Drugs / insulin degludec/liraglutide
Regulatory milestones approvals, filings & regulatory actions · 2 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 ↗ |
| Filed | US (FDA) | — | type 2 diabetes mellitus | — | “IDegLira was submitted to the FDA in September 2015 under the US FDA's Prescription Drug User Fee Act V (PDUFA V) regulation.” novonordisk.com ↗ |
Trials 1
| Phase | Registry id | Dates | Indication | Sponsor | Status | Outcome |
|---|---|---|---|---|---|---|
| Phase 3 | NCT02773368 | May 2016 → Sep 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 ↗
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 3 cited values
Every value below carries the sentence it was read from. 1 source stands behind the page.
| Field | Value | Cited text |
|---|---|---|
| Known as | insulin degludec/liraglutide | ClinicalTrials.gov intervention name — accepted as the source's own label NCT02773368 ↗ |
| Known as | IDegLira | “insulin degludec/liraglutide (IDegLira)” NCT02773368 ↗ |
| Route | Subcutaneous | “IDegLira will be given subcutaneously ( s.c., under the skin) once daily.” NCT02773368 ↗ |