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Traitements, essais et publications liés.
Traitements5programmes
Essais2liés
Publications4liées
SourceDBlocale
Traitements
5| Molécule | Indication / population | Phase | Objectif | Pays | Résultat |
|---|---|---|---|---|---|
| BCD-063The objective of the clinical study of the medicinal product for medical use: to compare efficacy and safety of the generic drug BCD-063 and Copaxone®-Teva in patients with relapsing-remitting multiple sclerosis. Period of the clinical study of the medicinal product for medical use: from June 10, 2013 to March 23, 2016. Number of patients, involved into the study of the medicinal product for medical use: 158 patients. | SEP | Phase 3 | Neuroprotection | À vérifier | |
| BCD-281The aim of this study is to compare the efficacy, safety profile, pharmacokinetics, pharmacodynamics, and immunogenicity of BCD-281 and the reference drug in subjects with relapsing multiple sclerosis. | SEP | Phase 3 | À vérifier | Russia | À vérifier |
| Copaxone-TevaThe objective of the clinical study of the medicinal product for medical use: to compare efficacy and safety of the generic drug BCD-063 and Copaxone®-Teva in patients with relapsing-remitting multiple sclerosis. Period of the clinical study of the medicinal product for medical use: from June 10, 2013 to March 23, 2016. Number of patients, involved into the study of the medicinal product for medical use: 158 patients. | SEP | Phase 3 | Neuroprotection | À vérifier | |
| BCD-063The objective of the clinical study of the medicinal product for medical use: to compare efficacy and safety of the generic drug BCD-063 and Copaxone®-Teva in patients with relapsing-remitting multiple sclerosis. Period of the clinical study of the medicinal product for medical use: from June 10, 2013 to March 23, 2016. Number of patients, involved into the study of the medicinal product for medical use: 158 patients. | SEP | Phase 3 | Neuroprotection | À vérifier | |
| BCD-281The aim of this study is to compare the efficacy, safety profile, pharmacokinetics, pharmacodynamics, and immunogenicity of BCD-281 and the reference drug in subjects with relapsing multiple sclerosis. | SEP | Phase 3 | À vérifier | Russia | À vérifier |
Essais cliniques
2| Molécule | Indication / population | Phase | NCT | Titre | Statut |
|---|---|---|---|---|---|
| BCD-281 | SEP | Phase 3 | NCT07321093 | MUSCAT — A Study of the Efficacy and Safety of BCD-281 in Patients With Relapsing-Remitting Multiple Sclerosis | RECRUITING |
| BCD-063 | SEP | Phase 3 | NCT02753088 | Efficacy and Safety of BCD-063 and Copaxone-Teva in Patients With Relapsing-Remitting Multiple Sclerosis | COMPLETED |
Publications
4| Molécule | Indication / population | Titre | Journal | Date |
|---|---|---|---|---|
| Copaxone-Teva | Higher satisfaction and adherence with glatiramer acetate 40 mg/mL TIW vs 20 mg/mL QD in RRMS. | Multiple sclerosis and related disorders | ||
| Copaxone-Teva | Physicochemical and Biological Examination of Two Glatiramer Acetate Products. | Biomedicines | ||
| Copaxone-Teva | The influence of glatiramer acetate on Th17-immune response in multiple sclerosis. | PloS one | ||
| BCD-063 | [Comparative, placebo-controlled clinical study of efficacy and safety of glatiramer acetate 20 mg in patients with relapsing-remitting multiple sclerosis: results of the first year of the study]. | Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova |