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NCT01686620 · ClinicalTrials.gov registry record · Phase 2
A Study Evaluating Safety and Efficacy of BIOD-123 Compared to Insulin Lispro (Humalog®)
A Phase 2 study, sponsored by Biodel.
- Completed
- Registry status
- Phase 2
- Development phase
- 132
- Enrollment target
NCT01686620: Completed Phase 2 study, sponsored by Biodel.
NCT01686620 is a Phase 2 study that has completed, run by Biodel. The registered enrollment target is 132 participants, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01686620, a Phase 2 study, has completed, sponsored by Biodel.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 132 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate the safety and efficacy of BIOD-123 compared to insulin lispro (Humalog®) when used as part of a basal-bolus regimen in patients with type 1 diabetes.
Interventions
- DRUG BIOD-123
- DRUG Lispro (Humalog)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 132 participants |
| Start Date | 2012-08 |
| Est. Completion | 2013-06 |
| Phase | Phase 2 |
What the finished NCT01686620 record still lists
NCT01686620 is an interventional study that assigns participants to a tested intervention. The registered 132 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target.
The record links to 0 conditions, and to 2 interventions - of which BIOD-123 is the first listed.
NCT01686620 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01686620 about?
NCT01686620 is a clinical study titled "A Study Evaluating Safety and Efficacy of BIOD-123 Compared to Insulin Lispro (Humalog®)". The purpose of this study is to evaluate the safety and efficacy of BIOD-123 compared to insulin lispro (Humalog®) when used as part of a basal-bolus regimen in patients with type 1 diabetes.
What is the current status of trial NCT01686620?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 132 participants. The study started on 2012-08. Estimated completion is 2013-06.
What interventions are being tested in trial NCT01686620?
The interventions under investigation include: BIOD-123 (DRUG), Lispro (Humalog) (DRUG).
Who is sponsoring clinical trial NCT01686620?
This trial is sponsored by Biodel, which has 6 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01686620's enrollment target sits among peer trials
132 539th of 2000 higher than 1,460 of 2,000 other Phase 2 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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