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By the early 2020s, it held over 200 patents related to Humira, with expiration dates stretching to 2034 [16]

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Group III: reserpine + low dose of semaglutide (Res + LD of Sema group), Group IV: reserpine + intermediate dose of semaglutide (Res + ID of Sema group), and Group V: reserpine + high dose of semaglutide (Res + HD of Sema): reserpine (1 mg/kg/day) was subcutaneously administered into rats for 3 successive days, then they were daily injected with intraperitoneal low (5 nmol/kg), intermediate (10 nmol/kg) (Yang et al