Vue transversale globale
Toutes les maladies
Un même point d’entrée pour les études cliniques, les découvertes scientifiques, les publications et les pistes exploratoires présentes dans Biomedical Watch.
Périmètre
Filtrer toute la vue
Chaque choix s’applique immédiatement aux quatre sections. Le filtre « type de SEP » n’apparaît que lorsque la sclérose en plaques est sélectionnée.
8841 résultats correspondants
· 41 visibles sur cette page
dans le périmètre Toutes les maladies
Niveau clinique
Études et traitements 4225
Interventions, programmes et essais cliniques rattachés au périmètre sélectionné.
| Molécule / élément | Maladie / population | Objectif | Phase / stade | Statut / preuve | Mécanisme / résumé | Source | Détail |
|---|---|---|---|---|---|---|---|
| anti-CD19/BCMA CAR NK cells NCT06926985 · An Exploratory Clinical Study of Anti-CD19/BCMA Chimeric Antigen Receptor NK Cel… | Sclérose en plaques | À vérifier | Phase 1 | WITHDRAWN | A single arm, open-label pilot study is designed to evaluate the safety an… À vérifier | ClinicalTrials.gov 2026-09-27 04:37:36 | Détail |
| IBI301 NCT02945215 · A Study to Assess the Pharmacokinetics and Safety of Recombinant Human Murine Ch… | Sclérose en plaques | Immunomodulation | Phase 1 | COMPLETED | Randomised, double-blind, parallel group study to compare PK and PD profil… À vérifier | ClinicalTrials.gov 2026-09-27 04:37:36 | Détail |
| Tislelizumab NCT06167785 · ZeTA — A Study to Evaluate Zanubrutinib and Tislelizumab in Progressive Lymphoma… | Sclérose en plaques | Thérapie cellulaire | Phase 2 | RECRUITING | The current standard of care for locally advanced non-small cell lung canc… À vérifier | ClinicalTrials.gov 2026-09-27 04:37:36 | Détail |
| Biospecimen Collection NCT03984448 · Testing the Addition of a New Anti-cancer Drug, Venetoclax, to Usual Chemotherap… | Sclérose en plaques | À vérifier | Phase 2/3 | ACTIVE_NOT_RECRUITING | This phase III trial compares standard of care hormone therapy plus riboci… À vérifier | ClinicalTrials.gov 2026-09-27 04:37:35 | Détail |
| F520+F007 NCT05178836 · A Phase II Study to Evaluate the Efficacy and Safety of F520 Combined With F007… | Sclérose en plaques | À vérifier | Phase 2 | UNKNOWN | This is an open-label, single-arm, and multicenter phase Ⅱ study designed… À vérifier | ClinicalTrials.gov 2026-09-27 04:37:35 | Détail |
| Abiraterone acetate NCT01017939 · A Drug-Drug Interaction Study of Abiraterone Acetate Plus Prednisone With Dextro… | Sclérose en plaques | Ralentissement de la progression · Thérapie génique | Phase 1 | COMPLETED | The purpose of this study is to assess the efficacy and safety of opevesos… À vérifier | ClinicalTrials.gov 2026-09-27 04:37:30 | Détail |
| Aminophylline NCT01240824 · Study of BCG + Aminophylline Toxicity When Used in the Treatment of Bladder Canc… | Sclérose en plaques | Traitement symptomatique | Phase 1 | COMPLETED | This safety study is the first in a series of studies testing the applicat… À vérifier | ClinicalTrials.gov 2026-09-27 04:37:30 | Détail |
| Aminophylline NCT04151381 · The Effect of Preoperative Aminophylline | Sclérose en plaques | À vérifier | Phase 1 | UNKNOWN | This safety study is the first in a series of studies testing the applicat… À vérifier | ClinicalTrials.gov 2026-09-27 04:37:30 | Détail |
| Inj Aminophylline 100mg with Inj Acetaminophen 1000mg in 100ml Normal… NCT07528118 · Comparison of Acetaminophen With Aminophylline and Aminophylline With Dexamethas… | Sclérose en plaques | À vérifier | Phase 2 | COMPLETED | It is hypothesized that there is a difference between intravenously admini… À vérifier | ClinicalTrials.gov 2026-09-27 04:37:30 | Détail |
| LABA based treatment: indacaterol NCT01794780 · A 1-year Multi-center, Prospective, Cohort Study in Patients With Chronic Obstru… | Sclérose en plaques | À vérifier | Phase 4 | COMPLETED | This multi-center study is designed to describe natural history of disease… À vérifier | ClinicalTrials.gov 2026-09-27 04:37:30 | Détail |
| Theophylline NCT02340520 · Enhancement of Corticosteroid Efficacy in COPD | Sclérose en plaques | À vérifier | Phase 3 | COMPLETED | To evaluate the effect of multiple doses of BIIL 284 BS on the pharmacokin… À vérifier | ClinicalTrials.gov 2026-09-27 04:37:30 | Détail |
| Theophylline NCT04551170 · Theophylline Treatment for Pseudohypoparathyroidism - Children 2-12 Years Old | Sclérose en plaques | À vérifier | Phase 2 | ACTIVE_NOT_RECRUITING | To evaluate the effect of multiple doses of BIIL 284 BS on the pharmacokin… À vérifier | ClinicalTrials.gov 2026-09-27 04:37:30 | Détail |
| deferiprone NCT02880033 · LymphoEnergy — Oxidative Stress and Apoptosis of Energy Metabolism by Deferipron… | Sclérose latérale amyotrophique | Neuroprotection | Non applicable | COMPLETED | Description non affichée : incohérence de maladie détectée. Consultez l’es… À vérifier | ClinicalTrials.gov 2026-09-27 04:37:16 | Détail |
| ALT001 1.0 μg/kg NCT07833618 · A Phase II Study of ALT001 in Patients With Amyotrophic Lateral Sclerosis (ALS) | Sclérose latérale amyotrophique | Thérapie cellulaire | Phase 2 | NOT_YET_RECRUITING | Description non affichée : incohérence de maladie détectée. Consultez l’es… À vérifier | ClinicalTrials.gov 2026-09-27 04:37:15 | Détail |
| B cell infusion NCT07838389 · Evaluation of Donor-Derived B Cell Infusions in Patients With Amyotrophic Latera… | Sclérose latérale amyotrophique | Immunomodulation | Phase 1 | NOT_YET_RECRUITING | Description non affichée : incohérence de maladie détectée. Consultez l’es… À vérifier | ClinicalTrials.gov 2026-09-27 04:37:15 | Détail |
| Cyclophosphamide NCT07834450 · CORTEX-ALS — Efficacy and Safety of Cyclophosphamide in Amyotrophic Lateral Scle… | Sclérose latérale amyotrophique | À vérifier | Phase 2 | NOT_YET_RECRUITING | This randomized phase II trial studies how well paclitaxel with or without… À vérifier | ClinicalTrials.gov 2026-09-27 04:37:15 | Détail |
| Dazucorilant 300 mg NCT05407324 · DAZALS — Dazucorilant in Patients With Amyotrophic Lateral Sclerosis | Sclérose latérale amyotrophique | À vérifier | Phase 2 | ACTIVE_NOT_RECRUITING | Description non affichée : incohérence de maladie détectée. Consultez l’es… À vérifier | ClinicalTrials.gov 2026-09-27 04:37:15 | Détail |
| High-tech rehabilitative treatment NCT06881979 · Fit4MR-ChrMND — High-Tech Rehabilitation Pathway for Chronic Adult Neuromuscular… | Sclérose latérale amyotrophique | Traitement symptomatique | Non applicable | RECRUITING | The primary objective is to demonstrate, in a population of chronic neurom… À vérifier | ClinicalTrials.gov 2026-09-27 04:37:15 | Détail |
| Long term mechanical ventilation support NCT05744310 · ALS-LTMV — Effects of Long Term Ventilation Support on the Quality of Life of AL… | Sclérose latérale amyotrophique | À vérifier | Non applicable | RECRUITING | Description non affichée : incohérence de maladie détectée. Consultez l’es… À vérifier | ClinicalTrials.gov 2026-09-27 04:37:15 | Détail |
| neck exoskeleton controller NCT07836751 · Using Gaze to Enable Head-neck Movements in Patients With Head Drop | Sclérose latérale amyotrophique | Traitement symptomatique | Non applicable | RECRUITING | Description non affichée : incohérence de maladie détectée. Consultez l’es… À vérifier | ClinicalTrials.gov 2026-09-27 04:37:15 | Détail |
Découverte scientifique
Recherches et trouvailles 21
Projets précliniques, publications émergentes et programmes de recherche suivis dans le pipeline.
| Molécule / élément | Maladie / population | Objectif | Phase / stade | Statut / preuve | Mécanisme / résumé | Source | Détail |
|---|---|---|---|---|---|---|---|
| 4-octyl itaconate et dérivés Dérivés de l’itaconate — neuroinflammation | Sclérose latérale amyotrophique | Neuroprotection · Immunomodulation | Découverte fondamentale | Exploratoire | Modulation immunométabolique de la microglie · NRF2 / inflammation microgl… Piste mécanistique visant à reprogrammer la réponse inflammatoire de la microglie. Le lien avec la SLA reste exploratoi… | Revue scientifique 2024-07-01 | Détail |
Bibliographie
Publications 4595
Références bibliographiques de la base locale et accès à leur source originale.
| Molécule / élément | Maladie / population | Objectif | Phase / stade | Statut / preuve | Mécanisme / résumé | Source | Détail |
|---|---|---|---|---|---|---|---|
| AAV microdystrophin gene replacement therapy for Duchenne muscular dy… PF-06939926 · PMID 40817386 | Myopathies | Thérapie cellulaire · Thérapie génique | Publication | PubMed | Voir la publication source Duchenne muscular dystrophy (DMD) is caused by pathogenic sequence variants occurring in the DMD gene which lead to the… | Gene therapy 2026-08-13 15:03:50 | Source |
| Cardiac safety of fordadistrogene movaparvovec gene therapy in Duchen… PF-06939926 · PMID 40583273 | Myopathies | Ralentissement de la progression · Thérapie génique | Publication | PubMed | Voir la publication source Fordadistrogene movaparvovec (FM; PF-06939926) is a recombinant adeno-associated virus serotype-9 gene-replacement cons… | Molecular therapy : the journal of the American Societ… 2026-08-13 15:03:50 | Source |
| An Antibody-Oligonucleotide Conjugate for Myotonic Dystrophy Type 1. Del-desiran (AOC 1001) · PMID 41707138 | Myopathies | Thérapie génique | Publication | PubMed | Voir la publication source Myotonic dystrophy type 1 is a rare, dominantly inherited, progressive, disabling, neuromuscular disease that leads to… | The New England journal of medicine 2026-08-13 15:03:49 | Source |
| Effect of using knee extension aid for gait training in subacute hemi… Extension assist knee ankle foot orthosis (EA-KAFO) · PMID 42544336 | Myopathies | À vérifier | Publication | PubMed | Voir la publication source [Purpose] In normal gait, the knee flexes approximately 60° during the swing phase, and the lower leg's inertial force… | Journal of physical therapy science 2026-08-13 15:03:49 | Source |
| Robot-Assisted Gait Training to Improve Gait Patterns in Two Adolesce… Extension assist knee ankle foot orthosis (EA-KAFO) · PMID 41332284 | Myopathies | À vérifier | Publication | PubMed | Voir la publication source Although the effectiveness of robot-assisted gait training (RAGT) in stroke has been reported, evidence in adolescents… | Physical & occupational therapy in pediatrics 2026-08-13 15:03:49 | Source |
| BMN 351-Induced Exon Skipping and Dystrophin Expression in Skeletal a… BMN 351 · PMID 39916519 | Myopathies | Thérapie génique | Publication | PubMed | Voir la publication source Duchenne muscular dystrophy (DMD) is caused by mutations of the gene that prevent the expression of functional dystroph… | Nucleic acid therapeutics 2026-08-13 15:03:48 | Source |
| Targeting a Novel Site in Exon 51 with Antisense Oligonucleotides Ind… BMN 351 · PMID 39916530 | Myopathies | Thérapie génique | Publication | PubMed | Voir la publication source Exon skipping with antisense oligonucleotides (ASOs) can correct disease-causing mutations of Duchenne muscular dystrop… | Nucleic acid therapeutics 2026-08-13 15:03:48 | Source |
| From design to clinic: Medicinal chemistry and pharmacology of approv… Givinostat · PMID 42546588 | Cancer | À vérifier | Publication | PubMed | Voir la publication source Many diseases, including cancer, are characterized by increased or decreased expression of specific genes. These change… | European journal of medicinal chemistry 2026-08-13 15:03:47 | Source |
| Real-world safety profile of givinostat: an early post-marketing phar… Givinostat · PMID 42494524 | Myopathies | Ralentissement de la progression | Publication | PubMed | Voir la publication source Givinostat is a novel histone deacetylase inhibitor, which was approved by the US Food and Drug Administration (FDA) in… | Frontiers in pharmacology 2026-08-13 15:03:47 | Source |
| Bone marrow mesenchymal stem cell exosomes in osteonecrosis: patholog… Human Umbilical Cord Mesenchymal Stem Cells (UC-MSC) · PMID 42550377 | Myopathies | Traitement symptomatique · Thérapie cellulaire | Publication | PubMed | Voir la publication source Osteonecrosis is bone death caused by disrupted blood supply. It often leads to bone collapse and joint failure. Curren… | Molecular biology reports 2026-08-13 15:03:46 | Source |
| Subconjunctival Injection of Mesenchymal Stem Cells for Corneal Wound… Human Umbilical Cord Mesenchymal Stem Cells (UC-MSC) · PMID 42454124 | Myopathies | Immunomodulation · Thérapie cellulaire | Publication | PubMed | Voir la publication source Previous studies in animal models have demonstrated that mesenchymal stem cells (MSCs) are beneficial for reconstructin… | Frontiers in medicine 2026-08-13 15:03:46 | Source |
| Development of a DUX4-targeting antibody oligonucleotide conjugate as… AOC-1020 · PMID 41994867 | Myopathies | Thérapie génique | Publication | PubMed | Voir la publication source Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant muscular disease in which genetic mutations acti… | Nucleic acids research 2026-08-13 15:03:45 | Source |
| Preclinical evaluation of INS1201 AAV9-micro-dystrophin via CSF admin… INS1201 · PMID 42137291 | Myopathies | Immunomodulation | Publication | PubMed | Voir la publication source INS1201 is an investigational adeno-associated virus 9-micro-dystrophin gene transfer therapy under development as a po… | Molecular therapy. Advances 2026-08-13 15:03:44 | Source |
| Characterization of two DNase gamma-specific monoclonal antibodies an… HG302 · PMID 10964668 | Myopathies | À vérifier | Publication | PubMed | Voir la publication source Two novel monoclonal antibodies (mAbs), hg302 and hg303, raised against a synthetic peptide corresponding to the basic… | Biochemical and biophysical research communications 2026-08-13 15:03:36 | Source |
| Integrated Genotyping Strategies for Uncovering Detailed Haplotype St… Study of Genotype and Phenotype Characterization in Duchenne Muscular Dystrophy With Small Mut… | Myopathies | À vérifier | Publication | PubMed | Voir la publication source Duchenne and Becker muscular dystrophies are X-linked neuromuscular disorders caused by mutations in the dystrophin gen… | Clinical chemistry 2026-08-13 15:03:35 | Source |
| Spectrum of DMD gene mutations in 507 patients: a retrospective genot… Study of Genotype and Phenotype Characterization in Duchenne Muscular Dystrophy With Small Mut… | Myopathies | À vérifier | Publication | PubMed | Voir la publication source Duchenne muscular dystrophy (DMD) is caused by mutations in the DMD gene, but comprehensive analyses of mutational patt… | Archives de pediatrie : organe officiel de la Societe… 2026-08-13 15:03:35 | Source |
| Multivoxel proton magnetic resonance spectroscopy in facioscapulohume… Magnetic Resonance Imaging and Spectroscopy Biomarkers for Facioscapulohumeral Muscular Dystro… | Myopathies | À vérifier | Publication | PubMed | Voir la publication source Facioscapulohumeral muscular dystrophy (FSHD) is a hereditary disorder that causes progressive muscle wasting. This stu… | Muscle & nerve 2026-08-13 15:03:34 | Source |
| The magnetic resonance imaging spectrum of facioscapulohumeral muscul… Magnetic Resonance Imaging and Spectroscopy Biomarkers for Facioscapulohumeral Muscular Dystro… | Myopathies | À vérifier | Publication | PubMed | Voir la publication source Facioscapulohumeral muscular dystrophy (FSHD) is associated with a repeat contraction in the D4Z4 gene locus on chromos… | Muscle & nerve 2026-08-13 15:03:34 | Source |
| YOOMI: Effect of AI-Guided Gamified Physical Therapy Exercise Softwar… Yoomi Physical Therapy Software · PMID 41569231 | Myopathies | À vérifier | Publication | PubMed | Voir la publication source Résumé non disponible dans la base locale. | Journal of the American Geriatrics Society 2026-08-13 15:03:32 | Source |
| High Levels of (Un)Switched Memory B Cells Are Associated With Better… INFLAME-BANK — Inflammatory Disease Biobank for Immunophenotyping and Cardiovascular Research… | Myopathies | Immunomodulation | Publication | PubMed | Voir la publication source Atherosclerosis is an inflammatory lipid disorder and the main underlying pathology of acute ischemic events. Despite a… | Journal of the American Heart Association 2026-08-13 15:03:30 | Source |
Exploration — prudence
Pistes exploratoires 0
Rapprochements mécanistiques et hypothèses de recherche : ils ne constituent pas une preuve d’efficacité ni une recommandation thérapeutique.
Hypothèses non validéesÀ confirmer par des travaux précliniques, cliniques et une revue scientifique indépendante.
| Molécule / élément | Maladie / population | Objectif | Phase / stade | Statut / preuve | Mécanisme / résumé | Source | Détail |
|---|---|---|---|---|---|---|---|
| Aucune piste exploratoire ne correspond aux filtres. | |||||||