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Completed Phase 2 Interventional

A Study Comparing the Pharmacodynamic Properties of Insulin VIAJECT™, Regular Human Insulin, and Insulin Lispro

ClinicalTrials.gov ID: NCT01000922

Public ClinicalTrials.gov record NCT01000922. 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 May 6, 2026, 5:29 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 Single Center, Randomized, Open-Label, Crossover Study, Comparing the Pharmacodynamic Properties of Insulin VIAJECT™, Regular Human Insulin, and Insulin Lispro Either in Combination With a Basal Insulin Infusion or With Insulin Glargine Relative to a Standardized Meal in Patients With Type 1 Diabetes

Study identification

NCT ID
NCT01000922
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Biodel
Industry
Enrollment
24 participants

Conditions and interventions

Interventions

  • Insulin Glargine/VIAject Drug
  • Lispro Drug
  • Regular Human Insulin Drug
  • VIAject Drug
  • VIAject 50% Drug
  • VIAject/Insulin Glargine Drug

Drug

Eligibility (public fields only)

Age range
19 Years to 70 Years
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
May 31, 2006
Primary completion
Dec 31, 2007
Completion
Dec 31, 2007
Last update posted
Jul 28, 2015

2006 – 2008

United States locations

U.S. sites
1
U.S. states
1
U.S. cities
1
Facility City State ZIP Site status
Profil Institute for Clinical Research, Inc. (PICR) Chula Vista California 91911

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 NCT01000922, 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 28, 2015 · Synced May 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01000922 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →