Disease · EFO_0803536
multiple sclerosis symptom measurement
6 sourcesdiseases-2026-09-18-0.1.0
Cite this record
ConductScience Library. multiple sclerosis symptom measurement. Diseases, record EFO_0803536. Release diseases-2026-09-18-0.1.0, 18 Sept 2026. https://conductscience.org/library/diseases/EFO_0803536
On this page
Disease
Names and IDs as Open Targets gives them. Its IDs in MeSH, Orphanet, the Disease Ontology and the NCI Thesaurus are those Open Targets states for it.
- Name
- multiple sclerosis symptom measurement
- Open Targets ID
- EFO_0803536
- Other names
- Disseminated Sclerosis, MS, MS (Multiple Sclerosis), MULTIPLE SCLEROSIS ACUTE FULMINATING, Sclerosis, Disseminated, Sclerosis, Multiple, multiple sclerosis
- Highest stage of its drugs
- Approval, for 40 of its 279 drugs, from DailyMed, EMA Human Drugs, FDA, PMDA and TTD
Source Open Targets
Drugs279
The drugs Open Targets' clinical reports study for the disease, the highest stage first, then the most trial reports. The stage is Open Targets', the highest any of its sources reports for the pair, and each row names the sources that report it.
| Drug | ChEMBL ID | Type | Open Targets' stage | Stage reported by | Reports | Of them trials | Trials shown here | Source |
|---|---|---|---|---|---|---|---|---|
| INTERFERON BETA-1A | CHEMBL1201562 | Protein | Approval | DailyMed, EMA Human Drugs, PMDA and TTD | 95 | 84 | 83 | Drugs and targets |
| OCRELIZUMAB | CHEMBL2108041 | Antibody | Approval | DailyMed, EMA Human Drugs and TTD | 81 | 78 | 78 | Drugs and targets |
| FINGOLIMOD | CHEMBL314854 | Small molecule | Approval | EMA Human Drugs and TTD | 55 | 53 | 53 | Drugs and targets |
| NATALIZUMAB | CHEMBL1201607 | Antibody | Approval | DailyMed, EMA Human Drugs, FDA, PMDA and TTD | 59 | 52 | 52 | Drugs and targets |
| DIMETHYL FUMARATE | CHEMBL2107333 | Small molecule | Approval | DailyMed, EMA Human Drugs, PMDA and TTD | 61 | 51 | 51 | Drugs and targets |
| INTERFERON BETA-1B | CHEMBL1201563 | Protein | Approval | DailyMed, EMA Human Drugs and TTD | 56 | 50 | 49 | Drugs and targets |
| GLATIRAMER ACETATE | CHEMBL1201507 | Small molecule | Approval | DailyMed, PMDA and TTD | 53 | 49 | 49 | Drugs and targets |
| TERIFLUNOMIDE | CHEMBL973 | Small molecule | Approval | DailyMed, EMA Human Drugs and TTD | 42 | 39 | 39 | Drugs and targets |
| DALFAMPRIDINE | CHEMBL284348 | Small molecule | Approval | DailyMed, EMA Human Drugs and TTD | 36 | 31 | 30 | Drugs and targets |
| OFATUMUMAB | CHEMBL1201836 | Antibody | Approval | DailyMed and PMDA | 28 | 26 | 26 | Drugs and targets |
1 to 10 of 279
See all 279 drugsTargets352
The targets ChEMBL's mechanism records give for the disease's drugs, through Open Targets, the most drugs first. A mechanism record says what a drug acts on, not that the target causes the disease.
| Target | Protein | Its drugs that act on it | Mechanisms | Highest stage of those drugs | Gene in Genes | Source |
|---|---|---|---|---|---|---|
| NR3C1 | Glucocorticoid receptor | 17 | Glucocorticoid receptor agonist | Approval | https://conductscience.org/library/genes/2908 | Drugs and targets |
| S1PR1 | Sphingosine 1-phosphate receptor | 10 | Sphingosine 1-phosphate receptor Edg-1 agonist; Sphingosine 1-phosphate receptor Edg-1 modulator; Sphingosine 1-phosphate receptor agonist; Sphingosine 1-phosphate receptor binding agent; Sphingosine 1-phosphate receptor modulator | Approval | https://conductscience.org/library/genes/1901 | Drugs and targets |
| S1PR5 | Sphingosine 1-phosphate receptor | 6 | Sphingosine 1-phosphate receptor 5 modulator; Sphingosine 1-phosphate receptor agonist; Sphingosine 1-phosphate receptor binding agent; Sphingosine 1-phosphate receptor modulator | Approval | https://conductscience.org/library/genes/53637 | Drugs and targets |
| SCN10A | Sodium channel alpha subunit | 6 | Sodium channel alpha subunit blocker | Phase 2 | https://conductscience.org/library/genes/6336 | Drugs and targets |
| SCN11A | Sodium channel alpha subunit | 6 | Sodium channel alpha subunit blocker | Phase 2 | https://conductscience.org/library/genes/11280 | Drugs and targets |
| SCN1A | Sodium channel alpha subunit | 6 | Sodium channel alpha subunit blocker | Phase 2 | https://conductscience.org/library/genes/6323 | Drugs and targets |
| SCN2A | Sodium channel alpha subunit | 6 | Sodium channel alpha subunit blocker | Phase 2 | https://conductscience.org/library/genes/6326 | Drugs and targets |
| SCN3A | Sodium channel alpha subunit | 6 | Sodium channel alpha subunit blocker | Phase 2 | https://conductscience.org/library/genes/6328 | Drugs and targets |
| SCN4A | Sodium channel alpha subunit | 6 | Sodium channel alpha subunit blocker | Phase 2 | https://conductscience.org/library/genes/6329 | Drugs and targets |
| SCN5A | Sodium channel alpha subunit | 6 | Sodium channel alpha subunit blocker | Phase 2 | https://conductscience.org/library/genes/6331 | Drugs and targets |
1 to 10 of 352
See all 352 targetsTrials877
Trials an Open Targets clinical report links to the disease, posted results first, then the largest. A trial is shown when the release's checks confirm its link to the disease and Drugs and targets shows its link to one of the disease's drugs. 29 more are not shown, since the checks do not confirm them.
| Trial | Title | Phase | Participants | Results first posted | Conditions | Drugs | Linked by | Source |
|---|---|---|---|---|---|---|---|---|
| NCT01585298 | STudy to vAlidate telemetRic ECG Systems for firsT Dose Administration of Fingolimod (START) | Phase 4 | 6,998 | 2019-09-23 | Multiple Sclerosis | FINGOLIMOD | Its record names the disease | ClinicalTrials.gov |
| NCT01201356 | Long-term Safety and Tolerability of 0.5 mg Fingolimod in Patients With Relapsing Forms of Multiple Sclerosis | Phase 3 | 4,125 | 2019-11-07 | Relapsing Forms of Multiple Sclerosis | FINGOLIMOD | Its record names the disease | ClinicalTrials.gov |
| NCT03193866 | COMparison Between All immunoTherapies for Multiple Sclerosis. | 3,526 | 2025-04-20 | Relapsing-remitting Multiple Sclerosis | RITUXIMAB | Its record names the disease | ClinicalTrials.gov | |
| NCT02576717 | A Multi-Site, Open-Label Extension Trial of Oral RPC1063 in Relapsing Multiple Sclerosis | Phase 3 | 2,494 | 2024-01-30 | Multiple Sclerosis | OZANIMOD | Its record names the disease | ClinicalTrials.gov |
| NCT01707992 | The Efficacy, Safety, and Tolerability of Laquinimod in Participants With Relapsing Remitting Multiple Sclerosis (RRMS) | Phase 3 | 2,199 | 2019-03-13 | Multiple Sclerosis | LAQUINIMOD | Its record names the disease | ClinicalTrials.gov |
| NCT01064401 | Efficacy and Safety of BIIB019 (Daclizumab High Yield Process) Versus Interferon β 1a in Participants With Relapsing-Remitting Multiple Sclerosis | Phase 3 | 1,841 | 2016-07-11 | Relapsing-Remitting Multiple Sclerosis | DACLIZUMAB, INTERFERON BETA-1A | Its record names the disease | ClinicalTrials.gov |
| NCT00835770 | BG00012 Monotherapy Safety and Efficacy Extension Study in Multiple Sclerosis (MS) | Phase 3 | 1,736 | 2020-12-31 | Relapsing-Remitting Multiple Sclerosis | DIMETHYL FUMARATE | Its record names the disease | ClinicalTrials.gov |
| NCT01665144 | Exploring the Efficacy and Safety of Siponimod in Patients With Secondary Progressive Multiple Sclerosis (EXPAND) | Phase 3 | 1,651 | 2018-10-31 | Secondary Progressive Multiple Sclerosis | SIPONIMOD | Its record names the disease | ClinicalTrials.gov |
| NCT00906399 | Efficacy and Safety Study of Peginterferon Beta-1a in Participants With Relapsing Multiple Sclerosis | Phase 3 | 1,516 | 2014-09-19 | Relapsing Multiple Sclerosis | PEGINTERFERON BETA-1A | Its record names the disease | ClinicalTrials.gov |
| NCT01797965 | Long-Term Extension Study in Participants With Multiple Sclerosis Who Have Completed Study 205MS301 (NCT01064401) to Evaluate the Safety and Efficacy of BIIB019 | Phase 3 | 1,501 | 2019-12-04 | Relapsing-Remitting Multiple Sclerosis, Multiple Sclerosis | DACLIZUMAB | Its record names the disease | ClinicalTrials.gov |
1 to 10 of 877
See all 877 trialsComparisons in its trials277
Comparisons Trial comparisons calculated in the trials shown here, most participants first. A comparison in one of these trials does not always compare a treatment for the disease, so read the two groups.
| Comparison | Group 1, with the outcome | Group 2, with the outcome | Participants | Trial | Source |
|---|---|---|---|---|---|
| IFN Beta-1a 30 mcg vs DAC HYP 150 mg: serious adverse events | 194 of 922 | 221 of 919 | 1,841 | NCT01064401 | Trial comparisons |
| BG00012 240 mg BID vs BG00012 240 mg TID: Number of Participants With Treatment-Emergent Adverse Events (AEs) | 824 of 868 | 814 of 868 | 1,736 | NCT00835770 | Trial comparisons |
| BG00012 240 mg BID vs BG00012 240 mg TID: deaths from any cause | 5 of 868 | 6 of 868 | 1,736 | NCT00835770 | Trial comparisons |
| BG00012 240 mg BID vs BG00012 240 mg TID: serious adverse events | 279 of 868 | 272 of 868 | 1,736 | NCT00835770 | Trial comparisons |
| Active Treatment Phase: Laquinimod 0.6 mg vs Active Treatment Phase: Laquinimod 1.2 mg: Active Treatment Phase: Number of Participants With Potentially Clinically Significant Abnormal Serum Chemistry | 887 of 891 | 501 of 504 | 1,395 | NCT01707992 | Trial comparisons |
Active Treatment Phase: Laquinimod 0.6 mg vs Active Treatment Phase: Laquinimod 1.2 mg: Active Treatment Phase: Number of Participants With Potentially Clinically Significant Abnormal Hematology Values | 886 of 891 | 499 of 504 | 1,395 | NCT01707992 | Trial comparisons |
| Active Treatment Phase: Laquinimod 0.6 mg vs Active Treatment Phase: Laquinimod 1.2 mg: Active-Treatment Phase: Number of Participants With AEs | 442 of 891 | 241 of 504 | 1,395 | NCT01707992 | Trial comparisons |
| Active Treatment Phase: Laquinimod 0.6 mg vs Active Treatment Phase: Laquinimod 1.2 mg: Active-Treatment Phase: Number of Participants With Clinically Significant Vital Signs Abnormalities | 17 of 891 | 7 of 504 | 1,395 | NCT01707992 | Trial comparisons |
| IFN β-1a 30 µg (301)/DAC HYP 150 mg (303) vs DAC HYP 150 mg (301) /DAC HYP 150 mg (303): Number of Participants Who Are Free From Disease Activity in the 205MS303 Treatment Period | 9 of 597 | 7 of 606 | 1,203 | NCT01797965 | Trial comparisons |
| IFN β-1a 30 µg (301)/DAC HYP 150 mg (303) vs DAC HYP 150 mg (301) /DAC HYP 150 mg (303): Number of Participants With Relapse in the 205MS301-303 Combined Study Period | 339 of 597 | 261 of 606 | 1,203 | NCT01797965 | Trial comparisons |
1 to 10 of 277
See all 277 comparisons in its trialsPapers from its trials597
The papers the trials shown here list on ClinicalTrials.gov as their results (RESULT) or as drawn from them (DERIVED), results first, newest first.
Data dates
The date of each source this release read.
Sources 6
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ChEMBL, through Open TargetsCC BY-SA 3.0
- ClinicalTrials.govNo license stated
- NLM's MeSHNLM's terms
- Open TargetsCC0 1.0
- PubMedNLM's terms
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- ClinicalTrials.govnone stated
- NLM's MeSHNLM's
- Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- PubMedNLM's terms
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this disease from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/diseases/v1/EFO_0803536
GET https://conductscience.org/api/diseases/v1/EFO_0803536/drugs?page=2