Secondary progressive multiple sclerosis
diseaseOn this page
Also known as secondary-progressive MSSPMS
Summary
Secondary progressive multiple sclerosis (MONDO:0000450) is a disease and 70 clinical trials. Top therapeutic interventions include siponimod, fexofenadine, and natalizumab. A subtype of chronic progressive multiple sclerosis — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Clinical trials: 70
Clinical features
No curated clinical features (Orphanet) for this disease.
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | secondary progressive multiple sclerosis |
| Mondo ID | MONDO:0000450 |
| EFO | EFO:0008522 |
| DOID | DOID:0050783 |
| ICD-11 | 1045965709 |
| SNOMED CT | 425500002 |
| UMLS | C0751965 |
| MedGen | 155969 |
| Is cancer (heuristic) | no |
Also known as: secondary-progressive MS · SPMS
Disease family
This is a subtype of chronic progressive multiple sclerosis. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.
Classification path: disease › human disease › disease by body system or component › nervous system disorder › central nervous system disorder › autoimmune disorder of central nervous system › multiple sclerosis › chronic progressive multiple sclerosis › secondary progressive multiple sclerosis
Related subtypes (2): primary progressive multiple sclerosis, progressive relapsing multiple sclerosis
Genetics & variants
GWAS landscape
No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.
Variant details and genetic-evidence tiers
No tiered GWAS variants or ClinVar records for this disease.
Genes & proteins
No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).
Function
No pathway enrichment — requires an associated-gene cohort.
Therapeutics
Drugs indicated for this disease
1 approved, 8 in late-stage (phase 3) trials. Disease-direct ChEMBL indications, not inferred from the associated-gene cohort below.
| Drug | Development status |
|---|---|
| Ocrelizumab | Approved (phase 4) |
| Dalfampridine | Phase 3 (in late-stage trials) |
| Dirucotide | Phase 3 (in late-stage trials) |
| Mitoxantrone | Phase 3 (in late-stage trials) |
| Natalizumab | Phase 3 (in late-stage trials) |
| Simvastatin | Phase 3 (in late-stage trials) |
| Siponimod | Phase 3 (in late-stage trials) |
| Teriflunomide | Phase 3 (in late-stage trials) |
| Tolebrutinib | Phase 3 (in late-stage trials) |
Earlier-phase candidates (phase 2, investigational — efficacy not yet established): Amiloride, Corticotropin, Estriol, Fluoxetine, Glatiramer Acetate, Lamotrigine, Lipoic Acid, Alpha, Norethindrone, Riluzole, Rituximab, Sodium Chloride.
Clinical trials & evidence
Clinical trials
Clinical trials: 70.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 23 |
| PHASE2 | 14 |
| PHASE3 | 10 |
| PHASE1 | 9 |
| PHASE1/PHASE2 | 6 |
| PHASE2/PHASE3 | 4 |
| PHASE4 | 2 |
| EARLY_PHASE1 | 2 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT02208050 | PHASE4 | COMPLETED | A Study of the Effectiveness of Fampridine in Improving Upper Limb Function in MS |
| NCT04792567 | PHASE4 | COMPLETED | Exploring the Immune Response to SARS-CoV-2 modRNA Vaccines in Patients With Secondary Progressive Multiple Sclerosis (AMA-VACC) |
| NCT04047628 | PHASE3 | RECRUITING | Best Available Therapy Versus Autologous Hematopoietic Stem Cell Transplant for Multiple Sclerosis (BEAT-MS) |
| NCT04688788 | PHASE3 | ACTIVE_NOT_RECRUITING | Non-inferiority Study of Ocrelizumab and Rituximab in Active Multiple Sclerosis |
| NCT06372145 | PHASE3 | ACTIVE_NOT_RECRUITING | A Study to Investigate Long-term Safety and Tolerability of Tolebrutinib in Participants With Multiple Sclerosis. |
| NCT07225504 | PHASE3 | RECRUITING | A Study to Evaluate the Efficacy and Safety of Remibrutinib in Secondary Progressive Multiple Sclerosis |
| NCT07299019 | PHASE3 | RECRUITING | A Study of Orelabrutinib in Patients With Secondary Progressive Multiple Sclerosis |
| NCT00146159 | PHASE3 | TERMINATED | Study Evaluating Mitoxantrone in Multiple Sclerosis |
| NCT00869726 | PHASE2/PHASE3 | COMPLETED | A Study for Patients With Secondary Progressive Multiple Sclerosis |
| NCT00870155 | PHASE2/PHASE3 | TERMINATED | A Study for Patients With Multiple Sclerosis |
| NCT01416181 | PHASE3 | TERMINATED | A Clinical Study of the Efficacy of Natalizumab on Reducing Disability Progression in Participants With Secondary Progressive Multiple Sclerosis |
| NCT01665144 | PHASE3 | COMPLETED | Exploring the Efficacy and Safety of Siponimod in Patients With Secondary Progressive Multiple Sclerosis (EXPAND) |
| NCT01917019 | PHASE3 | COMPLETED | A Safety and Efficacy Study of Oral Prolonged-Release Fampridine (BIIB041) in Japanese Participants With Multiple Sclerosis |
| NCT03315923 | PHASE2/PHASE3 | COMPLETED | Comparison of Clinical Effects of Rituximab and Glatiramer Acetate in Secondary Progressive Multiple Sclerosis Patients |
| NCT03387670 | PHASE3 | COMPLETED | Multiple Sclerosis-Simvastatin Trial 2 |
| NCT04925557 | PHASE2/PHASE3 | TERMINATED | Study to Assess the Efficacy of Mayzent on Microglia in Secondary Progressive Multiple Sclerosis |
| NCT05893225 | PHASE2 | ACTIVE_NOT_RECRUITING | Metformin Add-on Clinical Study in Multiple Sclerosis to Evaluate Brain Remyelination And Neurodegeneration |
| NCT06292923 | PHASE2 | RECRUITING | A Study of Nasal Foralumab in Non-Active Secondary Progressive Multiple Sclerosis Patients |
| NCT06599307 | PHASE2 | RECRUITING | The Effect of Rituximab on Cognitive and Hand Functions in Secondary Progressive Multiple Sclerosis |
| NCT06961383 | PHASE2 | NOT_YET_RECRUITING | Study of NG01 Cell Therapy in Secondary Progressive Multiple Sclerosis |
| NCT07477639 | PHASE1/PHASE2 | RECRUITING | Treatment of Participants With Primary or Secondary Progressive Multiple Sclerosis |
| NCT00257855 | PHASE2 | COMPLETED | A Randomised Controlled Trial of Neuroprotection With Lamotrigine in Secondary Progressive Multiple Sclerosis |
| NCT00647348 | PHASE2 | COMPLETED | Investigation of Simvastatin in Secondary Progressive Multiple Sclerosis |
| NCT01077466 | PHASE2 | COMPLETED | Natalizumab Treatment of Progressive Multiple Sclerosis |
| NCT01181089 | PHASE1/PHASE2 | WITHDRAWN | Dose Escalation Study to Evaluate the Penetration and Pharmacodynamic Effects of Baminercept in the Cerebrospinal Fluid (CSF)and Safety in Subjects With Secondary Progressive Multiple Sclerosis (SPMS) |
| NCT01191996 | PHASE1/PHASE2 | COMPLETED | Safety Study of an Immunomodulating Microparticle to Treat Progressive Multiple Sclerosis |
| NCT01228396 | PHASE2 | UNKNOWN | AIMSPRO in the Treatment of Bladder Dysfunction in Secondary Progressive Multiple Sclerosis |
| NCT01466114 | PHASE2 | UNKNOWN | Estriol Treatment in Multiple Sclerosis (MS): Effect on Cognition |
| NCT01684761 | PHASE2 | COMPLETED | Study of Tcelna (Imilecleucel-T) in Secondary Progressive Multiple Sclerosis |
| NCT01910259 | PHASE2 | COMPLETED | MS-SMART: Multiple Sclerosis-Secondary Progressive Multi-Arm Randomisation Trial |
| NCT01950234 | PHASE2 | TERMINATED | ACTH in Progressive Forms of MS |
| NCT02228213 | PHASE2 | COMPLETED | Safety and Efficacy Study of MIS416 to Treat Secondary Progressive Multiple Sclerosis |
| NCT02495766 | PHASE1/PHASE2 | COMPLETED | Autologous Mesenchymal Stromal Cells for Multiple Sclerosis |
| NCT03283826 | PHASE1/PHASE2 | TERMINATED | Phase 1/2 Study to Evaluate the Safety and Efficacy of ATA188 in Subjects With Progressive Multiple Sclerosis |
| NCT03696485 | PHASE1/PHASE2 | WITHDRAWN | Study to Assess the Safety and Efficacy of an IT Administration of SCM-010 in SPMS |
| NCT03896217 | PHASE2 | COMPLETED | Simvastatin in Secondary Progressive Multiple Sclerosis |
| NCT03783416 | PHASE1 | RECRUITING | SIZOMUS Safety of Ixazomib Targeting Plasma Cells in Multiple Sclerosis |
| NCT00559702 | PHASE1 | COMPLETED | Safety Study of Natalizumab to Treat Multiple Sclerosis (MS) |
| NCT00813969 | PHASE1 | COMPLETED | Autologous Mesenchymal Stem Cell (MSC) Transplantation in MS |
| NCT02253264 | PHASE1 | COMPLETED | A Phase 1 Trial of Intrathecal Rituximab for Progressive Multiple Sclerosis Patients |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| SIPONIMOD | 4 | 6 |
| FEXOFENADINE | 4 | 3 |
| NATALIZUMAB | 4 | 3 |
| OCRELIZUMAB | 4 | 3 |
| AMILORIDE | 4 | 1 |
| CORTICOTROPIN | 4 | 1 |
| DALFAMPRIDINE | 4 | 1 |
| ELASOMERAN | 4 | 1 |
| ESTRIOL | 4 | 1 |
| FERUMOXYTOL | 4 | 1 |
| GADOTERIDOL | 4 | 1 |
| GLATIRAMER ACETATE | 4 | 1 |
| LAMOTRIGINE | 4 | 1 |
| MITOXANTRONE | 4 | 1 |
| NORETHINDRONE | 4 | 1 |
| RILUZOLE | 4 | 1 |
| TERIFLUNOMIDE | 4 | 1 |
| DIRUCOTIDE | 3 | 2 |
| LIPOIC ACID, ALPHA | 3 | 1 |
| ORELABRUTINIB | 3 | 1 |
| REMIBRUTINIB | 3 | 1 |
| TOLEBRUTINIB | 3 | 1 |
| TRICAPRILIN | 3 | 1 |
| BAMINERCEPT | 2 | 1 |
| EVRULEUCEL | 2 | 1 |
| CHEMBL4082273 | 0 | 1 |
| CHEMBL4579631 | 0 | 1 |
| CHEMBL4776881 | 0 | 1 |
| IMILECLEUCEL-T | -1 | 1 |
Related Atlas pages
- Drugs: Siponimod, Fexofenadine, Natalizumab, Ocrelizumab, Amiloride, Corticotropin, Dalfampridine, Elasomeran, Estriol, Ferumoxytol, Gadoteridol, Glatiramer Acetate, Lamotrigine, Mitoxantrone, Norethindrone, Riluzole, Teriflunomide, Dirucotide, Lipoic Acid, Alpha, Orelabrutinib, Remibrutinib, Tolebrutinib, Tricaprilin