Recall that Merck's single largest retained geography on this franchise is the United Kingdom and the EU, after the settlement of the J&J arbitration (with the termination fight occasioned by the S-P reverse merger). We shall see, but it would seem that the past year's impressive growth in the Simponi®/Remicade® revenue stream (driven largely by EU growth) may be drawing to a gradual close. Here is PM Live! on it all:
. . . .In draft guidance the Institute says [Merck's] Remicade (Infliximab) and Simponi (golimumab), and AbbVie's Humira adalimumab) have not been proven to be more cost effective than current available treatments.[Ed. Note: Those being "biosimilars" (essentially generic biological agents) -- approved last summer -- and made by Celltrion, and Hospira.]
This is despite MSD agreeing a patient access scheme with the Department of Health to make a 100 mg dose of Simponi (which costs £1,525.94) available to the NHS at the same cost as the 50 mg dose (£762.97).
Including the patient access scheme and assuming the recommended dosage is followed, the cost of Simponi induction therapy is £2,289 and its monthly cost for maintenance therapy is £763.
Meanwhile, the cost of Remicade induction therapy at its recommended dose is £5,035 and the monthly cost of maintenance therapy is £210 and induction therapy with Humira costs £2,113 and it has a monthly cost for maintenance therapy of £704. . . .
Obviously, the EU biosimilar approvals of last year (see archive graphic, at right) are taking hold in the minds of the reimbursement crowd in the United Kingdom, and soon -- the EU, I predict. Do stay tuned.
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