What happens next in GLP-1 — and when.

Trial results

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
exenatide
Bydureon, 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.

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