Samsung Bioepis launches Hadlima in Australia and Canada

Biosimilars/News | Posted 07/05/2021 post-comment0 Post your comment

Korea-based Samsung Bioepis (Samsung and Biogen’s joint venture) announced on 29 March 2021 that it had now launched its adalimumab biosimilar, Hadlima (SB5), in Australia and Canada.


Hadlima is a biosimilar to AbbVie’s Humira (adalimumab), which had worldwide sales of US$18.4 billion in 2017. Adalimumab is a human monoclonal antibody that treats autoimmune diseases by inhibiting tumour necrosis factor (TNF), a soluble inflammatory cytokine. Adalimumab binds to TNF-alpha (TNF-α), preventing it from activating TNF receptors, which cause the inflammatory reactions associated with autoimmune diseases. Adalimumab is indicated for the treatment of rheumatoid, juvenile idiopathic and psoriatic arthritis, ankylosing spondylitis, Crohn’s disease, psoriasis and ulcerative colitis.

Hadlima received approval from Australia’s drug regulatory body, the Therapeutic Goods Administration (TGA), in January 2018. It is the third biosimilar Samsung Bioepis has launched in Australia. The company also markets an etanercept biosimilar, Brenzys, and an infliximab biosimilar, Renflexis, in the country, which received approval from the TGA in 2016 and 2017, respectively [1].

Hadlima was listed on the Australian Pharmaceutical Benefits Scheme (PBS) on 1 April 2021, along with three other adalimumab biosimilars, Amgevita, Hyrimoz and Idacio. Under the PBS, the Australian Government subsidizes the cost of medicine for most medical conditions.

Australia’s PBS is encouraging the use of biosimilars with its Biosimilar Awareness Initiative, which is intended to support awareness of, and confidence in, the use of biosimilar medicines for healthcare professionals and consumers. The Australian Government is also implementing two specific drivers to encourage the use of biosimilar medicines, which it believes will complement the Biosimilar Awareness Initiative. The two specific biosimilar uptake drivers being implemented are:

  • encouraging prescribing of a biosimilar brand rather than the reference biological brand for treatment naïve patients.
  • providing for a simpler and faster approval process for prescribing biosimilar brands, e.g. streamlined authority, while maintaining an existing higher level authority requirement for the reference biological brand, e.g. written authority.

Samsung Bioepis says that Hadlima is now available in three markets: Europe, Canada and Australia. It was first launched in Europe in October 2018 under the name Imraldi in partnership with Biogen. Then in February 2021 it was launched in Canada in partnership with Merck (known as MSD outside of the US and Canada). The company also received approval for Hadlima from the US Food and Drug Administration in July 2019 [2].

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To further enhance the objectives of GaBI in sharing information and knowledge that ensure policies supportive of safe biosimilars use, we are pleased to announce that we will be launching a new section on GaBI Online and GaBI Journal, the ‘Latin American Forum’ (in Spanish) featuring the latest news and updates on research and developments in generic and biosimilar medicines in Latin America.

Register to receive the GaBI Latin American Forum newsletter. Inform colleagues and friends of this new initiative.



Para fomentar los objetivos de GaBI sobre la difusión de información y conocimiento sobre las políticas de apoyo que garantizan el uso seguro de medicamentos biosimilares, nos complace anunciar el lanzamiento de una nueva sección en GaBI Online y GaBI Journal, el ‘Latin American Forum’ (en español), que presentará las últimas noticias y actualizaciones en investigación y desarrollo sobre medicamentos genéricos y biosimilares en Latinoamérica.

Regístrese para recibir el boletín informativo GaBI Latin American Forum. Informe a colegas y amigos sobre esta nueva iniciativa. 

1. GaBI Online - Generics and Biosimilars Initiative. Biosimilars approved in Australia []. Mol, Belgium: Pro Pharma Communications International; [cited 2021 May 7]. Available from: 
2. GaBI Online - Generics and Biosimilars Initiative. FDA approves adalimumab biosimilar Hadlima []. Mol, Belgium: Pro Pharma Communications International; [cited 2021May 7]. Available from:

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Source: Samsung Bioepis

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