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 | “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 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 | NCT01952145 | Sep 2013 → Nov 2014 | type 2 diabetes mellitus | Novo Nordisk A/S | Completed | Met primary |
Press releases naming this drug 14 releases
Evidence & citations 3 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 NCT01952145 ↗ |
| Known as | IDegLira | “This study assessed the efficacy of insulin degludec/liraglutide (IDegLira) vs insulin glargine U100 (IGlar) across categories of baseline glycated haemoglobin” PMID 28643425 ↗ Jul 2017 |
| Route | Subcutaneous | “Insulin degludec/liraglutide is injected subcutaneously s.c. (under the skin) once daily (OD).” NCT01952145 ↗ |