drugset / Trial / NCT00327626
Safety, Tolerability, and Activity of ISIS 113715 in People With Type 2 Diabetes Mellitus Being Treated With Sulfonylurea
RandomizedParallel-groupDouble-blindTreatment
Summary
The aim of this study is to evaluate the safety, tolerability, and pharmacokinetics of two ISIS 113715 subcutaneous doses (15 mg and 30 mg/day) in combination with oral antidiabetic agents (OAD) versus OAD + placebo in patients with inadequately controlled type 2 diabetes, despite ongoing maximal treatment with OAD.
Timeline
- Start
- 2006-05-01
- Primary completion
- 2007-02-01
- Completion
- 2007-03-01
Outcome
Outcome not reported
Stopped: “study was never started due to regional geopolitical conflict”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | ISIS 113715 | Antisense oligonucleotide | 15 mg | Subcutaneous |
| Subject | ISIS 113715 | Antisense oligonucleotide | 30 mg | Subcutaneous |