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Completed Phase 2 Interventional

A Study Evaluating Safety and Efficacy of BIOD-123 Compared to Insulin Lispro (Humalog®)

ClinicalTrials.gov ID: NCT01686620

Public ClinicalTrials.gov record NCT01686620. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 3, 2026, 9:30 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Parallel Group Trial Evaluating Safety and Efficacy of BIOD-123 Compared to Insulin Lispro (Humalog®) in Subjects With Type 1 Diabetes Using Basal-bolus Insulin Injection Therapy

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT01686620
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Biodel
Industry
Enrollment
132 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 31, 2012
Primary completion
May 31, 2013
Completion
May 31, 2013
Last update posted
Jul 27, 2015

2012 – 2013

United States locations

U.S. sites
34
U.S. states
16
U.S. cities
31
Facility City State ZIP Site status
Anaheim Clinical Trials, LLC Anaheim California 92801
Profil Research Institute Chula Vista California 91911
John Muir Physician Network Clinical Research Center Concord California 94520
Scripps Whittier Diabetes Institute La Jolla California 92037
Private Practice - Richard Cherlin, MD. Los Gatos California 95032
Providence Clinical Research Pharmaseek North Hollywood California 91606
Monteagle Medical Center San Francisco California 94110
Mills-Peninsula Health Services San Mateo California 94401
The Center for Diabetes and Endocrine Care Hollywood Florida 33021
University of Miami Diabetes Research Institute Miami Florida 33136
Progressive Medical Research Pharmaseek Port Orange Florida 32127
Atlanta Diabetes Associates Atlanta Georgia 30309-1764
Endocrine Research Solutions Roswell Georgia 30076
Rocky Mountain Diabetes and Osteoporosis Center PA Idaho Falls Idaho 83404
MidAmerica Diabetes Associates, PA Wichita Kansas 67226
Kentucky Diabetes Lexington Kentucky 40503
Diabetes & Glandular Disease Research Rockville Maryland 20852
Henry Ford Health System Detroit Michigan 48235
Mercury Street Medical Butte Montana 59701
Desert Endocrinolgy Henderson Nevada 89052
Research Foundation of SUNY Upstate Medical University Syracuse New York 13210
Diabetes & Endocrinology Consultants, PC Morehead City North Carolina 28557
Sentral Clinical Research Services, LLC Cincinnati Ohio 45236
Oregon Health Sciences University Portland Oregon 97239
Texas Diabetes and Endocrinology Austin Texas 78731
Mountain Diabetes & Endrocrine Center Dallas Texas 28803
Dallas Diabetes and Endocrine Research Center Dallas Texas 75006
Research Institute of Dallas Dallas Texas 75231
Baylor Endocrine Center Dallas Texas 75246
Texas Diabetes and Endocrinology Round Rock Texas 78681
Sonterra Clinical Research San Antonio Texas 78258
Capital Clinical Research Center Olympia Washington 98502
Ranier Clinical Research, Inc Renton Washington 98507
Rockwood Clinic Spokane Washington 99202

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01686620, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 27, 2015 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01686620 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →