Complaints Associated With Use of Pre-Filled Pen B With Type 2 Diabetics on Twice-Daily Insulin
Completed · Phase 3
Conditions studied: Type 2 Diabetes Mellitus
In brief
Trial of new insulin injection pen called Pre-filled Pen B by type 2 diabetics in take home situations. Patients must use insulin lispro injection \[rDNA origin\] Low Mix twice daily during the trial.
Key facts
- Study ID
- NCT00231725
- Run by
- Eli Lilly and Company
- People needed
- 370
- Starts
- 2005-09-01
- Expected to finish
- 2006-04-01
- Last updated by the study team
- 2007-06-27
Who can join
Age: 25 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Type 2 Diabetes
- Already on Lilly insulin or beginning insulin therapy
- 25 to 75 years old inclusive
You may not qualify if…
- Currently using, or had used during previous month, oral diabetes medication that is NOT approved for use in combination with insulin in patient's country
- More than 3 unexplained episodes of severe hypoglycemia within 6 months prior to trial
Where it is running
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician. — Memphis, Tennessee, United States
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician. — Pamplona, Spain
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician. — Requena, Spain
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician. — Middlesbrough, United Kingdom
Full record on ClinicalTrials.gov
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