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Enrolled participants were randomized to receive 3 mg, 7 mg, or 14 mg of oral semaglutide or placebo once daily for 52 weeks
The DEA doesn't schedule it as a controlled substance, though FDA can pursue enforcement against therapeutic claims
Primer sequences are listed in Supplementary Table 1
However, not enough is known about this theoretical issue to elucidate a risk-benefit tradeoff and how timing of treatment works into such a tradeoff
Natl Med J India
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