Status:
COMPLETED
An Open Label, Multi-Center, Follow-on Study Examining the Long-Term Safety and Efficacy of Insulin VIAject™ in Subjects With Type 2 Diabetes Mellitus
Lead Sponsor:
Biodel
Conditions:
Diabetes Mellitus
Eligibility:
All Genders
30-70 years
Phase:
PHASE3
Brief Summary
Follow-on study to the VIAject™-08J study to evaluate the long-term safety and efficacy of VIAject™ when used as prandial insulin in combination with Lantus® in subjects with type 2 diabetes mellitus....
Eligibility Criteria
Inclusion
- Completed the VIAject™-08J protocol
- Informed consent must be obtained in writing for all subjects.
Exclusion
- History of frequent severe hypoglycemia within the prior six months which prevent study participation at the discretion of the investigator
- History of known hypersensitivity to any of the components in the study medication
- Progressive disease likely to prove fatal
- Known significant hepatic disease or serum AST or ALT values \> 3 times the upper limit of normal or bilirubin levels \> 1.5 times the upper limit of normal
- Severe complications of diabetes mellitus including a history or finding of Stage III or IV diabetic retinopathy (see Appendix B), proteinuria \> 2+ by urine dipstick, serum creatinine of \>1.8 mg/dl for males or \>1.5 mg/dl for females, history of renal transplant, severe peripheral vascular disease, which has resulted in amputation or recent onset of chronic foot ulcers or claudication, or the recent, clinically documented loss a pedal pulse.
- History of moderate to severe ketoacidosis within the 3 months preceding screening for the study
- Current drug or alcohol abuse, or a history which in the opinion of the Investigator will impair subject safety or protocol compliance.
- Current significant cardiovascular, respiratory, gastrointestinal, hepatic, renal, neurological, psychiatric and/or hematological disease as evaluated by the Investigator
- A sexually active woman of childbearing age not actively and consistently practicing birth control by using a medically accepted device or therapy or a woman intending to become pregnant during the study
- Abnormal ECG, safety lab or physical examination results which, in the opinion of the investigator, render the participation of the subject in the study to be inappropriate or unsafe
- A history of lack of compliance with medical instructions, recent drug or alcohol abuse, or other reasons which, in the opinion of the investigator, render the participation of the subject in the study to be inappropriate or unsafe
Key Trial Info
Start Date :
July 1 2007
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 1 2010
Estimated Enrollment :
116 Patients enrolled
Trial Details
Trial ID
NCT00875108
Start Date
July 1 2007
End Date
January 1 2010
Last Update
July 29 2015
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