Overview
A Study of RoActemra/Actemra (Tocilizumab) Versus Placebo in Patients With Systemic Sclerosis
Status:
Completed
Completed
Trial end date:
2015-08-01
2015-08-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
This multicenter, randomized, double-blind, placebo-controlled, two-arm, parallel-group study will evaluate the efficacy and safety of RoActemra/Actemra (tocilizumab) in participants with systemic sclerosis. Participants will be randomized to receive either RoActemra/Actemra 162 mg subcutaneously weekly or placebo for 48 weeks. From Week 48 to Week 96, all participants will receive open-label RoActemra/Actemra 162 mg subcutaneously weekly. Anticipated time on study treatment is 96 weeks.Phase:
Phase 3Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Hoffmann-La Roche
Criteria
Inclusion Criteria:- Adult patients, >/= 18 years of age
- Systemic sclerosis, as defined by American College of Rheumatology (1980) criteria
- Disease duration of = 60 months (defined as time from first non-Raynaud phenomenon
manifestation)
- >/= 15 and = 40 mRSS units at screening
- Active disease, as defined by protocol
- Uninvolved skin at injection sites
- Negative pregnancy test for a female subject of childbearing potential
Exclusion Criteria:
- Major surgery (including joint surgery) within 8 weeks prior to and/or during study
enrollment
- Rheumatic autoimmune disease other than systemic sclerosis
- Skin thickening (scleroderma) limited to areas distal to the elbows or knees at
screening
- Previous treatment with tocilizumab
- History of severe allergic or anaphylactic reactions to human, humanized, or murine
monoclonal antibodies
- Severe cardiopulmonary disease
- Known active current or history of recurrent infections
- Use of any investigational, biologic, or immunosuppressive therapies including
intra-articular or parenteral corticosteroids prior to study enrollment as specified
in the protocol
- As specified in the protocol, any current or past medical condition or medical history
involving but not limited to the nervous, renal, pulmonary, endocrine, and
gastrointestinal organ systems determined by the Principal Investigator to pose a
significant safety risk to any subject while participating in the study
- Primary or secondary immunodeficiency