The Effectivity and Safety Study of rExenatide-4 in Chinese Type 2 Diabetes Mellitus
NCT03239119 on ClinicalTrials.gov · last registry update 2017-08-03
456 participants. Its estimated completion date, 30 December 2018, has passed with no update to the record. Primary outcome, as filed: Change in HbA1c from Baseline to Week 30. A lapsed estimate is not a result and not a failure — sponsors are slow to refile — but ClinicalTrials.gov marks it nowhere on the record, so it is noted here. exenatide 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.
- Status
- UNKNOWN
- Phase
- P3
- Drug
- exenatideBydureon, Byetta
- Sponsor
- CSPC ZhongQi Pharmaceutical Technology Co., Ltd.
- Sponsor type
- Industry
- Enrollment
- 456
- Started
- 2017-11-30
- Primary completion
- 2018-12-30 estimated
Observed history
No changes recorded since monitoring began on 2026-08-21. This record has held steady. If a reporting date moves, a status changes or enrollment is resized, it will appear here with the previous value alongside the new one.
Primary outcome
Change in HbA1c from Baseline to Week 30
Conditions studied
Type2 Diabetes Mellitus
Every field above is taken directly from the registry record. See all detected changes across the class, or the exenatide page for this molecule’s full trial and approval history.