1. New treatment possibilities for rheumatoid arthritis: the Russian experience in using certolizumab pegol
- Author
-
Dmitry Evgenyevich Karateev, E L Nasonov, L N Denisov, M L Stanislav, E Yu Panasyuk, I A Andrianova, V I Mazurov, E S Zhugrova, Yu P Uspensky, L N Belousova, E P Ilivanova, G K Matsiyevskaya, G P Aurtyunov, K A Lytkina, R S Saikovsky, V N Ardashev, E V Zhilyaev, and N I Korshunov
- Subjects
Drug ,rheumatoid arthritis ,medicine.medical_specialty ,media_common.quotation_subject ,Immunology ,Diseases of the musculoskeletal system ,Gastroenterology ,law.invention ,Rheumatology ,Randomized controlled trial ,law ,Internal medicine ,medicine ,Immunology and Allergy ,Certolizumab pegol ,rapid 1 ,media_common ,rapid 2 ,business.industry ,Incidence (epidemiology) ,medicine.disease ,randomized clinical trial ,Clinical trial ,certolizumab pegol ,RC925-935 ,Rheumatoid arthritis ,Methotrexate ,Tumor necrosis factor alpha ,business ,medicine.drug - Abstract
Certolizumab pegol (CZP) is a new drug from the group of tumor necrosis factor a inhibitors. The efficacy and safety CZP in the treatment of rheumatoid arthritis (RA) have been studied in the international 52-week RAPID-1 and 24-week RAPID-2 clinical trials that studied the use of CZP in combination with methotrexate (MTX) in patients with active RA unresponsive to MTX. The study populations of the RAPID 1 and RAPID 2 trials constituted the major portion of Russian patients (11.8 and 18.4%, respectively), including that in the prolonged open-labeled phases. The results of using CZP in Russian patients in the RAPID trials showed that they displayed a highly stable response to treatment and a rapidly developing clinical effect, that a therapy response could be predicted in the first 12 weeks, and that the incidence of local postinjection reactions was low.
- Published
- 2012