O'HAND
What it found
The main measure showed a statistically significant benefit.
| Measure | Estimate | 95% CI | p |
|---|---|---|---|
| Time to Onset of cCDP12 in Magnetic Resonance Imaging (MRI) Activity Analysis Set | Hazard Ratio (HR) 0.45 | 0.31–0.64 | <.0001 |
| Time to Onset of 12-week Composite Confirmed Disability Progression (cCDP12) in FAS | Hazard Ratio (HR) 0.70 | 0.57–0.86 | 0.0007 |
Statistical analysis as posted on ClinicalTrials.gov.
What was tested
Treatment tested
- Ocrelizumab
B-lymphocyte antigen CD20 binding agent
Placebo or sham
- Placebo
- Placebo Ocrevus
Results by group
Time to Onset of 12-week Composite Confirmed Disability Progression (cCDP12) in FAS
Up to approximately 243 weeks
| Group | Value | Interval | Number analysed |
|---|---|---|---|
| Ocrelizumab | 204.9 weeks | 504 | |
| Placebo | 133.6 weeks | 121.9–168.1 | 507 |
Ocrelizumab
Placebo
p = 0.0007; Hazard Ratio (HR) 0.70 (95% CI 0.57–0.86)
Time to Onset of cCDP12 in Magnetic Resonance Imaging (MRI) Activity Analysis Set
Up to approximately 243 weeks
| Group | Value | Interval | Number analysed |
|---|---|---|---|
| Ocrelizumab | Not reached | 183 | |
| Placebo | 124.9 weeks | 185 |
p = <.0001; Hazard Ratio (HR) 0.45 (95% CI 0.31–0.64)
Values as posted on ClinicalTrials.gov. Outcomes measured differently across trials are not directly comparable.
Safety
| Group | Participants at risk | Serious adverse events | Deaths |
|---|---|---|---|
| Ocrelizumab | 506 | 65 (12.8%) | 16 |
| Placebo | 506 | 68 (13.4%) | 14 |
As posted on ClinicalTrials.gov. Serious adverse events include any serious health event during the trial, whether or not the treatment caused it.
What it measured
Main measures
Time to Onset of 12-week Composite Confirmed Disability Progression (cCDP12) in FAS
Up to approximately 243 weeks
Disability progressionArm and hand functionTime to Onset of cCDP12 in Magnetic Resonance Imaging (MRI) Activity Analysis Set
Up to approximately 243 weeks
Disability progressionMRI lesionsArm and hand functionUpper limb disability progression, measured based on time to 20% worsening from baseline in 9-HPT confirmed for at least 12 weeks and in all patients and patients with MRI activity.
Disability progressionMRI lesionsArm and hand function1. Time to onset of composite 12-week CDP defined as the time from randomization to the first occurrence of either 12-week CDP in 9-HPT, or 12-week CDP in EDSS
Disability progression
Other measures (21)
Time to 12-week CDP in 9-HPT
Up to approximately 243 weeks
Disability progressionArm and hand functionTime to 12-week CDP in EDSS
Up to approximately 243 weeks
Disability progressionFatigueBladder, bowel and sexual functionTime to 24-week CDP in 9-HPT
Up to approximately 243 weeks
Disability progressionArm and hand functionTime to 24-week CDP in EDSS
Up to approximately 243 weeks
Disability progressionFatigueBladder, bowel and sexual functionAnnual Rate of Change From Baseline in Radius of Total Volume of T2 Lesions
Up to approximately 120 weeks
MRI lesionsAnnual Rate of Percent Change From Week 24 in Total Brain Volume
From Week 24 up to approximately 120 weeks
MRI lesionsBrain volume lossNumber of Participants With Adverse Events (AEs) and Serious Adverse Events (SAEs)
From initiation of study drug up to approximately 10.5 years
SafetySerum Concentration of Ocrelizumab
Up to approximately 10.5 years
How the body handles the medicineB-cell Levels in Blood
Baseline, Weeks 2, 12, 24, 36, 48, 60, 72, 84, 96, 108, 120, 132, 144, 156, 168, 180, 192, 204 and 228
Immune responseChange From Baseline in B-cell Levels
Weeks 2, 12, 24, 36, 48, 60, 72, 84, 96, 108, 120, 132, 144, 156, 168, 180, 192, 204 and 228
Immune response
Who could take part
Progressive MS · 18 to 65
Inclusion Criteria: * EDSS score at screening and baseline >= 3.0 to 8.0, inclusive * Disease duration from the onset of MS symptoms relative to randomization date: Less than 20 years in participants with an EDSS score at screening 7.0 - 8.0 Less than 15 years in participants with an EDSS at screening 5.5 - 6.5 Less than 10 years in participants with an EDSS at screening \<= 5.0 * Documented history or presence at screening of at least one of the following laboratory findings in a cerebrospinal fluid specimen: Elevated immunoglobulin G (IgG) index or one or more IgG oligoclonal bands detected by isoelectric focusing * Screening and baseline 9-HPT completed in > 25 seconds (average of the two hands) * Neurological stability for ≥ 30 days prior to baseline * Ability to complete the 9-HPT within 240 seconds with each hand at screening and baseline * Neurological stability for >/= 30 days prior to baseline * Participants previously treated with immunosuppressants, immunomodulators, or other immunomodulatory therapies must undergo an appropriate washout period according to the local label of the immunosuppressant/immunomodulatory drug used * For women of childbearing potential: agreement to remain abstinent (refrain from heterosexual intercourse) or use adequate contraceptive methods during the treatment period and for 6 or 12 months after the final dose of ocrelizumab. Adherence to local requirements, if more stringent, is required. * For female participants without reproductive potential: Women may be enrolled if surgically sterile (i.e hysterectomy, complete bilateral oophorectomy) or post-menopausal unless the participant is receiving a hormonal therapy for her menopause or if surgically sterile Exclusion Criteria: * History of relapsing-remitting or secondary progressive MS at screening * Confirmed serious opportunistic infection including: active bacterial, viral, fungal, mycobacterial infection or other infection, including tuberculosis or atypical mycobacterial disease * Participants who have or have had confirmed or a high degree of suspicion of progressive multifocal leukoencephalopathy (PML) * Known active malignancy or are being actively monitored for recurrence of malignancy * Immunocompromised state * Receipt of a live-attenuated vaccine within 6 weeks prior to randomization * Inability to complete an MRI or contraindication to Gd administration. * Participants requiring symptomatic treatment of MS and/or physiotherapy who are not on a stable regimen. Participants must not initiate symptomatic treatment of MS or physiotherapy within 4 weeks of randomization. * Contraindications to mandatory premedications for infusion-related reactions, including: uncontrolled psychosis for corticosteroids and closed-angle glaucoma for antihistamines * Known presence of other neurologic disorders * Pregnant or breastfeeding, or intending to become pregnant during the study and for 6 or 12 months after last infusion of the study drug * Lack of peripheral venous access * Significant, uncontrolled disease, such as cardiovascular, pulmonary, renal, hepatic, endocrine or gastrointestinal, or any other significant disease that may preclude participant from participating in the study * Any concomitant disease that may require chronic treatment with systemic corticosteroids or immunosuppressants during the course of the study * History of alcohol or other drug abuse * History of primary or secondary immunodeficiency * Treatment with any investigational agent within 24 weeks prior to screening (Visit 1) or 5 half-lives of the investigational drug (whichever is longer), or treatment with any experimental procedure for MS * Previous treatment with B-cell targeting therapies * Any previous treatment with bone marrow transplantation and hematopoietic stem cell transplantation * Any previous history of transplantation or anti-rejection therapy * Treatment with IV Ig or plasmapheresis within 12 weeks prior to randomization * Systemic corticosteroid therapy within 4 weeks prior to screening * Positive serum human chorionic gonadotropin (hCG) measured at screening or positive urine β-hCG at baseline * Positive screening tests for hepatitis B * Any additional exclusionary criterion as per ocrelizumab (Ocrevus®) local label, if more stringent than the above * Lack of MRI activity at screening/baseline if more than 650 participants without MRI activity have already been enrolled, as defined by T1 Gd+ lesion(s) and/or new and/or enlarged T2 lesion(s) in the screening, to ensure that at least 350 participants with MRI activity will be randomized Eligibility Criteria for OLE Phase: * Completed the 144 weeks of double-blind treatment phase of the trial or are ongoing in the double blind treatment phase at the time of the primary analysis, and who, in the opinion of the investigator, may benefit from treatment with Ocrelizumab. Participants who withdrew from study treatment and received another DMT or commercial ocrelizumab will not be allowed to enter in the OLE phase. * For women of childbearing potential: agreement to remain abstinent (refrain from heterosexual intercourse) or use adequate contraceptive methods during the treatment period and for 6 or 12 months after the final dose of ocrelizumab. Adherence to local requirements, if more stringent, is required. * For female participants without reproductive potential: Women may be enrolled if surgically sterile (i.e. hysterectomy, complete bilateral oophorectomy) or post-menopausal unless the participant is receiving a hormonal therapy for her menopause or if surgically sterile
As registered. Criteria can change, so ask the trial team or your neurologist.
About this trial
In the sponsor's words
This study will evaluate the efficacy and safety of ocrelizumab (Ocrevus®) compared with placebo in participants with primary progressive multiple sclerosis (PPMS), including participants later in their disease course. This study will consist of the following phases: screening, double-blind treatment, an optional post-double-progression ocrelizumab (PDP OCR) treatment, follow-up 1 (FU1), an optional open-label extension (OLE), and follow-up 2 (FU2).
Papers
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Extended by
OleroMAXPhase 3 · Recruiting
Links found where a registry record names another trial's registry number.
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History
Started
Aug 2019
Main results due
Jan 2025
Finished
Jan 2028
Results posted
Feb 2026
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