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Julia Moore Vogel, senior program director at the Scripps Research Translational Institute, noted that LoCITT enables even patients with the most severe symptoms to join the search for answers. Vogel, who has long COVID, and Eric Topol are co-principal investigators of the study

The observation of these distinct adverse events, not prominent in initial trials, underscores the critical role of ongoing postmarketing surveillance and adverse event reporting in fully characterizing a drug's safety profile in a broader patient population

Usually, the dose wont be raised to more than 15 mg per week

A pivotal strategic decision for manufacturers will be the choice of presentation: whether to offer the product in prefilled pens, multidose vials, or oral formulations where feasible