Create Account
Log In
Dark
chart
exchange
Premium
Terminal
Screener
Stocks
Crypto
Forex
Trends
Depth
Close
Check out our Level2View


Danish pharmaceutical company Novo Nordisk A/S (NVO) said Friday that it has resubmitted a label expansion application to the US Food and Drug Administration for the existing marketing authorization for Ozempic or semaglutide, a once-weekly glucagon-like peptide-1 (GLP-1) analogue, to introduce a new dose of 2.0 mg.


RTTNews | May 28, 2021 10:47AM EDT

10:46 Friday, May 28, 2021 (RTTNews.com) - Danish pharmaceutical company Novo Nordisk A/S (NVO) said Friday that it has resubmitted a label expansion application to the US Food and Drug Administration for the existing marketing authorization for Ozempic or semaglutide, a once-weekly glucagon-like peptide-1 (GLP-1) analogue, to introduce a new dose of 2.0 mg.

The re-submission follows the US Food and Drug Administration issued a Refusal to File letter on 22 March 2021 covering the label expansion application for once-weekly semaglutide 2.0 mg for the treatment of type 2 diabetes which was filed on 20 January 2021.

In the letter, FDA had requested additional information including data relating to a proposed new manufacturing site.

The standard review time by the FDA is 10 months.

Read the original article on RTTNews ( https://www.rttnews.com/3198460/novo-nordisk-resubmits-semaglutide-2-0-mg-for-treatment-of-type-2-diabetes-for-us-approval.aspx)

For comments and feedback: contact editorial@rttnews.com

Copyright(c) 2021 RTTNews.com All Rights Reserved






Share
About
Pricing
Policies
Markets
API
Info
tz UTC-4
Connect with us
ChartExchange Email
ChartExchange on Discord
ChartExchange on X
ChartExchange on Reddit
ChartExchange on GitHub
ChartExchange on YouTube
© 2020 - 2025 ChartExchange LLC