AbbVie has been granted a patent for a method of treating active psoriatic arthritis by administering a tablet containing a specific compound once daily. The compound, (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide, is administered in a 15 mg dose. GlobalData’s report on AbbVie gives a 360-degree view of the company including its patenting strategy. Buy the report here.
According to GlobalData’s company profile on AbbVie, Peptide pharmacophores was a key innovation area identified from patents. AbbVie's grant share as of May 2024 was 40%. Grant share is based on the ratio of number of grants to total number of patents.
Treatment of psoriatic arthritis with tablet containing compound 1
A recently granted patent (Publication Number: US11993605B2) discloses a method for treating active psoriatic arthritis in human patients. The method involves orally administering a tablet containing a specific compound, (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide (Compound 1), at a therapeutically effective amount of 15 mg once daily. This treatment is intended for adult patients who have shown inadequate response or intolerance to disease-modifying antirheumatic drugs, methotrexate, or anti-TNF biologic agents.
Furthermore, the patent claims that administering the specified compound at the mentioned dosage results in significant clinical responses. The method aims to achieve an ACR70, ACR50, or ACR20 response at 12 weeks after the initial daily administration of the tablet. These responses indicate varying levels of improvement in the patient's condition, with the ACR70 response being the most substantial. The compound is administered in the form of 15.4 mg of Freebase Hydrate Form C, ensuring optimal therapeutic efficacy in treating active psoriatic arthritis in patients who have not responded well to conventional treatments.
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