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The approval was supported by liver biopsybased histological assessments from the first 800 patients after 72 weeks of treatment: Primary Endpoint 1: Resolution of steatohepatitis with no worsening of liver fibrosis Semaglutide group: 62.9% achieved the endpoint Placebo group: 34.3% achieved the endpoint Primary Endpoint 2: Improvement in liver fibrosis with no worsening of steatohepatitis Semaglutide group: 36.8% achieved the endpoint Placebo group: 22.4% achieved the endpoint Figure 1

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The easier the device is to understand and the more uniform the delivery systems become, the more comfortable will the doctors be in prescribing them and the more confident the patients using them a key factor in the next phase of Indias obesity and diabetes treatment journey