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Strategies to facilitate medication adherence, persistence and treatment intensification in people with T2D should be made a priority in order to achieve and maintain glycaemic targets and improve outcomes in this population

Pfizers dose-optimization studies of once-daily formulations of danuglipron ( NCT06567327 and NCT06568731 ) met key pharmacokinetic objectives and confirmed a formulation and dose with the potential to deliver a competitive efficacy and tolerability profile in Phase 3 testing, based on earlier studies of twice-daily danuglipron

This means that FDA does not verify the safety, effectiveness or quality of compounded drugs before they are marketed.

Propensity score matching (PSM) with 1:1 ratio was employed to create balanced cohorts

Refills announces its clinician-led telehealth platform offering GLP-1 weight loss treatments and everyday health solutions