Impact of Annual Versus Biannual Infusions of Ocrelizumab in Patients With Active MS,After 2 Years of Initial Treatment, on Freedom From Radiological Disease Activity at Two Years: a Multicenter Randomized Controlled Non-inferiority Trial: Autoimmune Diseases and Conditions – Multiple Sclerosis
2023 SEP 05 (NewsRx) -- By a
As a matter of record, on
Tracking Information
| Trial Identifier | NCT05999604 |
| First Submitted Date | |
| First Posted Date | |
| Results First Submitted Date | Not Provided |
| Results First Posted Date | Not Provided |
| Last Update Submitted Date | |
| Last Update Posted Date | |
| Primary Completion Date | |
| Start Date | |
| Current Primary Outcome Measures | •Absence of radiological disease activity at 2 years [ Time Frame: Months24 ] -- Percentage of patients with no new or enlarged T2 lesion >3mm on cerebrospinal MRI at 24 months compared with inclusion MRI. MRI readings at inclusion and M24 will be performed by an independent radiologist blinded to the treatment arm. |
| Current Secondary Outcome Measures | Not Provided |
| Other Outcome Measures | Not Provided |
| Change History | Complete list of historical revisions of study NCT05999604 |
Descriptive Information
| Brief Title | Impact of Annual Versus Biannual Infusions of Ocrelizumab in Patients With Active MS,After 2 Years of Initial Treatment, on Freedom From Radiological Disease Activity at Two Years: a Multicenter Randomized Controlled Non-inferiority Trial |
| Official Title | Impact of Annual Versus Biannual Infusions of Ocrelizumab in Patients With Active MS,After 2 Years of Initial Treatment, on Freedom From Radiological Disease Activity at Two Years: a Multicenter Randomized Controlled Non-inferiority Trial |
| Brief Summary | Multiple sclerosis (MS) is a chronic autoimmune disease of the central nervous system and the leading cause of severe non-traumatic disability in young people, affecting 110,000 people in |
| Detailed Description | Not Provided |
| Study Type | Interventional |
| Study Phase | Phase 3 |
| Study Design | Allocation: Randomized |
| Intervention Model: Parallel Assignment | |
| Primary Purpose: Treatment | |
| Masking: Single | |
| Condition | Multiple Sclerosis |
| Intervention | •Drug: Ocrelizumab Injection [Ocrevus] |
| spacinf of the injections from semestrial to annual administration | |
| Study Arms | •Experimental: annual ocrelizumab infusions |
| Interventions: | |
| ⚬Drug: Ocrelizumab Injection [Ocrevus] | |
| •Other: semestrial ocrelizumab infusions | |
| Interventions: | |
| ⚬Drug: Ocrelizumab Injection [Ocrevus] |
Recruitment Information
| Recruitment Status | Not yet recruiting |
| Estimated Enrollment | 244 |
| Estimated Completion Date | |
| Primary Completion Date | |
| Eligibility | Inclusion Criteria: Patient 18 years of age or older Presenting for a 4th semi-annual cycle of ocrelizumab (minimum) Requires follow-up MRI as part of treatment. Initial indication for ocrelizumab according to the marketing authorization (active MS, RR or SP form) Absence of relapse for at least 18 months (a relapse being defined as the appearance of new symptoms or worsening of existing symptoms, lasting more than 24 hours and outside a period of fever or an infectious episode; notified as a validated relapse by the neurologist in the patient’s file, treated or not with boluses of Solu-Medrol). EDSS between 0 and 6 inclusive Having received informed information about the study and having signed a consent to participate in the study French language proficiency Affiliated or beneficiary of a social insurance scheme Exclusion Criteria: Clinical forms of primary progressive MS Patients already receiving systematically spaced doses of ocrelizumab ≥ 9 months apart Contraindication to continued treatment with ocrelizumab (hypersensitivity reaction, ongoing active infection, development of malignancy since previous injection, development of severe immune deficiency) Planned pregnancy within 3 years Contraindication to MRI Contraindication to injection of contrast media Subject with severe or uncontrolled symptoms of renal, hepatic, hematological, gastrointestinal, pulmonary, psychiatric or cardiac disease, or any uncontrolled intercurrent pathology. Patient under legal protection Patients of childbearing age who do not wish to use effective contraception Pregnant or breast-feeding women |
| Sex/Gender | Sexes Eligible for Study: All |
| Ages | 18 years and older |
| No | |
| Contacts | Contact information is only displayed when the study is recruiting subjects |
| Listed Location Countries | Not Provided |
| Removed Location Countries |
Administrative Information
| NCT Number | NCT05999604 |
| Other Study ID Numbers | CBR_2022_13 |
| Has Data Monitoring Committee | Not Provided |
| Not Provided | |
| Plan to Share Data | No |
| Plan to Share Data (IPD) Description | Not Provided |
| Fondation Ophtalmologique Adolphe de Rothschild | |
| Collaborators | Not Provided |
| Investigators | Not Provided |
| Information Provided By | Fondation Ophtalmologique Adolphe de Rothschild |
| Verification Date |
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