Visiting from the United States? GLPInfo has a North American edition with US channels and dollar prices: open the US edition. Canada follows in a later release.

Medicine profile

Liraglutide

Once-daily GLP-1 receptor agonist; the first GLP-1 medicine licensed for weight management.

Generic name
Liraglutide
Also known as
Saxenda, Victoza
Sponsor and licensing
Novo Nordisk (originator)
Mechanism
GLP-1 receptor agonist
Molecular type
Peptide (mechanism and molecular type are recorded separately: GLP-1 activity does not make a medicine a peptide)

Brands, routes and formulations

Saxenda

subcutaneous 路 once-daily injection

  • United States: Chronic weight management (23 Dec 2014)

Victoza

subcutaneous 路 once-daily injection

  • United States: Type 2 diabetes (glycaemic control) (25 Jan 2010)

Regulatory status by jurisdiction

Authorisation, launch and funded access are three different things and are shown separately. "Not recorded" means GLPInfo has not verified an event, not that nothing has happened.

United States (FDA)United Kingdom (MHRA)European Union (EMA / EC)
Regulatory authorisation25 Jan 2010 路 VictozaType 2 diabetes (glycaemic control)23 Dec 2014 路 SaxendaChronic weight managementNot recordedNot recorded
Commercial launchNot recordedNot recordedNot recorded
Funded accessNot recordedNot recordedNot recorded

Development timeline

Liraglutide

Novo Nordisk 路 GLP-1 receptor agonist 路 Peptide
Region
201020112012201320142015201620172018201920202021202220232024202520262027202820292030
UKMHRA
No verified events yet
EUEMA / European Commission
No verified events yet
Confirmed eventCompany targetRegulator targetEditorial estimateTiming unknown or undatedSafety update

Dashed line: today, 13 Sep 2026. Future windows are conditional. Approval, launch and funded access are separate milestones.

Select a marker to open its record in the pipeline view, which has the detail panel and the accessible list.

Next milestone and forecast rationale

No forecast is published for Liraglutide. Approved medicines only carry forecasts for new indications or jurisdictions when a filing anchor exists.

Trial evidence

TrialPhasePopulationDurationResults
LEAD-3 MonoNovo Nordisk 路 subcutaneous, once daily3746 adults with early type 2 diabetes previously treated with diet and exercise or one oral medicine52 weeksOn file from the research workbook; withheld until the primary publication or registry record is attached.
SCALE Obesity and PrediabetesNovo Nordisk 路 subcutaneous, once daily33,731 adults without type 2 diabetes; BMI 30 or more, or 27 or more with hypertension or dyslipidaemia56 weeksOn file from the research workbook; withheld until the primary publication or registry record is attached.

GLPInfo does not rank unrelated trials against each other or quote "weight loss per week": populations, durations and methods differ and weight change is not linear. Results appear here per trial and dose arm, with comparator, endpoint and source, once cited.

Known limitations and official labels

This profile is assembled from the regulatory records and sponsor statements GLPInfo has verified; it is not a complete review of Liraglutide. The current official label in each jurisdiction is the authority on indications, populations and safety. Official records read for this profile: Drugs@FDA: NDA 206321 Saxenda (liraglutide) approval history; Drugs@FDA: NDA 022341 Victoza (liraglutide) approval history.

Review date and correction history

Records last checked 13 Sep 2026. No corrections have been made to the records on this profile; every record is at version 1. Report a correction.

Related news

No news articles yet for Liraglutide.

Follow Liraglutide All medicines