A Study to Evaluate ITCA 650 Compared to Sitagliptin as add-on Therapy for the Treatment of Type 2 Diabetes

NCT01455870 on ClinicalTrials.gov · last registry update 2016-06-02

Finished July 2015, after enrolling 535 people. Primary outcome, as filed: Change in HbA1c between Week 52 and Day 0. 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: COMPLETED
Phase: P3
Drug: exenatide
Bydureon, Byetta
Sponsor: Intarcia Therapeutics
Sponsor type: Industry
Enrollment: 535
Started: 2013-05
Primary completion: 2015-07 actual

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 between Week 52 and Day 0

Conditions studied

Type 2 Diabetes

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.