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Biosimilar Market Report – Healthcare Economist

Samsung Bioepis has a Biosimilar Market Report for Q2 2024. Some key highlights:

  • As of April 2024, the FDA has authorised a complete of 48 biosimilars throughout 15 distinctive organic molecules.  Of the 48 approvals, 38 biosimilars have launched within the US market.   In Q2 2024, 3 new biosimilars have been authorised within the US (Simlandi for Humira (adalimumab); Jubbonti/Wyost for Prolia/Xgeva (denosumab); Tyenne for Actemra (tocilizumab))
  • Average reductions. Total, biosimilars are resulting in decrease costs, largely by rebates fairly than record worth. Nevertheless, costs fell by 41% inside 3 years with a variety of variability throughout therapeutic areas.
    • In oncology, biosimilars wholesale acquisition value (WAC) costs have been 10%-25% decrease than reference merchandise. In supportive care,
    • For supportive care, WAC costs of biosimilars for pegfilgrastim and epoetin alfa are 20-60% decrease reference, however common gross sales costs (ASP) for the reference merchandise has fallen to match ASP for biosimilars in an effort to retain market share.
    • Immunology (Infliximab). Infliximab biosimilars launched with progressively decrease WACs, starting from -19% to -59% in reductions. Biosimilar competitors has led to ASP costs 75-90% decrease than the reference product WAC
    • Immunology (Humira). Adalimumab (Humira) biosimilars have taken totally different approaches. Two biosimilars have used decrease WAC costs (85% reductions). Most Infliximab biosimilars launched with progressively decrease WACs, starting from -19% to -59% in reductions. Biosimilar competitors has led to ASP costs 75-90% decrease than the reference product WAC
    • Opthalmology. Current ranibizumab (Lucentis) biosimilar launches have already led to 30-40% decrease reference product ASP prices. Six different biosimilars have used an method with comparable WAC costs to branded Humira however with massive rebates the scale back costs by 55%-90% of the reference product.
    • Diabetes. Biosimilars for Lantus (insulin glargin) have additionally used a combined method the place some merchandise have decrease WAC and others have comparable WAC however decrease costs resulting from rebates.
  • Biosimilar uptake varies by molecule. Three years post-launch, biosimilar uptake for bevacizumab, trastuzumab, pegfilgrastm and rituximab have been all >50%. For different medicine equivalent to insulin glargine, epoetin alfa and infliximab, market shares have been all <50% at yr 3. On the whole, market share rises considerably over time, nonetheless, in immunology Humira branded merchandise nonetheless comprise 96% market share.
  • Inflation Discount Act. There are some provisions which might be constructive for biosimilars and others much less so.
    • Professional: Lack of producer income from Medicare Drug Value Negotiation and Inflation Rebate could lead producers to launch with increased record costs and/or scale back rebate charges in different therapeutic areas or strains of enterprise (e.g. personal insurance coverage). Biosimilars could provide higher value aid in these future markets. Moreover, the elevated Medicare fee restrict for biosimilars to ASP + 8% helps offset a number of the losses that suppliers could incur when utilizing cheaper ASP biosimilars on the medical profit
    • Con: Medicare Drug Value Negotiation will impose pricing strain on the chosen medicine and their related rivals. In these markets (i.e. Enbrel, Stelara), the financial savings that biosimilars can provide to plans could also be decreased, making step remedy by biosimilars a much less enticing technique for plan sponsors to implement. Furthermore, reductions and caps within the Half D member value sharing necessities, whereas a constructive enchancment for the general affordability of Medicare beneficiaries, unintentionally reduces the monetary incentive for members to change to a biosimilar from an originator product

You may learn the total deck right here.


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