Efficacy and Safety of the Insulin Glargine/Lixisenatide Fixed Ratio Combination (LixiLan) to Insulin Glargine Alone on Top of Oral Anti-diabetic Drugs (OADs) With Type 2 Diabetes in Japan
NCT02752828 on ClinicalTrials.gov · last registry update 2020-06-16
Finished 12 March 2018, after enrolling 521 people. Primary outcome, as filed: Change from baseline in HbA1c. lixisenatide is already approved in the US for type 2 diabetes, so this is asking a further question rather than establishing the drug works at all. The registry entry has been edited 1 time since then.
- Status
- COMPLETED
- Phase
- P3
- Drug
- lixisenatideSoliqua, Adlyxin
- Sponsor
- Sanofi
- Sponsor type
- Industry
- Enrollment
- 521
- Started
- 2016-05-23
- Primary completion
- 2018-03-12 actual
Observed history
Every change this record has made since we started watching it. ClinicalTrials.gov shows only the current value. When a field is edited the previous one is overwritten and nothing is published to say so, so this history exists only because someone was recording it at the time.
| Detected | Change | Detail |
|---|---|---|
| 2026-08-21 | First seen in registry | Registered as COMPLETED, P3 |
Primary outcome
Change from baseline in HbA1c
Conditions studied
Type 2 Diabetes Mellitus
Every field above is taken directly from the registry record. See all detected changes across the class, or the lixisenatide page for this molecule’s full trial and approval history.