Being tested
S1P receptor modulation (lymphocyte trafficking): reduce relapses and new lesions in relapsing MS
Trial timeline
Trial start year. Dot size reflects participants where reported. Only trials that count towards the status are shown.
relapsing MS · S1P receptor modulation (lymphocyte trafficking)
Trials are running now and no controlled trial has a readable result yet.
- Trials
- 33
- Running now
- 5
- Controlled phase 2/3 trials
- 16
- People in controlled trials
- 10683
Deciding trials (phase 3): 7 met, 0 did not.
Other linked trials: 26
Dose comparisons, trials against another medicine, add-on trials, phase 1 and uncontrolled studies. They are listed below but do not set the status.
Trials
Phase 3 · 2014 · Compared with interferon beta-1a · MSFT-NCT02294058
Phase 3 · 2014 · Placebo-controlled · MSFT-NCT01941004
Phase 3 · 2013 · Compared with interferon beta-1a · MSFT-NCT02047734
Phase 3 · 2013 · Compared with interferon beta-1a · MSFT-NCT01892722
Phase 3 · 2012 · Compared with glatiramer acetate · MSFT-NCT01633112
Treatment with fingolimod, 0.5 mg, was superior to treatment with glatiramer acetate, 20 mg, in reducing ARR (40.7% relative reduction); the relative reduction with fingolimod, 0.25 mg, was 14.6%, which was not statistically significant (for fingolimod, 0.5 mg, ARR, 0.15; 95% CI, 0.11-0.21; for fingolimod, 0.25 mg, ARR, 0.22; 95% CI, 0.17-0.29; for glatiramer acetate, 20 mg, ARR, 0.26; 95% CI, 0.20-0.34).
Read by software from the paper's abstractPhase 3 · 2011 · Placebo-controlled · MSFT-NCT01499667
Phase 3 · 2008 · Placebo-controlled · MSFT-2008-002096-27
Phase 3 · 2006 · Placebo-controlled · MSFT-NCT00355134
Mean annualised relapse rate was 0·40 (95% CI 0·34-0·48) in patients given placebo and 0·21 (0·17-0·25) in patients given fingolimod 0·5 mg: rate ratio 0·52 (95% CI 0·40-0·66; p<0·0001), corresponding to a reduction of 48% with fingolimod 0·5 mg versus placebo.
Read by software from the paper's abstractPhase 3 · 2006 · Placebo-controlled · MSFT-NCT00289978
The annualized relapse rate was 0.18 with 0.5 mg of fingolimod, 0.16 with 1.25 mg of fingolimod, and 0.40 with placebo (P<0.001 for either dose vs. placebo).
Read by software from the paper's abstractPhase 3 · 2005 · Placebo-controlled · MSFT-2005-000365-19
Other linked trials: 26
These linked trials do not set the status.
- COASTOngoing
Phase 4 · 2024 · Not randomised
Phase 4 · 2024 · Not randomised
- Study of Efficacy and Safety of Fingolimod (Gilenya) 0.5 mg in Chinese Patients With Relapsing Multiple Sclerosis (RMS) PatientsNo result found
Phase 4 · 2021 · Not randomised
- ENGYNEStopped, other reason
Phase 4 · 2013 · Not randomised
- EARLiMSMissed main goal
Phase 4 · 2011 · Not randomised
- IM047-050Ongoing
Phase 3 · 2025 · Compared with fingolimod
- PIONEEROngoing
Phase 3 · 2022 · Compared with fingolimod
- NEOSOngoing
Phase 3 · 2021 · Compared with fingolimod
- Efficacy and safety of ONO-4641 versus Interferon-β-1a in patients with multiple sclerosisStopped, other reason
Phase 3 · 2014 · Compared with interferon beta-1a
- Efficacy and safety of ONO-4641 versus Interferon-β-1a in patients with multiple sclerosisStopped, other reason
Phase 3 · 2014 · Compared with interferon beta-1a
The deciding phase and counts come from the Trial Bank’s fixed rules.
Lab evidence
Lab studies in animals or cells. Results in animals often do not hold in people, and these studies never change the status of an idea.
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History
- 2026-10-29Trials: 31 → 33
- 2026-10-28Trials: 33 → 31
- 2026-10-27First listed as Being tested
Related hypotheses
- S1P receptor modulation (lymphocyte trafficking): reduce relapses and new lesions in primary progressive MS
- S1P receptor modulation (lymphocyte trafficking): reduce relapses and new lesions in relapsing and progressive MS
- S1P receptor modulation (lymphocyte trafficking): reduce relapses and new lesions in secondary progressive MS
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