South Korean biotechnology company Celltrion announced two new data sets on the subcutaneous formulation Remsima (infliximab) in a number of conditions in March 2022. This followed the February 2022 announcement that the high-concentration version of Celltrion’s autoimmune disease biosimilar Yuflyma (adalimumab) has received approval from the European Commission.
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- Consequences of generics being favoured by healthcare providers
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- FDA approves pegfilgrastim and rituximab biosimilars
- Byooviz: first ophthalmology biosimilar launches in US
- Biocon: cancer biosimilar launch in Canada and US$90 million Malaysia deal
- Canada approves five biosimilars in last seven months
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- El impacto de las insulinas biosimilares en el gasto público brasileño
- Challenges with implementing benefit-sharing programmes for biologicals in Europe
- Successful increase of biosimilar adoption in a large integrated health delivery network
- Estado actual de los biosimilares de anticuerpos monoclonales aprobados en América Latina
- Una visión general de los biosimilares de anticuerpos monoclonales en América Latina
- American Academy of Ophthalmology biosimilars position statement published
- US prescription drug expenditure projection report
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