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Standard titration protocol from clinical trials The Phase 2 NEJM trial used the following escalation schedule for the 12 mg dose group: Weeks 1 through 4: 2 mg once weekly (subcutaneous) Weeks 5 through 8: 4 mg once weekly Weeks 9 through 12: 8 mg once weekly Week 13 and beyond: 12 mg once weekly (maintenance dose) For the 8 mg target dose, the schedule was: Weeks 1 through 4: 2 mg once weekly Weeks 5 through 8: 4 mg once weekly Week 9 and beyond: 8 mg once weekly (maintenance dose) These titration schedules are not suggestions

10.1016/s0306-4522(97)00252-2 Neuroscience 41 FurutaA.RothsteinJ

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In addition, the increase in Parasutterella after IL-17A inhibitor therapy may be related to the development of inflammatory bowel disease in some PSO patients (97), as higher levels of Parasutterella are associated with chronic inflammation in Irritable Bowel Syndrome (IBS) (98)

Treatment of 48 cases of restless legs syndrome with dermal needle therapy