The European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) announced on 31 January 2019 that it had recommended granting marketing authorization for the adalimumab biosimilars Idacio and Kromeya.
- INICIO
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Genéricos
Novedades
- US generics launch and approval for Dr Reddy’s and Lupin
- Five Chinese companies join UN’s MPP for Covid-19 medicines
- South Korean companies to make generic Bridion and COVID-19 drugs
- Revlimid (lenalidomide) generics launch across Europe
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Biosimilares
Novedades
- Clinical study advances for Alvotech golimumab and Dr Reddy’s rituximab biosimilars
- New insulin glargine and potential adalimumab interchangeable biosimilars
- Biosimilar advances for Alvotech-Teva and setback for Biocon Biologics
- Advances for Bio-Thera’s secukinumab and mepolizumab copy biologicals
Investigación
- Best-value biological selection making: more to consider than only price
- EE.UU. frente a Alemania y Suiza: El mercado estadounidense de biosimilares se queda atrás con precios más altos
- Drug survival of adalimumab biosimilars in psoriasis treatment in Spain
- Pegfilgrastim biosimilars in US supportive oncology
General
- US PBMs add multiple Humira biosimilars to formularies
- Canada’s Ontario introduces biosimilars switching policy
- Hechos clave en la regulación de la aprobación de biosimilares en Brasil
- La provincia canadiense de Saskatchewan introduce una política de switching de biosimilares
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