Boehringer Ingelheim USA Corporation

🇺🇸United States
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pipelinereview.com
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Boehringer receives U.S. FDA Breakthrough Therapy designation and initiates two phase III

Boehringer Ingelheim receives FDA Breakthrough Therapy designation for survodutide, a dual glucagon/GLP-1 receptor agonist, for treating non-cirrhotic MASH with moderate or advanced fibrosis. Two Phase III studies, LIVERAGE and LIVERAGE-Cirrhosis, are initiated to assess survodutide's efficacy in MASH patients with fibrosis and cirrhosis, respectively.
pharmacytimes.com
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FDA Grants Survodutide Breakthrough Therapy Designation for Treatment of Adults With MASH

Survodutide (BI 456906) received FDA breakthrough therapy designation for non-cirrhotic MASH and moderate/advanced fibrosis. Based on LIVERAGE study results, survodutide showed significant improvements in MASH and liver fat reduction, though with higher adverse effects like nausea and diarrhea.
pharmexec.com
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FDA Grants Breakthrough Therapy Designation to Boehringer Ingelheim's Survodutide for ...

FDA grants Breakthrough Therapy designation to Boehringer Ingelheim’s survodutide for MASH and moderate to advanced fibrosis. Two Phase III trials, LIVERAGE and LIVERAGE-Cirrhosis, will evaluate its efficacy and safety. Survodutide aims to address the significant medical need for MASH treatment.

Boehringer kickstarts two Phase III trials as MASH therapy wins breakthrough status

Boehringer Ingelheim received FDA breakthrough therapy designation for survodutide, a dual GLP-1 and glucagon receptor agonist, for treating non-cirrhotic MASH and moderate or advanced fibrosis. The company initiated two Phase III trials, LIVERAGE and LIVERAGE-Cirrhosis, evaluating survodutide in MASH patients with moderate or advanced fibrosis and cirrhosis, respectively. The MASH market is projected to reach $25.7bn by 2032.
quantisnow.com
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Zealand Pharma announces that Boehringer receives U.S. FDA Breakthrough Therapy

Zealand Pharma reports Boehringer Ingelheim's U.S. FDA Breakthrough Therapy designation for survodutide in treating non-cirrhotic MASH and moderate or advanced fibrosis. Boehringer initiates two Phase III trials, LIVERAGE and LIVERAGE-Cirrhosis, for survodutide in MASH patients with fibrosis stages 2 or 3 and cirrhosis stage 4, respectively.
kfgo.com
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Zealand, Boehringer win FDA breakthrough status to treat fatty liver

Denmark’s Zealand Pharma and German partner Boehringer Ingelheim win U.S. FDA Breakthrough Therapy for review of experimental weight-loss drug survodutide, targeting non-cirrhotic metabolic dysfunction-associated steatohepatitis (MASH). Two survodutide studies initiated in final human testing stages for MASH and liver scarring treatment.
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