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The study enrolled 36 healthy adults (age 45-65) and administered sermorelin via three routes in randomized order with 2-week washout periods: 300 mcg subcutaneous injection 1500 mcg sublingual tablet (5x the injection dose to attempt bioavailability compensation) Placebo Blood samples were drawn at baseline, 30 minutes, 60 minutes, 90 minutes, and 120 minutes

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