Zealand Pharma Boehringer Receives FDA Breakthrough Therapy Designation For Survodutide

T-Reuters10-08

Zealand Pharma A/S :Boehringer Receives Fda Breakthrough Therapy Designation For Survodutide.Fda Designation Based On Phase Ii Results For Survodutide.Boehringer Launches Two Phase Iii Studies For Survodutide.Liverage-Cirrhosis Primary Endpoint: All-Cause Mortality Or Liver Events.

Disclaimer: Investing carries risk. This is not financial advice. The above content should not be regarded as an offer, recommendation, or solicitation on acquiring or disposing of any financial products, any associated discussions, comments, or posts by author or other users should not be considered as such either. It is solely for general information purpose only, which does not consider your own investment objectives, financial situations or needs. TTM assumes no responsibility or warranty for the accuracy and completeness of the information, investors should do their own research and may seek professional advice before investing.

Comments

We need your insight to fill this gap
Leave a comment