StarMS
What it found
A paper reports the results; we have not read it yet. See Papers below.
What was tested
Treatment tested
- Cyclophosphamide anhydrous
- Filgrastim
Granulocyte colony stimulating factor receptor agonist
- Rabbit anti-human thymocyte immunoglobulin
- Lenograstim
Granulocyte colony stimulating factor receptor agonist
Compared with
- Alemtuzumab
CAMPATH-1 antigen inhibitor
- Ocrelizumab
B-lymphocyte antigen CD20 binding agent
What it measured
Main measures
Proportion of patients who have maintained NEDA status (defined as the absence of all three of the following: protocol defined clinical relapses; 6 months confirmed EDSS progression of at least 1 point with an absence of relapse at the time of assessment; any evidence of MRI disease activity as defined by T1 Gd-enhanced lesion or new and/or enlarging T2 lesion after month 6) in the 2-year post-ran
Disability progressionRelapsesMRI lesions
Other measures (2)
Safety
SafetyCurrent key secondary outcomes as of 06/05/2026: Safety assessed using: 1. Serious adverse event (SAE) rate within the 2-year follow up period 2. Mortality rate (grade 5 SAEs) within the 2-year follow up period 3. Combined grade 4 and 5 SAE rates within the 2-year follow up period 4. Total number of adverse events (AEs) experienced in the 100 days post-randomisation 5. Total number of AEs within t
Disability progressionRelapsesMRI lesionsRetina scans (OCT)VisionThinking and memoryFatiguePainMood and sleepQuality of life (reported by participants)Immune responseSafety
Who could take part
Relapsing MS · 16 to 55
Inclusion: 1. Diagnosis of MS using the 2017 McDonald criteria. Exclusion: 1. Diagnosis of primary or secondary progressive MS.
As registered. Criteria can change, so ask the trial team or your neurologist.
About this trial
In the sponsor's words
The main objective of this trial is to assess whether autologous haematopoietic stem cell transplantation (aHSCT) is more effective at maintaining clinical stability in patients with highly active relapsing remitting multiple sclerosis (RRMS) than treatment with a disease modifying therapy (alemtuzumab or ocrelizumab).
Papers
Loading reviews and guidelines…
Related trials
History
Started
Feb 2020
Finished
Sept 2026
Assembled by software from public sources and not checked by people. Each record links to its source. Report an error