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CompletedNCT00367445Updated Jan 29, 2008

A Clinical Trial Comparing Short-Term Efficacy and Safety of Exubera and Lantus

A Phase 4 interventional study of Inhaled Human Insulin (Exubera) and Insulin Glargine (Lantus) in Diabetes Mellitus, Type 2, sponsored by Pfizer. Completed at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2008-01-29.

Sponsored by Pfizer · Phase 4, Interventional, and Treatment

Phase
Phase 4
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

To compare short-term efficacy and safety of Exubera vs Lantus in patients with type 2 diabetes mellitus

02

Conditions studied

  • Diabetes Mellitus, Type 2
03

In context

Diabetes Mellitus

10,925 studies on the registry are indexed under Diabetes Mellitus; 1,319 are open to participants now.

This study's enrollment of 30 is below the median of 80 across 8,367 interventional studies indexed under Diabetes Mellitus.

Browse Diabetes Mellitus studies →

Lead sponsor

Pfizer is the lead sponsor of 3,244 studies on the registry; 139 are open to participants now.

Of its 582 completed or terminated interventional studies of FDA-regulated products, 381 (65%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Diabetes mellitus Type 2

Exclusion criteria

Exclusion Criteria:

  • Severe Asthma, severe COPD
  • Smoking
05

Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
30 participants

Interventions

  • DrugInhaled Human Insulin (Exubera)
  • DrugInsulin Glargine (Lantus)
06

What researchers measure

Primary outcomes

  1. Variability of blood glucose over a period of 72 hours

Secondary outcomes

  1. Insulin pharmacokinetics

07

Study locations

1 site
  • Pfizer Investigational Site
    Chula Vista, California, United States
08

References and documents

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 29, 2008, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00367445
Lead sponsor
Pfizer
First posted
Aug 22, 2006
Start date
Sep 2006
Completion
Feb 2007
Last update
Jan 29, 2008

Study contacts

Pfizer CT.gov Call Center
study director · Pfizer
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jan 2008. You cannot join it, but the record below documents what was studied.

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