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8666 résultats correspondants
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dans le périmètre Toutes les maladies
Niveau clinique
Études et traitements 4050
Interventions, programmes et essais cliniques rattachés au périmètre sélectionné.
| Molécule / élément | Maladie / population | Objectif | Phase / stade | Statut / preuve | Mécanisme / résumé | Source | Détail |
|---|---|---|---|---|---|---|---|
| anti-CD19-CAR-T cells NCT06420154 · The Safety and Efficacy of Anti-CD19 CAR-T Cells in Patients With Relapsed/Refra… | Sclérose en plaques | Immunomodulation · Thérapie cellulaire | Phase 1 | NOT_YET_RECRUITING | This is an investigator-initiated trial to evaluate the safety and efficac… À vérifier | ClinicalTrials.gov 2026-09-20 04:37:27 | Détail |
| ASP2802 NCT06248086 · A Study to Find a Suitable Dose of ASP2802 in People With CD20-positive B-cell L… | Sclérose en plaques | Immunomodulation · Thérapie cellulaire | Phase 1 | TERMINATED | CAR-T cell therapy is a type of treatment for people with certain lymphoma… À vérifier | ClinicalTrials.gov 2026-09-20 04:37:27 | Détail |
| Bexxar NCT00434629 · Safety and Efficacy of Bexxar Therapy in the Treatment of Relapsed/Residual B-Ce… | Sclérose en plaques | À vérifier | Phase 1 | COMPLETED | Patients with B-cell lymphoma who relapse after autologous transplant tend… À vérifier | ClinicalTrials.gov 2026-09-20 04:37:27 | Détail |
| CD19/CD22 CAR-T NCT04499573 · Bispecific CD19/CD22 CAR-T for Treatment of Children and Young Adults With r/r B… | Sclérose en plaques | Thérapie cellulaire | Phase 1/2 | ACTIVE_NOT_RECRUITING | The purpose of this study is to evaluate the safety and efficiency of auto… À vérifier | ClinicalTrials.gov 2026-09-20 04:37:27 | Détail |
| cemacabtagene ansegedleucel NCT06500273 · ALPHA3 — Consolidation of First-Line MRD+ Remission With Cema-cel in Patients Wi… | Sclérose en plaques | À vérifier | Phase 2 | RECRUITING | This is a randomized, open-label study in adult patients who have complete… À vérifier | ClinicalTrials.gov 2026-09-20 04:37:27 | Détail |
| CliniMACS Cell Processing System for TCRαβ + T Cell and CD45RA Deplet… NCT03810196 · CD45RA Depleted Peripheral Stem Cell Addback for Viral or Fungal Infections Post… | Sclérose en plaques | Immunomodulation · Thérapie cellulaire | Non applicable | RECRUITING | The major morbidities of allogeneic hematopoietic stem cell transplant wit… À vérifier | ClinicalTrials.gov 2026-09-20 04:37:27 | Détail |
| KYV-101, an autologous fully-human anti-CD19 CAR T-cell immunotherapy NCT06590545 · IDEAL — Anti-CD 19 CAR-T Cell Therapy in Patients With ANCA Vasculitis | Sclérose en plaques | Thérapie cellulaire | Phase 1/2 | NOT_YET_RECRUITING | The goal of this phase I/II clinical trial is to investigate anti-CD 19 ch… À vérifier | ClinicalTrials.gov 2026-09-20 04:37:27 | Détail |
| rapcabtagene autoleucel (YTB323) NCT07443137 · CAR-T ceLL for Eradication of Active Residual Disease in LBCL (CLEAR-1 Study) | Sclérose en plaques | Immunomodulation · Thérapie cellulaire | Phase 1 | NOT_YET_RECRUITING | This is an open-label, multi-center, non-confirmatory study to assess the… À vérifier | ClinicalTrials.gov 2026-09-20 04:37:27 | Détail |
| rondecabtagene autoleucel NCT07188558 · PiNACLE-H2H — A Study to Investigate Ronde-cel Versus Investigator's Choice CD19… | Sclérose en plaques | Immunomodulation · Thérapie cellulaire | Phase 3 | RECRUITING | This Phase 3 study compares rondecabtagene autoleucel (ronde-cel), a dual-… À vérifier | ClinicalTrials.gov 2026-09-20 04:37:27 | Détail |
| TC011 single-arm NCT07360288 · TC011_FL_201 — Efficacy and Safety of TC011 in Relapsed or Refractory Follicular… | Sclérose en plaques | Thérapie cellulaire | Phase 2 | NOT_YET_RECRUITING | This Phase II, multi-center, single-arm, open-label study evaluates the ef… À vérifier | ClinicalTrials.gov 2026-09-20 04:37:27 | Détail |
| ThisCART19A with Dose Level 1 NCT05691153 · ThisCART19A for B-NHL Relapsed After Auto-CAR T | Sclérose en plaques | Thérapie cellulaire | Phase 1 | UNKNOWN | This is a phase 1, single-center, dose selection study to evaluate the eff… À vérifier | ClinicalTrials.gov 2026-09-20 04:37:27 | Détail |
| Rituximab NCT03636503 · Rituximab + Immunotherapy in Follicular Lymphoma | Sclérose en plaques | À vérifier | Phase 1 | TERMINATED | The primary objective of this phase III trial is to investigate if Rituxim… À vérifier | ClinicalTrials.gov 2026-09-20 04:37:26 | Détail |
| Rituximab NCT00006669 · Rituximab Followed by Combination Chemotherapy in Treating Patients With Refract… | Sclérose en plaques | À vérifier | Phase 2 | WITHDRAWN | The primary objective of this phase III trial is to investigate if Rituxim… À vérifier | ClinicalTrials.gov 2026-09-20 04:37:26 | Détail |
| SCT400 plus CHOP NCT02772822 · A Study Comparing the Efficiency and Safety of S-CHOP(Cyclophosphamide, Hydroxyd… | Sclérose en plaques | Immunomodulation | Phase 3 | UNKNOWN | The primary objective of the study is to assess the efficiency of SCT400 p… À vérifier | ClinicalTrials.gov 2026-09-20 04:37:26 | Détail |
| Armored and GPC3-targeted autologous CAR T-cell NCT06590246 · A Study to Evaluate C-CAR031 in Glypican-3 (GPC3)+ Advanced/Recurrent Hepatocell… | Sclérose en plaques | À vérifier | Phase 1/2 | RECRUITING | This single-arm, open-label multicenter Phase I/II study will evaluate the… À vérifier | ClinicalTrials.gov 2026-09-20 04:37:25 | Détail |
| C-CAR031 NCT05155189 · A Study to Evaluate Safety and Efficacy of Armored CAR-T Cell Injection C-CAR031… | Sclérose en plaques | Immunomodulation · Thérapie cellulaire | Phase 1 | RECRUITING | A study that aimed to assess the safety and anti-tumor activity of CCAR031… À vérifier | ClinicalTrials.gov 2026-09-20 04:37:25 | Détail |
| C-CAR031 NCT07444281 · An Phase I Trial of a CAR T-cell Infusion C-CAR031 in Participants With GPC3+ Ad… | Sclérose en plaques | À vérifier | Phase 1 | RECRUITING | A study that aimed to assess the safety and anti-tumor activity of CCAR031… À vérifier | ClinicalTrials.gov 2026-09-20 04:37:25 | Détail |
| CD19/CD20-directed Chimeric Antigen Receptor T Cells NCT05149391 · A Study of C-CAR039 in Subjects With Relapsed and/or Refractory B Cell Non-Hodgk… | Sclérose en plaques | Immunomodulation | Phase 1 | COMPLETED | This is a single-center, open-label study to evaluate the safety and effic… À vérifier | ClinicalTrials.gov 2026-09-20 04:37:25 | Détail |
| Prizloncabtagene Autoleucel NCT04317885 · A Study Evaluating Safety and Efficacy of C-CAR039 Treatment in NHL Subjects | Sclérose en plaques | À vérifier | Phase 1 | COMPLETED | The trial is a single arm, single-center, non-randomized phase I clinical… À vérifier | ClinicalTrials.gov 2026-09-20 04:37:25 | Détail |
| Prizloncabtagene Autoleucel NCT04693676 · A Study of C-CAR039 Treatment in Subjects With r/r NHL Subjects Non-Hodgkin's Ly… | Sclérose en plaques | À vérifier | Phase 1 | UNKNOWN | The trial is a single arm, single-center, non-randomized phase I clinical… À vérifier | ClinicalTrials.gov 2026-09-20 04:37:25 | 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. | |||||||