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DTP I is responsible for facilitating pre-application development of generic drugs by conducting and promoting regulatory science research to establish standards to ensure therapeutic equivalence of new generic drug products

June 17, 2025 Editor's Note: This story was updated to reflect new information about the federal approval of Wegovy to treat patients with MASH

Johns Hopkins University, Baltimore, MD

*Eligible patients with a BMI of 30, or 27 with comorbidities, lost an average of 19% of their body weight (-33.6 lbs) in a 68-week clinical trial evaluating 2.4 mg semaglutide, when combined with a reduced-calorie diet and increased physical activity

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