Clinical trial
A Study for Patients With Type 2 Diabetes Mellitus
NCT00490854 · Eli Lilly and Company, Industry · Completed
Key facts
| NCT number | NCT00490854 |
|---|---|
| Title | A Study for Patients With Type 2 Diabetes Mellitus |
| Official title | A Crossover Study to Evaluate the Efficacy and Safety of Preprandial Human Insulin Inhalation Powder (HIIP) Compared to Once-Daily NPH in Insulin-Naïve Patients With Type 2 Diabetes Mellitus on Oral Agents |
| Lead sponsor | Eli Lilly and Company, Industry |
| Collaborators | Alkermes, Inc. Industry |
| Status | Completed |
| Phase | Phase 2/Phase 3 |
| Study type | Interventional |
| Conditions | Diabetes Mellitus, Type 2 |
| Intervention type | Drug |
| Interventions | Human Insulin Inhalation Powder, Neutral protamine hagedorn insulin |
| Enrollment | 129 |
| Start date | Jul 1, 2007 |
| Primary completion | May 1, 2008 |
| Completion | May 1, 2008 |
| First posted | Jun 25, 2007 |
| Last update posted | Jul 10, 2008 |
| Countries | Japan |
At a glance
- 10–99 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: