A randomized, double-blind, parallel-group, phase III study of shortening the dosing interval of subcutaneous tocilizumab monotherapy in patients with rheumatoid arthritis and an inadequate response to subcutaneous tocilizumab every other week: Results of the 12-week double-blind period. Issue 1 (2nd January 2018)
- Record Type:
- Journal Article
- Title:
- A randomized, double-blind, parallel-group, phase III study of shortening the dosing interval of subcutaneous tocilizumab monotherapy in patients with rheumatoid arthritis and an inadequate response to subcutaneous tocilizumab every other week: Results of the 12-week double-blind period. Issue 1 (2nd January 2018)
- Main Title:
- A randomized, double-blind, parallel-group, phase III study of shortening the dosing interval of subcutaneous tocilizumab monotherapy in patients with rheumatoid arthritis and an inadequate response to subcutaneous tocilizumab every other week: Results of the 12-week double-blind period
- Authors:
- Ogata, Atsushi
Tanaka, Yoshiya
Ishii, Tomonori
Kaneko, Motohide
Miwa, Hiroko
Ohsawa, Shino - Abstract:
- Abstract: Objective: To determine the efficacy and safety of subcutaneous tocilizumab (TCZ-SC) monotherapy every week (qw) versus every other week (q2w) in patients with rheumatoid arthritis who had an inadequate response to TCZ-SC q2w. Methods: Adult patients in Japan with inadequate response to TCZ-SC q2w were randomized to either TCZ-SC 162 mg qw monotherapy or TCZ-SC 162 mg q2w monotherapy for 12 weeks (double-blind). The primary endpoint was the change from baseline in adjusted Disease Activity Score 28-erythrocyte sedimentation rate (DAS28-ESR) at week 12. Efficacy, safety and pharmacokinetics were assessed. Results: TCZ-SC qw was superior to TCZ-SC q2w for adjusted mean change in DAS28-ESR from baseline to week 12. The difference in the change in DAS28-ESR between TCZ-SC qw and q2w was −1.21 (95%CI: −2.13, −0.30, p = .0108). A higher proportion of patients receiving TCZ-SC qw achieved DAS28-ESR remission/low disease activity than TCZ-SC q2w. Adverse events were 71.4% and 66.7% for TCZ-SC qw and q2w, respectively; infection was the most common event with one fatal case with TCZ-SC qw. Conclusions: In patients with inadequate response to TCZ-SC q2w, shortening the dosing interval to qw improved efficacy with acceptable tolerability. Occurrence of infection for both TCZ q2w and qw is important and needs careful attention.
- Is Part Of:
- Modern rheumatology. Volume 28:Issue 1(2018)
- Journal:
- Modern rheumatology
- Issue:
- Volume 28:Issue 1(2018)
- Issue Display:
- Volume 28, Issue 1 (2018)
- Year:
- 2018
- Volume:
- 28
- Issue:
- 1
- Issue Sort Value:
- 2018-0028-0001-0000
- Page Start:
- 76
- Page End:
- 84
- Publication Date:
- 2018-01-02
- Subjects:
- Dose interval -- rheumatoid arthritis -- subcutaneous -- tocilizumab
Rheumatology -- Periodicals
616.723005 - Journal URLs:
- http://firstsearch.oclc.org ↗
https://academic.oup.com/mr ↗
https://www.tandfonline.com/journals/imor20 ↗
http://informahealthcare.com/loi/mor ↗
http://link.springer-ny.com/link/service/journals/10165/index.htm ↗
http://link.springer.com/journal/10165 ↗
http://informahealthcare.com ↗ - DOI:
- 10.1080/14397595.2017.1332507 ↗
- Languages:
- English
- ISSNs:
- 1439-7595
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5895.300000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 5650.xml