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Briefly, the scores of six predetermined segments (scored from 0 to 3 in each segment) were assessed according to the amount of clotted subarachnoid blood

The biopharma is also studying MET-233i in phase I trials as a monotherapy and it has a further two oral GLP-1 RA candidates that are expected to begin clinical trials soon

Under standard review timelines, that places potential FDA approval somewhere around mid to late next year

Randomization The randomization was done using a computer-generated random number sequence

Overall, the findings provide cautious, low-certainty reassurance regarding inadvertent maternal exposure, particularly during early pregnancy, but do not establish that these drugs are safe for routine use throughout pregnancy