Logos are each company's own site icon, matched by name through Wikidata.Company names and logos identify the companies in public FDA and registry records and do not imply endorsement.
Sold as Adlyxin. Every FDA application for this active ingredient.
As of Nov 14, 2026, FDA lists 1 application for Lixisenatide (sold as Adlyxin), first approved Jul 27, 2016, with 1 new use approved and 0 published complete response letters.
First approved in Japan 37 months before the US. PMDA's English list since 2008, matched by ingredient; see all Japanese approvals
LyxumiaA drug with a revised indication for the treatment of type 2 diabetes mellitus. · Sanofi K.K. · Dec 19, 2016
Lyxumia, new ingredientA drug with a new active ingredient indicated for the treatment of type 2 diabetes mellitus (for use only in patients who have not responded sufficiently to… · Sanofi K.K. · Jun 28, 2013 · Review report
Clinical Trials
8 open or ongoing studies name this ingredient as an intervention, including as a comparator; newest first. See all
Applications, approvals and products come from FDA's Drugs@FDA data files, refreshed weekly, grouped by active ingredient as FDA spells it. Complete response letters are FDA's published letters. Medicare spending is CMS's Part D and Part B dashboard, matched to this ingredient by generic name; shortages are FDA's shortage list, matched by application number; clinical trials are ClinicalTrials.gov studies naming the ingredient as an intervention, refreshed daily; safety programs are FDA's REMS list, matched by application number or, for shared programs, by ingredient.Drugs@FDA
Sanofi-Aventis US