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Also, in the COVID Group, the sed rate was markedly elevated, and all of them, five of them had pneumonia

Currently on FDA Category 2 with a PCAC review scheduled for July 2026

The clinical methodology was appropriate for an obesity drug: randomized, double-blind, placebo-controlled, multicenter designs with body-weight and body-composition endpoints, supported by dedicated safety, tolerability, and pharmacokinetic studies

We also evaluate liver and kidney function before and during therapy, since impaired metabolism can heighten the risk of adverse effects

Differences in P-glycoprotein activity in human and rodent bloodbrain barrier assessed by mechanistic modelling