Drugs / Insulin degludec/liraglutide
Regulatory milestones approvals, filings & regulatory actions · 1 recorded
| Milestone | Jurisdiction | Brand | Indication | Date | Sentence it was read from |
|---|---|---|---|---|---|
| Filed | EU (EMA) | — | type 2 diabetes mellitus | 2013-05-31 | “Novo Nordisk today announced the submission to the European Medicines Agency of the marketing authorisation application for the approval of IDegLira” novonordisk.com ↗ “virksomheden har indsendt ansøgning om markedsføringstilladelse til Det Europæiske Lægemiddelagentur med henblik på godkendelse af IDegLira” novonordisk.com ↗ |
Trials 1
| Phase | Registry id | Dates | Indication | Sponsor | Status | Outcome |
|---|---|---|---|---|---|---|
| Phase 3 | NCT02911948 | Sep 2016 → Nov 2017 | type 2 diabetes mellitus | Novo Nordisk A/S | Completed | Met primary |
News releases announcing trial results or a regulatory action · 1
| Date | Issuer | Release |
|---|---|---|
| 2016-11-21 | Novo Nordisk A/S | Regulatory Novo Nordisk receives US FDA approval for Xultophy® 100/3.6 novonordisk.com ↗
Bagsværd, Denmark, 21 November 2016 - Novo Nordisk today announced that the US Food and Drug Administration (FDA) has approved the New Drug Application (NDA) for Xultophy® 100/3.6. |
All press releases naming this drug 15 releases
Evidence & citations 2 cited values
Every value below carries the sentence it was read from. 2 sources stand behind the page.
| Field | Value | Cited text |
|---|---|---|
| Known as | Insulin degludec/liraglutide | ClinicalTrials.gov intervention name — accepted as the source's own label NCT02911948 ↗ |
| Known as | IDegLira | “AIMS/INTRODUCTION: To assess efficacy and safety of insulin degludec/liraglutide (IDegLira) in Japanese participants with type 2 diabetes across different baseline characteristics.” PMID 33595901 ↗ Mar 2021 |