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Eli Lilly’s Tirzepatide Receives the US FDA’s Fast Track Designation for the Treatment of Obesity

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Eli Lilly’s Tirzepatide Receives the US FDA’s Fast Track Designation for the Treatment of Obesity

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  • The US FDA has granted FTD to tirzepatide for obesity, or overweight with weight-related comorbidities. The P-III (SURMOUNT-1) trial evaluates tirzepatide (5/10/15mg) vs PBO in a ratio (1:1:1:1) in 2539 adult patients without T2D across the US, Argentina, Brazil, China, India & other countries
  • The co-primary objectives of the study showed that tirzepatide (10/15mg) was superior in the percentage of body weight reductions from baseline and patients achieved ≥5% body weight reduction @72wk. The P-III (SURMOUNT-2) are expected to complete at the end of April 2023
  • The company plans to initiate a rolling submission of NDA for tirzepatide for obesity or overweight in 2022, based on 2 P-III (SURMOUNT-1 & 2) trial results

Ref: PRNewswire | Image: Eli Lilly

Click here to­ read the full press release 

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Neha is a Senior Editor at PharmaShots. She is passionate and very enthusiastic about recent updates and developments in the life sciences and pharma industry. She covers Biopharma, MedTech, and Digital health segments along with different reports at PharmaShots. She can be contacted at connect@pharmashots.com.

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