EUCTR2015-005597-38-ES
Active, not recruiting
Phase 1
An open-label study to evaluate the efficacy and safety of ocrelizumab in patients with relapsing remitting multiple sclerosis who have a suboptimal response to an adequate course of disease-modifying treatment - CASTING
Roche Farma S.A. que representa en España a F. Hoffmann-La Roche Ltd0 sites600 target enrollmentMarch 18, 2016
ConditionsRelapsing remitting multiple sclerosis (RRMS)MedDRA version: 18.1Level: PTClassification code 10028245Term: Multiple sclerosisSystem Organ Class: 10029205 - Nervous system disordersMedDRA version: 18.1Level: PTClassification code 10063399Term: Relapsing-remitting multiple sclerosisSystem Organ Class: 10029205 - Nervous system disordersMedDRA version: 18.1Level: PTClassification code 10048393Term: Multiple sclerosis relapseSystem Organ Class: 10029205 - Nervous system disordersMedDRA version: 18.1Level: LLTClassification code 10039720Term: Sclerosis multipleSystem Organ Class: 10029205 - Nervous system disordersTherapeutic area: Diseases [C] - Nervous System Diseases [C10]
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- Relapsing remitting multiple sclerosis (RRMS)
- Sponsor
- Roche Farma S.A. que representa en España a F. Hoffmann-La Roche Ltd
- Enrollment
- 600
- Status
- Active, not recruiting
- Last Updated
- 9 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •\- Age 18\-55 years
- •\- Have a definite diagnosis of RRMS, confirmed as per the revised McDonald 2010 criteria of \<\= 5 years
- •\- Have a length of disease duration, from first symptom, of \< 10 years
- •\- Have received no more than two prior disease modifying treatments (DMTs), and the discontinuation of the most recent DMT was due to lack of efficacy
- •\- Suboptimal disease control while on a DMT
- •\- EDSS of 0\.0 to 4\.0, inclusive, at screening
- •\- For women of childbearing potential: agreement to use an acceptable birth control method during the treatment period and for at least 6 months after the last dose of study drug
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1\.2 Adults (18\-64 years) yes
Exclusion Criteria
- •\- Secondary progressive multiple sclerosis (SPMS) or history of primary progressive or progressive relapsing MS
- •\- Inability to complete an MRI
- •\- Known presence of other neurological disorders
- •Exclusions Related to General Health
- •\- Any concomitant disease that may require chronic treatment with systemic corticosteroids or immunosuppressants during the course of the study
- •\- History or currently active primary or secondary immunodeficiency
- •\- History of severe allergic or anaphylactic reactions to humanized or murine monoclonal antibodies
- •\- History of opportunistic infections
- •\- History or known presence of recurrent or chronic infection
- •\- History of malignancy
Outcomes
Primary Outcomes
Not specified
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