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[119] conducted a phase II clinical trial in patients with NASH, that is, a placebo-controlled trial of subcutaneous sommarutide in the treatment of NASH, and found that sommarutide treatment resulted in a significantly higher proportion of patients in remission of NASH compared with placebo

This formulation is commonly prescribed as a starting dose to help patients gradually adjust to semaglutide therapy while minimizing gastrointestinal side effects

From there, titrate up by 2.5 mg increments every 4 weeks based on tolerance and results

Coloration is shiny black with thin transversal yellow bands, often broken on top of back and wider near belly