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Trials / Terminated

TerminatedNCT01785771

A Study to Evaluate ITCA 650 for the Treatment of Type 2 Diabetes in Patients With High Baseline HbA1c

An Open-Label Multi-Center Sub-Study to Evaluate the Efficacy, Safety and Tolerability of ITCA 650 in Patients With Type 2 Diabetes With High Baseline HbA1c

Status
Terminated
Phase
Phase 3
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
Intarcia Therapeutics · Industry
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

An 39-week plus extensions, open-label study to estimate the reduction in HbA1c in patients with initial HbA1c \>10% \</=12% who are treated with ITCA 650 20 mcg/day for 13 weeks followed by ITCA 650 60 mcg/day for 26 weeks plus optional 26-week extensions with continued treatment with ITCA 650 60 mcg/day

Conditions

Interventions

TypeNameDescription
DRUGITCA 650 (exenatide in DUROS)

Timeline

Start date
2013-05-01
Primary completion
2018-01-01
Completion
2018-01-01
First posted
2013-02-07
Last updated
2019-03-07

Locations

51 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01785771. Inclusion in this directory is not an endorsement.

A Study to Evaluate ITCA 650 for the Treatment of Type 2 Diabetes in Patients With High Baseline HbA1c (NCT01785771) · Clinical Trials Directory