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Comparison · NCT00308737-291304f7

Technosphere® Insulin vs Usual Care: FEV1 Decrease of ≥ 15% From Baseline Value at Last Measurement for TI vs Usual Care

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Technosphere® Insulin vs Usual Care: FEV1 Decrease of ≥ 15% From Baseline Value at Last Measurement for TI vs Usual Care. Trial comparisons, record NCT00308737-291304f7. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00308737-291304f7

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.05750.04280.0769wilson
Risk in group 20.03280.02260.0473wilson
Risk difference, group 1 minus group 20.02480.004140.0466newcombe hybrid score
Risk ratio, group 1 over group 21.761.092.82log
Odds ratio, group 1 over group 21.81.12.95log
Number needed to treat, for one more participant with the outcome on Technosphere® Insulin than on Usual Care40.421.5242from the risk difference interval

Groups2

Group 2 names the comparator: usual care.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Technosphere® InsulinTechnosphere Insulin42730OG000
Group 2Usual CareUsual care27824OG001

Outcome

Type
PRIMARY
Title
FEV1 Decrease of ≥ 15% From Baseline Value at Last Measurement for TI vs Usual Care
Description
FEV1 decrease of ≥ 15% from Baseline value at last measurement
Time frame
Baseline to Month 24
Population
Intention to Treat (ITT)

Source ClinicalTrials.gov

Trial

Title
Safety of Inhaled Insulin With Type 1 and Type 2 Diabetes
NCT number
NCT00308737
Phases
PHASE3
Conditions
Diabetes, Type 1, Diabetes, Type 2
Interventions
Technosphere® Insulin Inhalation Powder, Usual Care
Lead sponsor
Mannkind Corporation
Results first posted
2014-10-16

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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