, et al.) |
Type: Poster presentation
Abstract ID: 2515 Tue, 15 November 09.00 – 11.00 AM |
Rituximab studies | |
Factors Associated with Glucocorticoid Exposure in ANCA-Associated Vasculitis
(Cascino MD, et al.) |
Type: Poster presentation
Abstract ID: 1930 Mon, 14 November 09.00 – 11.00 AM |
Clinical and Serologic Variables Associated with Renal Response Among Lupus Nephritis Phase III Trial Patients Treated with Standard of Care Immunosuppression
(Cascino MD, et al.) |
Type: Oral presentation
Abstract ID: 965 Sun, 13 November 2.30 – 4.00 PM |
Impact of Rituximab on Patient-Reported Outcomes in Patients With Rheumatoid Arthritis From the US Corrona Registry
(Harrold LR, et al.) |
Type: Poster presentation
Abstract ID: 1580 Mon, 14 November 09.00 – 11.00 AM |
Follow Roche on Twitter via @Roche. Keep up with ACR 2016 news and updates by following the event’s hashtag #ACR16.
About Roche in Immunology
The Roche Group’s immunology medicines include: Actemra®/RoActemra® (tocilizumab) for rheumatoid arthritis and juvenile idiopathic arthritis; Rituxan®/MabThera® (rituximab) for rheumatoid arthritis granulomatosis with polyangiitis and microscropic polyangiitis; Xolair® (omalizumab) in allergic asthma; Pulmozyme® (dornase alfa) for cystic fibrosis; and Esbriet® (pirfenidone) for idiopathic pulmonary fibrosis. Roche’s immunology pipeline includes: RG7625, a cathepsin S antagonist; RG6125, a monoclonal antibody targeting cadherin-11; RG7845 (GDC-0853), a novel Bruton’s tyrosine kinase (BTK) inhibitor; obinutuzumab for lupus nephritis and hypersensitised patients with end-stage renal disease; etrolizumab for ulcerative colitis and Crohn’s disease; and lebrikizumab in a number of respiratory conditions and atopic dermatitis.
Roche in Immunology:
http://www.roche.com/research_and_development/what_we_are_working_on/immunology.htm
About Roche
Roche is a global pioneer in pharmaceuticals and diagnostics focused on advancing science to improve people’s lives. Roche is the world’s largest biotech company, with truly differentiated medicines in oncology, immunology, infectious diseases, ophthalmology and diseases of the central nervous system. Roche is also the world leader in in vitro diagnostics and tissue-based cancer diagnostics, and a frontrunner in diabetes management. The combined strengths of pharmaceuticals and diagnostics under one roof have made Roche the leader in personalised healthcare – a strategy that aims to fit the right treatment to each patient in the best way possible.
Founded in 1896, Roche continues to search for better ways to prevent, diagnose and treat diseases and make a sustainable contribution to society. Twenty-nine medicines developed by Roche are included in the World Health Organization Model Lists of Essential Medicines, among them life-saving antibiotics, antimalarials and cancer medicines. Roche has been recognised as the Group Leader in sustainability within the Pharmaceuticals, Biotechnology & Life Sciences Industry eight years in a row by the Dow Jones Sustainability Indices.
The Roche Group, headquartered in Basel, Switzerland, is active in over 100 countries and in 2015 employed more than 91,700 people worldwide. In 2015, Roche invested CHF 9.3 billion in R&D and posted sales of CHF 48.1 billion. Genentech, in the United States, is a wholly owned member of the Roche Group. Roche is the majority shareholder in Chugai Pharmaceutical, Japan. For more information, please visit www.roche.com.
All trademarks used or mentioned in this release are protected by law.
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SOURCE: The Roche Group
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- Reporting of legal documents concluded by DIGI Communications N.V. in February 2020 or in other period but effective in February 2020, in accordance with article 82 of Law no. 24/2017 and FSA Regulation no. 5/2018
- Notification shares buy-back: DIGI COMMUNICATIONS N.V. reports to the regulated market the transactions which occurred under the DIGI symbol, 2 – 6 Mar 2020
- « La levée du pilon sur la plate-forme » peut faire la différence entre le saint et l’ordinaire
- Notification shares buy-back: DIGI COMMUNICATIONS N.V. reports to the regulated market the transactions which occurred under the DIGI symbol, 24 – 28 Feb 2020
- EH GROUP ENGINEERING awarded EU Horizon 2020
- Notification shares buy-back: DIGI COMMUNICATIONS N.V. reports to the regulated market the transactions which occurred under the DIGI symbol, 17 – 21 Feb 2020
- Digi Communications NV announces the release of the Preliminary Financial Results for year ended 31 December 2019
- Notification shares buy-back: DIGI COMMUNICATIONS N.V. reports to the regulated market the transactions which occurred under the DIGI symbol, 10 – 14 Feb 2020
- Reporting of legal documents concluded by DIGI Communications N.V. in January 2020 or in other period but effective in January 2020, in accordance with article 82 of Law no. 24/2017 and FSA Regulation no. 5/2018
- Digi Communications NV announces Investor Call on the Preliminary Financial Results for the year ended 31 December 2019
- Consolidation Looms for Fast-Growing Customer Data Platform Industry: CDP Institute Report
- Notification shares buy-back: DIGI COMMUNICATIONS N.V. reports to the regulated market the transactions which occurred under the DIGI symbol, 3–7 Feb 2020
- Digi Communications N.V. hereby reports successful closing of the offering of senior secured notes by RCS & RDS S.A., its Romanian subsidiary
- Notification shares buy-back: DIGI COMMUNICATIONS N.V. reports to the regulated market the transactions which occurred under the DIGI symbol, 27 – 31 Jan 2020
- Digi Communications N.V.: Independent Limited Assurance Report issued by the external auditor on 30 Jan 2020 regarding the information included in the current reports under Law 24/2017 (Article 82) and FSA Regulation no. 5/2018
- Digi Communications N.V.: Rectification of the report published on 15 Jan 2020, regarding legal documents concluded by DIGI COMMUNICATIONS N.V. in other periods but effective in Dec 2019, in accordance with article 82 of Law no. 24/2017 and FSA Regulation no. 5/2018
- Digi Communications N.V. reports the upsize and successful pricing of the offering of senior secured notes by RCS & RDS S.A., its Romanian subsidiary
- RCH To Present New Smart ECR, Robust and Vintage POS Systems at EuroShop 2020
- Notification shares buy-back: DIGI COMMUNICATIONS N.V. reports to the regulated market the transactions which occurred under the DIGI symbol, 20 – 24 Jan 2020
- Digi Communications N.V.: (i) launch of an offering by RCS & RDS S.A. of senior secured notes; (ii) issuance of a notice of conditional full redemption of all outstanding €550.0m 5.0% senior secured notes due 2023 issued by the Company and (iii) restatement by the Company of its unaudited interim condensed consolidated financial statements for the 9-month period ended 30 Sep 2019
- Notification shares buy-back: DIGI COMMUNICATIONS N.V. reports to the regulated market the transactions which occurred under the DIGI symbol, 13 – 17 Jan 2020
- Reporting of legal documents concluded by DIGI Communications N.V. in December 2019 or in other period but effective in December 2019, in accordance with article 82 of Law no. 24/2017 and FSA Regulation no. 5/2018
- Notification shares buy-back: DIGI COMMUNICATIONS N.V. reports to the regulated market the transactions which occurred under the DIGI symbol, 6 – 10 Jan 2020
- Berlin-based SuitePad named Best Places to Work in Hotel Tech 2020 category at HotelTechReport.com’s HotelTechAwards
- Notification shares buy-back: DIGI COMMUNICATIONS N.V. reports to the regulated market the transactions which occurred under the DIGI symbol, 30 Dec 2019 – 3 Jan 2020
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