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[Evolution of biologicals in inflammation medicine--biosimilars in gastroenterology, rheumatology and dermatology].
- Source :
-
Deutsche medizinische Wochenschrift (1946) [Dtsch Med Wochenschr] 2014 Nov; Vol. 139 (47), pp. 2399-404. Date of Electronic Publication: 2014 Nov 12. - Publication Year :
- 2014
-
Abstract
- Biologicals revolutionized the therapy of chronic inflammatory diseases in gastroenterology, rheumatology and dermatology in the last decade. The first generation biologicals mainly targeted against the pro-inflammatory cytokine TNF-α. The evolution of these therapies in the last years led to the development of new antibodies and to the admission of first generation "generic" biologics - the biosimilars. Biosimilars are not a fundamental new pharmacological development for existing substances, however they have the potential to lead to enormous cost savings in healthcare without reducing the level of care for patients. Biosimilars are not identical with the originator, but in an extensive biosimilarity exercise including analytical, preclinical and comparative clinical studies it was shown that the biosimilars could demonstrate comparability in all relevant aspects with the originator.In September 2013, the Infliximab biosimilars (Inflectra(®), Remsina(®)) were the first biosimilars for monoclonal antibodies to be authorized by the EMA for use in the European Union. By demonstrating the therapeutic similarity only in one indication (rheumatoid arthritis) the EMA agreed with an extrapolation also to all approved indications of the originator. This could be a relevant problem in clinical practice. Therefore, comparative studies with the originator are required in all approved indications.After expiration of the national patent protection in beginning of 2015, the infliximab biosimilars will be launched on the market in Germany and will be part of the therapeutic arsenal in gastroenterology, rheumatology and dermatology. Interchangeability (Switching) of biosimilars with the originator will be subject of an important discussion with the health care providers. Regardless of the biosimilars EMA-approval, several potential problems (efficacy, extrapolation, switching, long-term safety) should be the topic of intensive long-term registries in the future.<br /> (© Georg Thieme Verlag KG Stuttgart · New York.)
- Subjects :
- Antibodies, Monoclonal adverse effects
Antibodies, Monoclonal economics
Antibodies, Monoclonal therapeutic use
Arthritis, Rheumatoid drug therapy
Arthritis, Rheumatoid economics
Arthritis, Rheumatoid immunology
Biological Products adverse effects
Biological Products economics
Biosimilar Pharmaceuticals adverse effects
Biosimilar Pharmaceuticals economics
Cost Savings
Drug Approval
European Union
Gastrointestinal Diseases economics
Gastrointestinal Diseases immunology
Germany
Humans
Inflammation drug therapy
Inflammation economics
Inflammation immunology
Infliximab
National Health Programs economics
Patents as Topic
Rheumatic Diseases economics
Rheumatic Diseases immunology
Skin Diseases economics
Skin Diseases immunology
Therapeutic Equivalency
Tumor Necrosis Factor-alpha antagonists & inhibitors
Biological Products therapeutic use
Biosimilar Pharmaceuticals therapeutic use
Gastrointestinal Diseases drug therapy
Rheumatic Diseases drug therapy
Skin Diseases drug therapy
Subjects
Details
- Language :
- German
- ISSN :
- 1439-4413
- Volume :
- 139
- Issue :
- 47
- Database :
- MEDLINE
- Journal :
- Deutsche medizinische Wochenschrift (1946)
- Publication Type :
- Academic Journal
- Accession number :
- 25390629
- Full Text :
- https://doi.org/10.1055/s-0034-1387371