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The FDA requires generic applicants to demonstrate bioequivalence through clinical studies, adding years and millions of dollars to the approval timeline

Volunteering an accurate picture of your intake lets your prescriber give relevant advice about timing, hypoglycemia risk, and whether your symptoms have an explanation beyond the medication itself

Informed consent was obtained prior to the study

Clinical data supports visceral fat reduction in non-HIV obese populations, including the 2014 JAMA trial by Stanley and colleagues

Accumulated evidence shows that IGF-1 can be an effective option in the treatment of this prevalence-increasing condition, as we shall further explain in detail

Novo will also handle clinical development through commercialization